No retraction, correction or concern found when last checked on Oct 18, 2026.
Risk Factors for Acute Leukemia in Children: A Review
Martin Belson, Beverely Kingsley, Adrianne Holmes
Environmental Health Perspectives · 2006 · Review · Public domain
Abstract
Although overall incidence is rare, leukemia is the most common type of childhood cancer. It accounts for 30% of all cancers diagnosed in children younger than 15 years. Within this population, acute lymphocytic leukemia (ALL) occurs approximately five times more frequently than acute myelogenous leukemia (AML) and accounts for approximately 78% of all childhood leukemia diagnoses. Epidemiologic studies of acute leukemias in children have examined possible risk factors, including genetic, infectious, and environmental, in an attempt to determine etiology. Only one environmental risk factor (ionizing radiation) has been significantly linked to ALL or AML. Most environmental risk factors have been found to be weakly and inconsistently associated with either form of acute childhood leukemia. Our review focuses on the demographics of childhood leukemia and the risk factors that have been associated with the development of childhood ALL or AML. The environmental risk factors discussed include ionizing radiation, non-ionizing radiation, hydrocarbons, pesticides, alcohol use, cigarette smoking, and illicit drug use. Knowledge of these particular risk factors can be used to support measures to reduce potentially harmful exposures and decrease the risk of disease. We also review genetic and infectious risk factors and other variables, including maternal reproductive history and birth characteristics.
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 18, 2026. Paragraph numbers are ours, so an answer can point at one.
Although overall incidence is rare, leukemia is the most common type of childhood cancer, accounting for 30% of all cancers diagnosed in children younger than 15 years. Within this population, acute lymphocytic leukemia (ALL) occurs approximately five times more frequently than acute myelogenous leukemia (AML) and accounts for approximately three-quarters of all childhood leukemia diagnoses. Chronic myeloid leukemias make up most of the other childhood leukemia cases. Childhood cases account for about 12% of all leukemias but make up > 60% of ALL cases.
In the United States, the incidence of childhood ALL increased between 1975 and 2002; however, this increase was not statistically significant. The observed increase may be due in part to changes in diagnostic practice and accuracy and improved reporting. The incidence rate of childhood ALL is now stable at three to four new cases per year per 100,000 children who are younger than 15 years, with a peak incidence at approximately 2–5 years of age. For childhood AML, the peak incidence rate occurs during the first year of life then decreases steadily through 4 years of age, where it remains relatively constant throughout childhood.
The incidence of ALL, particularly T-cell ALL, is slightly higher among boys than girls.. Girls, however, have a higher incidence of all leukemias during the first year of life. No differences in incidence of AML exist between girls and boys.
Throughout childhood, the incidence rate of ALL among African American children is approximately half the rate among Caucasian children. During the first few years of life, the incidence rate of AML among African American children is approximately one-third the rate among Caucasian children; however, African American children ≥ 3 years of age have higher rates than Caucasians.
Until the early 1980s, leukemia was the most common cause of death due to cancer among children in the United States. The mortality rate for all childhood leukemias decreased by 20% from 1975 through 1995, and the rate of children dying of leukemia has significantly decreased compared with the death rate from childhood brain tumors.
The overall cure rate for childhood ALL is now approximately 75–80%; however, for AML the cure rate is between 40 and 45%. In earlier large national trials, treatment results for African American children had not been as impressive as they were for Caucasian children. A recent study performed at St. Jude Children’s Hospital compared the clinical outcomes of therapy for African American and Caucasian children with ALL and concluded that with equal access to effective antileukemic therapy, children of both racial groups can expect the same high rate of ALL cure. However, another author concluded that ethnic or cultural differences in adherence to treatment have not been examined systematically in sufficiently large populations in the United States to draw meaningful conclusions regarding the impact of nonadherence on ethnic and racial differences in outcome of children with ALL.
Risk Factors
Epidemiologic studies of acute leukemias in children have examined a number of possible risk factors (e.g., environmental, genetic, or infectious) in an effort to determine the etiology of the disease. Only one environmental risk factor (ionizing radiation) has been significantly linked with either ALL or AML; most environmental risk factors [e.g., electromagnetic fields (EMFs), cigarette smoking] have been weakly or inconsistently associated with either form of childhood leukemia.
Because childhood leukemia is a rare occurrence, prospective studies are difficult to conduct, and therefore studies most frequently use a retrospective case–control design. Although easier to conduct, these studies have several inherent limitations. For example, bias may be introduced into a retrospective study because exposure is measured indirectly, is self-reported, and may be differentially recalled by parents of a well, versus a sick, child. Bias may also be introduced if a certain segment of the population does not respond to the study survey. Other limitations include a relatively small number of case children, the number of spurious results that arise from making many comparisons, and the questionable relevance of cross-sectional sampling after illness has developed, given the latency of the disease. Despite these limitations, results from epidemiologic research that identifies environmental risk factors for childhood leukemia can support measures to alleviate potentially harmful exposures and reduce the risk for disease.
The environmental risk factors we discuss in this article include some of the more researched and controversial topics including ionizing and nonionizing radiation, chemicals such as hydrocarbons and pesticides, alcohol, tobacco use, and illicit drug use. Knowledge of these particular risk factors can be used to support measures to alleviate potentially harmful exposures and reduce the risk of disease. We also review genetic and infectious risk factors and other variables, including maternal reproductive history and birth characteristics.
Ionizing radiation
Ionizing radiation is one of the few exposures for which the causal relationship with childhood leukemia, particularly AML, has been established. The magnitude of the risk depends on the dose of radiation, the duration of exposure, and the age of the individual at the time of exposure. Studies have demonstrated the relationship between the degree of irradiation and occurrence of leukemia. For example, leukemia rates among survivors who were within 1,000 m of the atomic bomb explosions at Hiroshima and Nagasaki, Japan, were 20-fold higher than rates among the general population (Mahoney 1955). The potential effect of ionizing radiation exposure on children may occur during preconception, pregnancy, or the postnatal period.
Paternal preconception exposure and close proximity to a nuclear facility
Numerous epidemiologic studies have investigated the potential association between childhood leukemia and paternal ionizing radiation exposure in the workplace before conception or preconception, also referred to as “preconception paternal irradiation” (PPI). Some studies have found an association, whereas others have not.
examined whether the observed excess of childhood leukemia was related to nearness to Sellafield nuclear plant in the West Cumbria district of the United Kingdom from 1950 to 1985. Relative risk was higher for leukemia in children born near Sellafield and for children of fathers employed at the plant at their conception [relative risk (RR) = 2.4; 95% confidence interval (CI), 1.04–5.7] and higher for children of fathers receiving a total preconceptual ionizing radiation dose of 100 mSv or more (RR = 6.4; 95% CI, 1.57–26.3). hypothesized that irradiation of the testes may be leukomogenic in the offspring. The conclusions of this study have received significant criticism. First, no excess leukemia was noted in the rest of Cumbria where > 90% of the births to Sellafield employees occurred. Second, data on the children of male atomic bomb survivors have not shown an increased incidence of leukemia, despite receiving a significantly greater dose of radiation than the children’s fathers at Sellafield. The results reported by would suggest a much greater genetic sensitivity to radiation and therefore would be less plausible. Third, the results from the study have not been substantiated by other studies that detected no statistically significant excess of leukemia in relation to nuclear facilities in the following locations:
Scotland from 1958 to 1990, including near the Dounreay nuclear installation in Caithness
Ontario, Canada, near five nuclear installations
Southern England, near two sites, and in three areas of northern England
did show a nonstatistically significant increase between childhood leukemia and reported preconceptual exposure of fathers to ionizing radiation [odds ratio (OR) = 2.35; 95% CI, 0.92–6.2]. This study overlapped with another study and the quantity of the exposure to ionizing radiation was not determined.
With regard to diagnostic X rays, ) showed an increased risk for childhood leukemia related to paternal diagnostic x-ray exposure before conception in two separate studies. In the 1994 study, an increased risk was noted if two or more X rays of the lower abdomen were performed (OR = 3.8; 95% CI, 1.5–9.6). No increased risk was noted in the study, however, if the data were restricted to lower abdominal X rays, the more relevant area of exposure.
Mechanisms of potentiation by PPI are discussed in detail elsewhere. Maternal preconception occupational exposure has not been shown to significantly increase the risk for childhood leukemia.
In utero exposure to ionizing radiation
Many studies have attempted to ascertain the effect of in utero radiation exposure and the development of leukemia—particularly related to the atomic bomb exposures in Japan at the end of World War II, the 1986 Chernobyl (Russia) accident, or exposure to diagnostic X rays. An increased risk of childhood leukemia in the offspring of atomic bomb survivors has yet to be shown. Some studies on the Chernobyl accident, which led to widespread radioactive fallout in Europe, have found an increased risk for leukemia in children exposed in utero while living in areas exposed to ionizing radiation after the accident. The observed effects are in question, however, and other studies have not confirmed an increase in risk.
In a critical review of several European studies undertaken 10 years after Chernobyl, overall, no significant association between the risk of childhood leukemia in children 0–14 years of age and exposure from the Chernobyl accident was found. However, a small risk could not be ruled out secondary to limited power and the fact that most studies were descriptive. In a Swedish study, the risk for ALL in children < 5 years of age in highly contaminated areas was increased although not statistically significant (OR = 1.5; 95% CI, 0.8–2.6). Last, in a review of 36 cancer registries in Europe for children 0–14 years of age, the risk for leukemia was increased slightly in the postaccident period, but the overall geographical patterns of change uncovered no relation to the estimated exposure to radiation.
Many studies have assessed the risk of in utero exposure to diagnostic X rays and the development of childhood leukemia, with conflicting results. The potential risk of leukemia in children exposed to diagnostic X rays was first noted in 1956. Many case–control studies have found a consistent association to suggest that radiographic examination of the abdomen of a pregnant woman produces a proportional increase in risk of about 40%. The evidence for causality and for uncertainty is well described. The most notable reason for doubt of a true association is the lack of evidence in cohort studies for an increased risk of leukemia in children exposed to radiation in utero during the atomic bomb blasts in Japan. Furthermore, several recent studies have not found a significant association between childhood leukemia and X-ray examinations in the mother during pregnancy. This apparent decrease in risk over time may be attributable to declining exposures to ionizing radiation (decreased dose) and to the increasing use of diagnostic ultrasound in place of diagnostic X rays during pregnancy.
Postnatal exposure to ionizing radiation
Postnatal exposure to ionizing radiation has been demonstrated to increase the risk of childhood leukemia, most notably from the World War II atomic bomb blasts and radiotherapy for benign disease. Children and adolescents exposed to 1 gray after the bombings were at elevated risk for leukemia (RR = 7.1) and developed leukemia in less time when compared with adults. Several studies have identified an increased risk for childhood leukemia or death due to leukemia secondary to radiotherapy of benign disease whereas others have not (Table 1). This risk appears to be associated with therapeutic radiation for thymus enlargement, ankylosing spondylitis, and ringworm.
Although inconclusive, to date, radiation exposure secondary to the Chernobyl accident has not been shown to increase the risk of leukemia in children who were exposed after birth. Recent studies have shown mixed results regarding exposure to diagnostic X rays during the postnatal period and the risk for childhood leukemia (Table 1). found no significant risk for ALL, even if there were exposure to three or more rays (OR = 1.2; 95% CI, 1.0–1.6). They did note a significant risk for children with pre-B cell ALL, most notably if three or more X rays were performed (OR = 3.2; 95% CI, 1.5–7.2) and if the child was older than 5 years (OR = 3.8; 95% CI, 1.1–13.3). found that exposure to four or more X rays in the postnatal period did not contribute a significant risk to childhood leukemia (OR = 2.3; 95% CI, 0.8–6.5); however, the risk was not evaluated by immunophenotype. Overall, postnatal X-ray studies do not appear to significantly increase the risk of childhood leukemia. Increased risk for specific immunophenotypes may result from certain biases, but this may be an area for further study.
Nonionizing radiation
Numerous epidemiologic studies have been conducted to determine whether an association exists between exposure to nonionizing EMFs and childhood leukemia; some have found a small association while others have not. The inconsistent results of the EMF and childhood leukemia studies may be due in part to differing methods for assessing residential magnetic field exposures and unmeasured EMF characteristics. Furthermore, investigations of animals with exposure to much higher levels of EMFs than humans have not shown increased risk for hematopoietic neoplasia.
conducted a pooled analysis of data collected for nine studies. For the 44 children with leukemia and 62 control children with high estimated residential EMF exposure, the estimated summary relative risk was 2.00 (95% CI, 1.3–3.1). Adjusting for potential confounding variables did not appreciably change the results, but selection bias may have accounted for some of the increase. conducted a case–control study with actual measurements of EMFs in the homes of > 1,200 study subjects near the time of the diagnosis of ALL. Overall, there was no statistically significant increased risk of ALL with increasing exposure to residential magnetic fields (OR = 1.24; 95% CI, 0.86–1.79) for the highest exposure category compared with the lowest. Furthermore, no increased risk of ALL was found based on EMF levels for homes in which the mother resided during pregnancy with the index child. For additional information on nonionizing radiation, see Supplemental Material (http://www.ehponline.org/docs/2006/9023/abstract.html).
Chemicals
The chemical classes most commonly associated with childhood leukemia are hydrocarbons and pesticides. Studies have examined the relationship between childhood leukemia and direct exposure to these chemicals (e.g., use of pesticides in the home) as well as secondary exposure, such as to parents’ clothing worn in an occupational setting where hydrocarbons are used and brought into the home to be laundered.
Hydrocarbons
Hydrocarbons are organic compounds made up primarily of carbon and hydrogen atoms. Examples of hydrocarbon compounds include gasoline and trichloroethylene (spot remover). Hydrocarbons are found in many household and industrial products including paint removers and thinners, and solvents, which are used to dissolve other chemical substances.
The most widely recognized hydrocarbon is benzene, a ubiquitous chemical used in the manufacture of paints and plastics and as a constituent in motor fuels and hobby glues. It is also formed during incomplete combustion of fossil fuels (i.e., petroleum products, coal). Benzene is a known human carcinogen. It has a strong positive exposure–response relationship with leukemia, particularly AML, at a range of exposures not much higher than the current legal standard for workers as recommended by the National Institute for Occupational Safety and Health. A recent occupational study found excess risk for leukemia associated with cumulative benzene exposures and benzene exposure intensities at lower levels (< 60 ppm-years) than had been previously reported (as high as 220 ppm-years). For additional information on benzene, see Supplemental Material (http://www.ehponline.org/docs/2006/9023/abstract.html).
conducted a case-control study of 640 subjects to examine the relationship between parental hobbies and home projects and incidence of childhood leukemia. ALL had a statistically significant association with prenatal exposure to painted homes (> 4 rooms) (OR = 1.7; 95% CI, 1.1–2.7) and to artwork with solvents (OR = 4.1; 95% CI, 1.1–15.1). However, the study was limited by the lack of information about the child’s proximity to the activity and the timeframe of exposure.
In a review by of seven published epidemiologic studies of the association between parental occupation and childhood leukemia, exposure to paints and pigments yielded the most consistently positive results, with several studies producing ORs for ALL and AML of ≥ 1.5. Paternal occupations most associated with increased risk for childhood leukemia in the review included painter, motor vehicle–related worker and machinist or factory worker. In one of the seven epidemiologic studies reviewed, paternal hydrocarbon exposures (e.g., gas station attendant) appeared to be related to both AML and ALL occurring in children ≤ 1 year of age, but this finding could not be confirmed by other studies that covered a broader age range.
In a separate large case–control study, only paternal long-term exposure to plastics during the preconception period showed an increased risk of childhood leukemia, though not statistically significant (OR = 1.4; 95% CI, 1.0–1.9).
There is much speculation about the biological mechanism by which paternal occupational exposures may affect the offspring’s risk for leukemia. Potential mechanisms include genetic alteration of the father’s sperm, which may transmit cancer susceptibility to the child, transplacental fetal exposure after the father brings a toxic exposure into the home, and direct postnatal exposure to chemicals brought home on the clothing (e.g., off-gassing) or indirect exposure through breast-feeding. Exposure through breast milk, however, is an unlikely mechanism as breast-feeding has been associated with a reduced risk of ALL. The reduction in risk was stronger with a longer duration of breast-feeding.
Specific occupations found more frequently among mothers of children with leukemia include metal manufacturing or processing, textiles, and pharmacist. Increased risk for ALL has been described, in a case–control study of more than 3500 children, with maternal occupational exposure to solvents (OR = 1.8; 95% CI, 1.3–2.5) and paints (OR = 1.6; 95% CI, 1.2–2.2) during the preconception period (OR = 1.6; 95% CI, 1.3–2.5), and during pregnancy (OR = 1.7; 95% CI, 1.2–2.3), but not during the postnatal period. Despite these associations, no linear dose–response relationship was observed in this study for any maternal exposure during any time period, and statistically significant associations were found only when maternal occupational exposures were short (equal or below the median).
A recent study in California suggested that children living in areas with high levels of point source carcinogenic hazardous air pollutants (HAPs) are at an increased risk of developing leukemia (RR = 1.3; 95% CI, 1.13–1.6). Selected carcinogenic HAPs included benzene, perchloroethylene, and trichloroethylene. This study had several limitations; most notably the extrapolation of group exposure levels to individuals and exclusion of indoor HAP sources (e.g., tobacco smoke) as potential confounders of exposure estimates.
A recent, similar study in Great Britain reported associations between birthplace of children with leukemia and proximity to industrial sites that release volatile organic compounds, dioxins, 1,3-butadiene, and benzo[a]pyrene.
Pesticides
Many studies have suggested a link between pesticide exposure and childhood leukemia. However, most of these studies are limited by the use of nonspecific pesticide exposure information, small numbers of exposed children, and potential recall bias. Some studies suggest that pesticide-exposed fetuses and children are at higher risks for cancer compared with adults. This suggests that newborns and children may be particularly sensitive to the carcinogenic effects of pesticides. Most children’s exposure to pesticides is from home, lawn, and garden use. Other sources of exposure can include local agricultural applications, contaminated food, parental occupation, and pet products.
In a large meta-analysis of epidemiologic studies that investigated whether occupational or residential exposure to pesticides by either parents or children was related to increased risk of childhood cancer, frequent occupational exposure or in-home pesticide use was associated with childhood leukemia (Table 2). Use of garden pesticides or professional exterminations did not greatly affect risk in this meta-analysis. Some studies have reported increased risk with mothers who had frequent prenatal pesticide exposure in the garden or during pregnancy (OR = 6.5; 95% CI, 1.5–59) and increased risk during childhood with garden insecticides (OR = 2.4; 95% CI, 1.3–4.3) and garden fungicides (OR = 2.5; 95% CI, 1.0–6.2).
Children exposed to professional pest control services at any time 1 year before birth to 3 years after had increased risk as well (OR = 2.8; 95% CI, 1.4–5.7) (Table 2). In a review of 18 studies that assessed the association between pesticide exposure and childhood cancer, no clear patterns of risk by which parent was exposed, by timing of exposure, or by histologic type of leukemia were apparent.
In a recent case–control study conducted in France, for the first time insecticidal shampoo treatment of pediculosis was found to be associated with childhood ALL and AML (OR = 1.9; 95% CI, 1.2–3.3). Various insecticidal shampoos were reported but only the association with pyrethroid-based shampoo was statistically significant (OR = 2.0; 95% CI, 1.1–3.4).
Alcohol, cigarette, and illicit drug use
Studies have shown an increased risk for AML, particularly among very young children, associated with maternal alcohol consumption during pregnancy. examined the effect of alcohol consumption on the risk of developing childhood leukemia, beginning 1 month before and continuing throughout the pregnancy. The risk for AML with maternal alcohol consumption (OR = 2.6; 95% CI, 1.4–5.1) was almost twice that of ALL. Paternal alcohol consumption before conception did not appear to increase risk.
It is unclear whether maternal or paternal cigarette smoking before or during pregnancy is a risk factor for developing childhood leukemia. Two studies found that the frequency, amount, and duration of paternal smoking before conception were related to significantly elevated risk, after adjusting for the effect of maternal smoking., however, found no association between the disease and paternal smoking at any time.
Maternal marijuana use before and during pregnancy has been associated with childhood AML and ALL. Despite a small sample size, findings from a Children’s Cancer Group study showed a 10-fold risk of childhood AML associated with maternal use of marijuana just before or during pregnancy. The authors concluded that, because marijuana has been shown to be a teratogen in animals and possibly humans, it may be leukomogenic, either alone or in combination with a cofactor.
Genetics
Childhood leukemia and other cancers may stem from a combination of genetic susceptibility factors and environmental exposures. The importance of in utero genetic events has been suspected for many years based on concordance studies on twins with leukemia. This is especially true among identical twins. An identical twin is twice as likely as the general population to develop leukemia if his or her twin developed the illness before the age of 7 years. Twins who reach age 15 years without developing leukemia do not appear to be at higher risk of developing the disease.
This concept that some cases of childhood leukemia originate in utero also is the result of genetic studies that have found leukomogenic translocations or clonotypic gene fusion sequences that match that of later leukemic blasts in heelstick blood samples (Guthrie cards) from newborns who later developed ALL. Infant acute leukemia commonly involves gene fusions with the MLL gene. Because (MLL+) acute leukemia can arise after chemotherapy with DNAt2 inhibitors, it is possible that these substances, which are found naturally in certain foods and beverages (e.g., fruits and vegetables, legumes, coffee), may contribute toward infant leukemia.
Studies of archived neonatal blood spots in which a specific gene fusion occurs [t(1;19)/E2A-PBX1] support the theory that not all cases of childhood ALL develop in utero. The association of leukemogenesis in children with metabolizing gene variants suggests a causal relationship to environmental exposures that may occur during the postnatal period. Increased risk of childhood leukemia has recently been associated with genetic polymorphisms that disrupt the hosts’ abilities to properly metabolize and transport xenobiotic exposures. Furthermore, polymorphic genes encoding carcinogen- and drug-metabolizing enzymes may not only increase the risk of ALL but also influence the risk of relapse in patients and therefore help to predict disease outcome. For example, the prognosis of patients with cytochrome P450 1A1 (CYP1A1) and NAD(P)H quinine oxi-doreductase 1 (NQO1) variants has been found to be worse than that of patients who lack these variants.
Although genetic syndromes account for only a small proportion of childhood leukemias, certain inherited diseases are associated with a higher risk of developing leukemia. Examples of these diseases include Fanconi anemia, Bloom syndrome, ataxia telangiectasia, Down syndrome, Shwachman syndrome, and neurofibromatosis. These inherited diseases are characterized by defective DNA repair, chromosome aneuploidy (an abnormal number of chromosomes), or chromosomal abnormalities such as translocations. AML has a higher incidence during the neonatal period than ALL among children with Fanconi anemia, Bloom syndrome, and Down syndrome.
Siblings of children with leukemia are at greater risk of developing leukemia than children whose siblings do not have the disease. Also, a positive family history of hematopoietic malignancies among first- or second-degree relatives has been associated with a small increased risk for childhood ALL. Furthermore, the risk for ALL is not increased in children with a family history of cancers other than hematopoietic malignancies.
Infectious Agents and the Population Mixing Theory
Several observations contribute to the theory that a transmissible agent is potentially involved in the oncogenic process of childhood leukemia. First, the peak incidence of childhood leukemia and that of common childhood infections both occur among children 2–5 years of age, the age group least likely to possess sophisticated immune systems. Second, a viral etiology has been shown for some animal and human cancers (e.g., Epstein-Barr virus for Burkitt lymphoma). Third, evidence exists of an apparent seasonal variation in the birth or onset dates of childhood leukemia. Statistically significant seasonal variation for ALL with a peak in the summer, in the autumn–winter and in the early spring among 1- to 6-year-old children have been described. However, a large study of > 15,000 cases of childhood leukemia born and diagnosed in the United Kingdom found no evidence of seasonality in either month of birth or month of diagnosis in any subgroup of childhood cancer. Last, an excess of childhood leukemia has been found in rural, potentially immunologically naïve, populations that have undergone an influx of permanent residents; this theory is known as population mixing. suggested that an extremely infectious but not highly pathogenic agent introduced into a previously unexposed community might cause an epidemic of ALL. Susceptible individuals who live in rural areas in which the population suddenly increases, or for which the composition changes regularly, may be exposed to infectious agents that are brought into the area by new residents, possibly triggering a cluster of cases of ALL. The theory implies that the differences in rates of leukemia in rural areas are due to differences in herd, or population, immunity. Results from other studies support this theory. For additional information on population mixing, see Supplemental Material (http://www.ehponline.org/docs/2006/9023/abstract.html).
An alternative hypothesis to Kinlen’s suggests that the mechanism of “delayed infection” is responsible, and that an abnormal response to the infection promotes a second event critical for the development of ALL. Support of this hypothesis comes from studies showing that children with ALL are less likely to have had common infections, perhaps as a result of immunologic isolation early in life. Proposed mechanisms for an abnormal response to an as yet unidentified infectious agent might include leukemogenicity of the virus itself, which may directly infect and transform B-precursor cells, or physical characteristics of the virus that stimulate critical receptors for cell growth.
Maternal reproductive history and birth characteristics
Conflicting results have been reported from studies of the relationship between maternal history of fetal loss and risk for ALL or AML. A history of fetal loss may reflect genetic predisposition, abnormal intrauterine environment, or the effect of a common environmental exposure.
The risk for childhood ALL has been shown to be significantly higher among children who were born when their parents were older; significant trends in ALL incidence have been related to increasing mother’s (> 35 years, p < 0.001) and father’s (> 40 years, p < 0.002) ages. For children born to mothers and fathers ≥ 40 years of age, the odds ratio for offspring developing childhood leukemia was 1.97 and 1.45, respectively.
Several studies have described an association between increased birth weight and childhood ALL, particularly ALL developing early in life. Increased birth weight has been associated with a high rate of cell proliferation and with an increase in the number of precursor cells that are at risk for malignant transformation. However, birth weight tends to increase with maternal age, which is also a known risk factor for ALL in offspring.
For information on medications/therapeutic agents, military history and nutrition in relation to childhood leukemia, see Supplemental Material (http://www.ehponline.org/docs/2006/9023/abstract.html).
Conclusion
ALL and AML are the most common malignancies of childhood. Despite many advances in the treatment of childhood leukemia, the causative factors of ALL and AML remain unclear. Identifying risk factors for childhood leukemia (e.g., environmental, genetic, infectious) is an important step in the reduction of the overall burden of the disease. In general, benzene and ionizing radiation are two environmental exposures strongly associated with the development of childhood AML or ALL. However, identifying other environmental risk factors associated with leukemia is difficult for several reasons:
inability to confirm and quantify exposures;
lack of a prospective cohort;
presence of different variants of leukemia; presence of confounders; and
inadequate understanding of the pathophysiology of leukemia (e.g., gene–environment or infection–environment interaction).
Future attempts to overcome these obstacles (e.g., through improving laboratory detection methods to confirm exposure; prospective cohort studies; focusing on specific types of leukemia and specific chemical agents) could possibly uncover other environmental risk factors associated with childhood leukemia and mitigate potentially harmful exposures to reduce the risk for disease. Future studies, when appropriate, should attempt to use common questionnaires, address timing and route of exposure, document evidence that exposure has actually been transferred from the workplace to the child, and store biological samples when possible.
Correction
In the Abstract and in the section “Risk Factors,” the sentences “Only two environmental risk factors (benzene and ionizing radiation) have been significantly linked to ALL or AML” in the original manuscript published online have been changed here to “Only one environmental risk factor (ionizing radiation) has been significantly linked to ALL or AML.”
References 145
- 1.
- 2.
Alexander FE, Chan LC, Lam TH, Yuen P, Leung NK, Ha SY, et al. Clustering of childhood leukaemia in Hong Kong: association with the childhood peak and common acute lymphoblastic leukaemia and with population mixing. Br J Cancer. 1997;75:457-463.
Not in our library10.1038/bjc.1997.77
- 3.
Alexander FE, Patheal SL, Biondi A, Brandalise S, Cabrera ME, Chan LC, et al. Transplacental chemical exposure and risk of infant leukemia with MLL gene fusion. Cancer Research. 2001;61:2542-2546.
Not in our library
- 4.
Bhatia S. Influence of race and socioeconomic status on outcome of children treated for childhood acute lymphoblastic leukemia. Curr Opin Pediatr. 2004;16:9-14.
Not in our library10.1097/00008480-200402000-00004
- 5.
Bleyer A, Sposto R, Sather H. In the United States, pediatric brain tumors and other nervous system tumors are now more common than childhood acute lymphoblastic leukemia (ALL) and have a 3-fold greater national mortality rate than ALL [Abstract]. Proc Am Soc Clin Oncol. 1998;17:389a.
Not in our library
- 6.
Boice J. Cancer following irradiation in childhood and adolescence. Med Pediatr Onc (suppl). 1996;1:29-34.
Not in our library
- 7.
Boice J, Miller R. Childhood and adult cancer after intrauterine exposure to ionizing radiation. Teratology. 1999;59:227-233.
Not in our library10.1002/(sici)1096-9926(199904)59:4<227::aid-tera7>3.0.co;2-e
- 8.
Boutou O, Guizard A-V, Slama R, Pottier D, Spira A. Population mixing and leukaemia in young people around the La Hague nuclear waste reprocessing plant. Br J Cancer. 2002;87:740-745.
Not in our library10.1038/sj.bjc.6600529
- 9.
Bowman JD, Thomas DC. Re: “Are children living near high-voltage power lines at increased risk of acute lymphoblastic leukemia? Am J Epidemiol. 2001;153:615-617.
Not in our library10.1093/aje/153.6.615-a
- 10.
Brain JD, Kavet R, McCormick DL, Poole C, Silverman LB, Smith TJ, et al. Childhood leukemia: electric and magnetic fields (EMF) as possible risk factors. Environ Health Perspect. 2003;111:962-970.
Not in our library10.1289/ehp.6020
- 11.
Brondum J, Shu XO, Steinbuch M, Severson RK, Potter JD, Robison LL. Parental cigarette smoking and the risk of acute leukemia in children. Cancer. 1999;85:1380-1388.
Not in our library
- 12.
Buckley JD, Robison LL, Swotinsky R, Garabrant DH, LeBeau M, Manchester P, et al. Occupational exposures of parents of children with acute nonlymphoblastic leukemia: a report from the Children’s Cancer Study Group. Cancer Res. 1989;49:4030-4037.
Not in our library
- 13.
Canalle R, Burim RV, Tone LG, Takahashi CS. Genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia. Environ Mol Mutagen. 2004;43:100-109.
Not in our library10.1002/em.20003
- 14.
Clarkson B, Boyse EA. Possible explanation of high concordance for acute leukemia in monozygous twins. Lancet. 1971;1:699-701.
Not in our library10.1016/s0140-6736(71)92705-x
- 15.
Daniels JL, Olshan AF, Savitz DA. Pesticides and childhood cancers. Environ Health Perspect. 1997;105:1068-1077.
Not in our library10.1289/ehp.971051068
- 16.
- 17.
Davies A, Modan B, Djaldetti M, deVries A. Epidemiological observations on leukemia in Israel. Arch Intern Med. 1961;108:86-90.
Not in our library10.1001/archinte.1961.03620070088011
- 18.
Dockerty JD, Draper G, Vincent T, Rowan SD, Bunch KJ. Case-control study of parental age, parity and socioeconomic level in relationship to childhood cancers. Int J Epidemiol. 2001;30:1428-1437.
Not in our library10.1093/ije/30.6.1428
- 19.
Doll R, Evans HJ, Darby SC. Paternal exposure not to blame. Nature. 1994;367:678-680.
Not in our library10.1038/367678a0
- 20.
Doll R, Wakeford R. Risk of childhood cancer from fetal irradiation. Br J Radiol. 1997;70:130-139.
Not in our library10.1259/bjr.70.830.9135438
- 21.
Dordelmann M, Schrappe M, Reter A, Zimmerman M, Graf N, Schott G, et al. Down’s syndrome in childhood acute lymphoblastic leukemia: clinical characteristics and and treatment outcome in four consecutive BFM trials, Berlin-Frankfurt-Munster Group. Leukemia. 1998;12:645-651.
Not in our library10.1038/sj.leu.2400989
- 22.
Draper GJ, Heaf MM, Kinnier Wilson LM. Occurrence of childhood cancers among sibs and estimation of familial risks. J Med Genet. 1977;14:81-90.
Not in our library10.1136/jmg.14.2.81
- 23.
Draper GJ, Stiller CA, Cartwright RA, Craft AW, Vincent TJ. Cancer in Cumbria and in the vicinity of the Sellafield nuclear installation, 1963–1990. BMJ. 1993;306:89-94.
Not in our library10.1136/bmj.306.6870.89
- 24.
Feltbower RG, Pearce MS, Dickinson HO, Parker L, McKinney PA. Seasonality of birth for cancer in Northern England, UK. Paediatr Perinat Epidemiol. 2001;15:338-345.
Not in our library10.1046/j.1365-3016.2001.00377.x
- 25.
Freedman MD, Stewart P, Kleinerman RA, Wacholder S, Hatch EE, Tarone RE, et al. Household solvent exposures and childhood acute lymphoblastic leukemia. Am J Public Health. 2001;91:564-567.
Not in our library10.2105/ajph.91.4.564
- 26.
Gale KB, Ford AM, Repp R, Borkhardt A, Keller C, Eden OB, et al. Backtracking leukemia to birth: identification of clonotypic gene fusion sequences in neonatal blood spots. Proc Natl Acad Sci USA. 1997;94:13950-13954.
Not in our library10.1073/pnas.94.25.13950
- 27.
Gardner MJ. Father’s occupational exposure to radiation and the raised level of childhood leukemia near the Sellafield Nuclear Plant. Environ Health Perspect. 1991;94:5-7.
Not in our library10.1289/ehp.94-1567974
- 28.
Gardner MJ, Snee MP, Hall AJ, Powell CA, Downes S, Terrell JD. Results of case-control study of leukemia and lymphoma among young people near Sellafield nuclear plant in West Cumbria. BMJ. 1990;300:423-429.
Not in our library10.1136/bmj.300.6722.423
- 29.
Gilman EA, Knox EG. Geographical distribution of birth places of children with cancer in the UK. Br J Cancer. 1998;77:842-849.
Not in our library10.1038/bjc.1998.137
- 30.
Glass DC. Leukemia risk associated with low-level benzene exposure. Epidemiology. 2003;14:569-577.
Not in our library10.1097/01.ede.0000082001.05563.e0
- 31.
Greaves MF. Childhood leukemia. BMJ. 2002;324:283-287.
Not in our library10.1136/bmj.324.7332.283
- 32.
Greaves MF, Alexander FE. An infectious etiology for common acute lymphoblastic leukemia in childhood? Leukemia. 1993;7(3):349-360.
Not in our library
- 33.
Greaves MF, Maia AT, Wiemels JL, Ford AM. Leukemia in twins: lessons in natural history. Blood. 2003;102:2321-2333.
Not in our library10.1182/blood-2002-12-3817
- 34.
Greenland S, Sheppard AR, Kaune WT, Poole C, Kelsh MA. A pooled analysis of magnetic fields, wire codes, and childhood leukemia, Childhood-EMF Study Group. Epidemiology. 2000;11:624-634.
Not in our library10.1097/00001648-200011000-00003
- 35.
Greenlee RT, Murray T, Bolden S, Wingo PA. Cancer statistics 2000. CA Cancer J Clin. 2000;50:7-34.
Not in our library10.3322/canjclin.50.1.7
- 36.
Gross L. Viral etiology of cancer and leukemia: a look into the past, present and future. Cancer Res. 1978;38:485-493.
Not in our library
- 37.
Grossman J. What’s hiding under the sink: dangers of household pesticides. Environ Health Perspect. 1995;103:550-554.
Not in our library10.1289/ehp.95103550
- 38.
Gurney JG, Severson RK, Davis S, Robison LL. Incidence of cancer in children in the United States, sex, race, and 1-year age-specific rates by histologic type. Cancer. 1995;75:2186-2195.
Not in our library10.1002/1097-0142(19950415)75:8<2186::aid-cncr2820750825>3.0.co;2-f
- 39.
Hardell L, Holmberg B, Malker H, Paulsson LE. Exposure to extremely low frequency electromagnetic fields and the risk of malignant disease—an evaluation of epidemiological and experimental findings. Eur J Cancer Prev. 1995;4(suppl 1):3-107.
Not in our library10.1097/00008469-199509001-00001
- 40.
Hatch EE, Linet MS, Kleinerman RA, Tarone RE, Severson RK, Hartsock CT, et al. Association between childhood acute lymphoblastic leukemia and use of electrical appliances during pregnancy and childhood. Epidemiology. 1998;9:234-245.
Not in our library
- 41.
Heath CW, Moloney WC. Familial leukemia: five cases of acute leukemia in three generations. N Engl J Med. 1965;272:882-887.
Not in our library10.1056/nejm196504292721703
- 42.
Higgins CD, dos-Santos-Silva I, Stiller CA, Swerdlow AJ. Season of birth and diagnosis of children with leukaemia: an analysis of over 15000 UK cases occurring from 1953–95. Br J Cancer. 2001;84:406-412.
Not in our library10.1054/bjoc.2000.1575
- 43.
Hjalmars U, Kulldorff M, Gustafsson G. Risk of acute childhood leukemia in Sweden after the Chernobyl reactor accident. BMJ. 1994;309:154-157.
Not in our library10.1136/bmj.309.6948.154
- 44.
Infante-Rivard C, Guiguet M. Family history of hematopoietic and other cancers in children with acute lymphoblastic leukemia. Cancer Detect Prev. 2004;28:83-87.
Not in our library10.1016/j.cdp.2003.12.003
- 45.
Infante-Rivard C, Jacques L. Empirical study of parental recall bias. Am J Epidemiol. 2000;152:480-486.
Not in our library10.1093/aje/152.5.480
- 46.
Infante-Rivard C, Labuda D, Krajinovic M, Sinnett D. Risk of childhood leukemia associated with exposure to pesticides and with gene polymorphisms. Epidemiology. 1999;10:481-487.
Not in our library
- 47.
Ji BT, Shu XO, Linet M, Xheng W, Wacholder S, Gao YT, et al. Paternal cigarette smoking and risk for childhood cancer among offspring of nonsmoking mothers. J Natl Cancer Inst. 1997;89:238-244.
Not in our library10.1093/jnci/89.3.238
- 48.
Kalwinsky DK, Rivera G, Dahl GV, Roberson P, George S, Murphy SB, et al. Variation by race in presenting clinical and biologic features of childhood acute lymphoblastic leukemia: implications for treatment outcome. Leuk Res. 1985;9:817-823.
Not in our library10.1016/0145-2126(85)90300-5
- 49.
Karimi M, Yarmohammadi H. Seasonal variations in the onset of childhood leukemia/lymphoma: April 1996 to March 2000, Shiraz, Iran. Hematol Oncol. 2003;21:51-55.
Not in our library10.1002/hon.702
- 50.
Kaye SA, Robison LL, Smithson WA, Gunderson P, King FL, Neglia JP. Maternal reproductive history and birth characteristics in childhood acute lymphoblastic leukemia. Cancer. 1991;68:1351-1355.
Not in our library10.1002/1097-0142(19910915)68:6<1351::aid-cncr2820680627>3.0.co;2-j
- 51.
Kersey JH, Sabad A, Gajl-Peczalska K, Hallgren HM, Yunis EJ, Nesbit ME. Acute lymphoblastic leukemia cells with T (thymus-derived) lymphocyte markers. Science. 1973;183:1355-1356.
Not in our library10.1126/science.182.4119.1355
- 52.
Kinlen LJ. Evidence for an infective cause of childhood leukaemia: comparison of a Scottish new town with nuclear reprocessing sites in Britain. Lancet. 1988;322(8624):1323-1327.
Not in our library10.1016/s0140-6736(88)90867-7
- 53.
- 54.
Kinlen LJ, Clarke K, Balkwill A. Paternal preconceptional radiation exposure in the nuclear industry and leukaemia and non-Hodgkin’s lymphoma in young people in Scotland. BMJ. 1993;306:1153-1158.
Not in our library10.1136/bmj.306.6886.1153
- 55.
Kinlen LJ, Hudson C, Stiller LA. Contacts between adults as evidence for an infective origin of childhood leukemia: an explanation for the excess near nuclear establishments in West Berkshire? Br J Cancer. 1991;64:549-554.
Not in our library10.1038/bjc.1991.348
- 56.
Kleinerman RA, Kaune WT, Hatch EE, Wacholder S, Linet MS, Robison LL, et al. Are children living near high-voltage power lines at increased risk of acute lymphoblastic leukemia? Am J Epidemiol. 2000;151:512-515.
Not in our library10.1093/oxfordjournals.aje.a010237
- 57.
Knox EG. Childhood cancers and atmospheric carcinogens. J Epidemiol Community Health. 2005;59:101-105.
Not in our library10.1136/jech.2004.021675
- 58.
Koushik A, King WD, McLaughlin JR. An ecologic study of childhood and population mixing in Ontario, Canada. Cancer Causes Control. 2001;12:483-490.
Not in our library10.1023/a:1011266413087
- 59.
Krajinovic M, Labuda D, Sinnett D. Childhood acute lymphoblastic leukemia: genetic determinants of susceptibility and disease outcome. Rev Environ Health. 2001;16:263-279.
Not in our library10.1515/reveh.2001.16.4.263
- 60.
Krajinovic M, Labuda D, Sinnett D. Glutathione S-trans-ferase P1 genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukaemia. Pharmacogenetics. 2002;12:655-658.
Not in our library10.1097/00008571-200211000-00010
- 61.
Leiss JK, Savitz DA. Home pesticide use and childhood cancer: a case-control study. Am J Public Health. 1995;85:249-252.
Not in our library10.2105/ajph.85.2.249
- 62.
Linet MS, Hatch EE, Kleinerman RA, Robison LL, Kaune WT, Friedman DR, et al. Residential exposure to magnetic fields and acute lymphoblastic leukemia in children. N Engl J Med. 1997;337:1-7.
Not in our library10.1056/nejm199707033370101
- 63.
Linet MS, Ries LA, Smith MA, Tarone RE, Devesa SS. Cancer surveillance series: recent trends in childhood cancer incidence and mortality in the United States. J Natl Cancer Inst. 1999;91:1051-1058.
Not in our library10.1093/jnci/91.12.1051
- 64.
Little MP. A comparison between the risk of childhood leukemia from parental exposure to radiation in the Sellafield work force and those displayed among the Japanese atomic bomb survivors. J Radiol Protection. 1990;10:185-198.
Not in our library
- 65.
Lord BI. Transgenerational susceptibility to leukemia induction resulting from preconception, paternal irradiation. Int J Radiat Biol. 1999;75:801-810.
Not in our library10.1080/095530099139854
- 66.
Lowengart RA. Childhood leukemia and parent’s occupational and home exposures. J Natl Cancer Inst. 1987;79:39-46.
Not in our library
- 67.
Lundell M, Holm LE. Mortality from leukemia after irradiation in infancy for skin hemangioma. Radiat Res. 1996;145:595-601.
Not in our library
- 68.
- 69.
Mahoney MC, Moysich KB, McCarthy PL, McDonald RC, Stepanenko VF, Day RW, et al. The Chernobyl childhood leukemia study: background & lessons learned. Environ Health. 2004;3(1):12.
Not in our library10.1186/1476-069x-3-12
- 70.
Margolin JF Steuber CP Poplack DG 2001. Acute lymphocytic leukemia. In: Principles and Practice of Pediatric Oncology (Pizzo PA, Poplack DG, eds). Philadelphia:JB Lippincott, 489–544.
Not in our library
- 71.
McKinney PA, Alexander FE, Cartwright RA, Parker L. Parental occupations of children with leukemia in west Cumbria, north Humberside, and Gateshead. BMJ. 1991;302:681-687.
Not in our library10.1136/bmj.302.6778.681
- 72.
McLaughlin JR, King WD, Anderson TW, Clarke EA, Ashmore JP. Paternal radiation exposure and leukaemia in offspring: the Ontario case-control study. BMJ. 1993;307:959-966.
Not in our library10.1136/bmj.307.6910.959
- 73.
Meinert R, Kaletsch U, Kaatsch P, Schuz J, Michaelis J. Associations between childhood cancer and ionizing radiation: Results of a population-based case-control study in Germany. Cancer Epidemiol Biomarkers Prev. 1999;8:793-799.
Not in our library
- 74.
Menegaux F, Baruchel A, Bertrand Y, Lescoeur B, Leverger G, Nelken B, et al. Household exposure to pesticides and risk of childhood acute leukaemia. Occup Environ Med. 2006;63:131-134.
Not in our library10.1136/oem.2005.023036
- 75.
Michaelis J, Kaletsch U, Burkart W, Grosche B. Infant leukaemia after the Chernobyl accident [Letter]. Nature. 1997;387:246.
Not in our library10.1038/387246a0
- 76.
Miller RW. Persons with exceptionally high risk of leukemia. Cancer Res. 1967;27:2420-2423.
Not in our library
- 77.
Miller RW. Relationship between cancer and congenital defects: an epidemiologic evaluation. J Natl Cancer Inst. 1968;40(5):1079-1085.
Not in our library
- 78.
Moloney W. Leukemia in survivors of atomic bombing. N Engl J Med. 1955;253:88-90.
Not in our library10.1056/nejm195507212530302
- 79.
Moysich KB, Menezes RJ, Michalek AM. Chernobyl-related ionising radiation exposure and cancer risk: an epidemiological review. Lancet Oncol. 2002;3:269-279.
Not in our library10.1016/s1470-2045(02)00727-1
- 80.
Murray R, Heckel P, Hempelmann L. Leukemia in children exposed to ionizing radiation. N Engl J Med. 1959;261:585-589.
Not in our library10.1056/nejm195909172611203
- 81.
Myers A, Cllyden A, Cartwright RA, Cartwright SC. Childhood cancer and overhead powerlines: a case-control study. Br J Cancer. 1990;62:1008-1014.
Not in our library10.1038/bjc.1990.428
- 82.
This reference’s wording can’t be shown under the paper’s licence.
Not in our library
- 83.
Naumberg E, Bellocco R, Cnattingius S, Hall P, Boice JD, Ekbom A. Intrauterine exposure to diagnostic x-rays and risk of childhood leukemia subtypes. Radiat Res. 2001;156:718-723.
Not in our library10.1667/0033-7587(2001)156[0718:ietdxr]2.0.co;2
- 84.
Neel JV, Schull WJ.
Not in our library
- 85.
Noshchenko AG, Moysich KB, Bondar A. Patterns of acute leukemia occurrence among children in the Chernobyl region. Int J Epidemiol. 2001;30:125-129.
Not in our library10.1093/ije/30.1.125
- 86.
Parkin DM, Cardis E, Masuyer E, Friedl HP, Hansluwka H, Bobev D, et al. Childhood leukemia following the Chernobyl accident: the European Childhood Leukemia-Lymphoma Incidence Study (ECLIS). Eur J Cancer. 1993;29a:87-95.
Not in our library10.1016/0959-8049(93)90582-z
- 87.
Parkin DM, Clayton D, Black RJ, Masuyer E, Friedl HP, Ivanov E, et al. Childhood leukaemia in Europe after Chernobyl: 5 year follow-up. Br J Cancer. 1996;73:1006-1012.
Not in our library10.1038/bjc.1996.197
- 88.
Petridou E, Trichopoulos D, Dessypris N, Flytzani V, Haidas S, Kalmanti M, et al. Infant leukemia after in utero exposure to radiation from Chernobyl. Nature. 1996;382:303-304.
Not in our library10.1038/382352a0
- 89.
Pierce M. Childhood leukemia. J Pediatr. 1936;8:66-95.
Not in our library
- 90.
Pinkel D. Ethnicity and survival in children acute lymphoid leukemia. Leukemia. 1993;7(suppl 2):S146-S147.
Not in our library
- 91.
Pollock BH, DeBaun MR, Camitta BM, Shuster JJ, Ravindranath Y, Pullen DJ, et al. Racial differences in the survival of childhood B-precursor acute lymphoblastic leukemia: a Pediatric Oncology Group study. J Clin Oncol. 2000;18:813-823.
Not in our library10.1200/jco.2000.18.4.813
- 92.
Pui CH. Acute lymphocytic leukemia. Pediatr Clin North Am. 1997;44(4):831-846.
Not in our library10.1016/s0031-3955(05)70532-0
- 93.
Pui CH. Acute lymphocytic leukemia in children. Curr Opin Oncol. 2000;12:3-12.
Not in our library10.1097/00001622-200001000-00002
- 94.
Pui CH, Sandlund JT, Pei D, Rivera GK, Howard SC, Ribeiro RC, et al. Results of therapy for acute lymphoblastic leukemia in black and white children. JAMA. 2003;290:2001-2007.
Not in our library10.1001/jama.290.15.2001
- 95.
Reynolds P, Behren JV, Gunier RB, Goldberg DE, Hertz A, Harnly ME. Childhood cancer and agricultural pesticide use: an ecologic study in California. Environ Health Perspect. 2002;110:319-324.
Not in our library10.1289/ehp.02110319
- 96.
Reynolds P, Behren JV, Gunier RB, Goldberg DE, Hertz A, Smith DF. Childhood cancer incidence rates and hazardous air pollutants in California: an exploratory analysis. Environ Health Perspect. 2003;111:663-668.
Not in our library10.1289/ehp.5986
- 97.
Ries LAG, Kosary CL, Hankey BF, Miller BA, Clegg L, Mariotto A, et al.
Not in our library
- 98.
Rinsky RA. Leukemia in benzene workers. Am J Ind Med. 1981;2:217-245.
Not in our library10.1002/ajim.4700020305
- 99.
Rivard CE, Deadman JE. Maternal occupational exposure to extremely low frequency magnetic fields during pregnancy and childhood leukemia. Epidemiology. 2003;14:437-441.
Not in our library10.1097/01.ede.0000078421.60231.bc
- 100.
Robison LL, Buckley JD, Daigle AE, Wells R, Benjamin D, Arthur DC, et al. Maternal drug use and risk of childhood non-lymphoblastic leukemia among offspring: an epidemiologic investigation implicating marijuana (a report from the Children’s Cancer Study Group). Cancer. 1989;63:1904-1911.
Not in our library
- 101.
Robison LL, Codd M, Gunderson P, Neglia JP, Smithson WA, King FL. Birth weight as a risk factor for childhood acute lymphoblastic leukemia. Pediatr Hematol Oncol. 1987;4:63-72.
Not in our library10.3109/08880018709141250
- 102.
Robison LL, Neglia JP. Epidemiology of Down syndrome and childhood acute leukemia. Prog Clin Biol Res. 1987;246:19-32.
Not in our library
- 103.
Roman E, Watson A, Beral V, Buckle S, Bull D, Baker K, et al. Case-control study of leukemia and non-Hodgkin’s lymphoma among children aged 0–4 years living in west Berkshire and north Hampshire health districts. BMJ. 1993;306:615-621.
Not in our library10.1136/bmj.306.6878.615
- 104.
Ron E. Ionizing radiation and cancer risk: evidence from epidemiology. Radiat Res. 1998;150:S30-S41.
Not in our library
- 105.
Ron E, Modan B, Boice JD. Mortality after radiotherapy for ringworm of the scalp. Am J Epidemiol. 1988;127:713-725.
Not in our library10.1093/oxfordjournals.aje.a114852
- 106.
Ross JA, Davies SM, Potter JD, Robison LL. Epidemiology of childhood leukemia with a focus on infants. Epidemiol Rev. 1994;16:243-272.
Not in our library10.1093/oxfordjournals.epirev.a036153
- 107.
Ross JA, Potter JD, Reaman GH, Pendergrass TW, Robison LL. Maternal exposure to potential inhibitors of DNA topoisomerase II and infant leukemia (United States): a report from the Children’s Cancer Group. Cancer Causes Control. 1996;7:581-590.
Not in our library10.1007/bf00051700
- 108.
Ross JA, Potter JD, Shu XO, Reaman GH, Lampkin B, Robison LL. Evaluating the relationship among maternal reproductive history, birth characteristics, and infant leukemia: a report from the Children’s Cancer Group. Ann Epidemiol. 1997;7:172-179.
Not in our library10.1016/s1047-2797(97)00012-4
- 109.
Ross JA, Severson RK, Swensen AR, Pollock BH, Gurney JG, Robison LL. Seasonal variation in the diagnosis of childhood cancer in the United States. Br J Cancer. 1999;81:549-553.
Not in our library10.1038/sj.bjc.6690729
- 110.
Rushton L, Romaniuk H. A case-control study to investigate the risk of leukemia associated with exposure to benzene in petroleum marketing and distribution workers in the United Kingdom. Occup Environ Med. 1997;54:152-166.
Not in our library10.1136/oem.54.3.152
- 111.
Sali D, Cardis E, Sztanyik L, Auvinen A, Bairakova A, Dontas N, et al. Cancer consequences of the Chernobyl accident in Europe outside the former USSR: a review. Int J Cancer. 1996;67:343-352.
Not in our library10.1002/(sici)1097-0215(19960729)67:3<343::aid-ijc7>3.0.co;2-r
- 112.
Sandler DP, Ross JA. Epidemiology of acute leukemia in children and adults. Semin Oncol. 1997;24:3-16.
Not in our library
- 113.
Savitz DA, Chen J. Parental occupation and childhood cancer: review of epidemiologic studies. Environ Health Perspect. 1990;88:325-337.
Not in our library10.1289/ehp.9088325
- 114.
Schnatter RA, Armstrong TW, Nicolich MJ, Thompson FS, Katz AM, Huebner WW, et al. Lymphohaematopoietic malignancies and quantitative estimates of exposure to benzene in Canadian petroleum distribution workers. Occup Environ Med. 1996;53:773-781.
Not in our library10.1136/oem.53.11.773
- 115.
Schulz KF, Grimes DA. Case-control studies: research in reverse. Lancet. 2002;359:431-434.
Not in our library10.1016/s0140-6736(02)07605-5
- 116.
Shearer P, Parham D, Kovnar E, Kun L, Rao B, Lobe T, et al. Neurofibromatosis type I and malignancy: review of 32 pediatric cases treated at a single institution. Med Pediatr Oncol. 1994;22:78-83.
Not in our library10.1002/mpo.2950220203
- 117.
Shu XO, Linet MS, Steinbuch M, Wen WQ, Buckley JD, Neglia JP, et al. Breast feeding and risk of acute childhood leukemia. J Natl Cancer Inst. 1999a;91(20):1765-1772.
Not in our library10.1093/jnci/91.20.1765
- 118.
Shu XO, Potter JD, Linet MS, Severson RK, Han D, Kersey JH, et al. Diagnostic x-rays and ultrasound exposure and risk of acute lymphoblastic leukemia by immunophenotype. Cancer Epidemiol Biomarkers Prev. 2002;11:177-185.
Not in our library
- 119.
Shu XO, Reaman GH, Lampkin B, Sather HN, Pendergrass TW, Robison LL. Association of paternal diagnostic X-ray exposure with risk of infant leukemia. Cancer Epidemiol Biomarkers Prev. 1994;3:645-653.
Not in our library
- 120.
Shu XO, Ross JA, Pendergrass TW, Reaman GH, Lampkin B, Robison LL. Parental alcohol consumption, cigarette smoking, and risk of infant leukemia: a Children’s Cancer Group study. J Natl Cancer Inst. 1996;88(1):24-31.
Not in our library10.1093/jnci/88.1.24
- 121.
Shu XO, Stewart P, Wen WQ, Han D, Potter JD, Buckley JD, et al. Parental occupational exposure to hydrocarbons and risk of acute lymphocytic leukemia in offspring. Cancer Epidemiol Biomarkers Prev. 1999b;8:783-791.
Not in our library
- 122.
Sorahan T, Lancashire R, Prior P, Stewart A. Childhood cancer and parental use of alcohol and tobacco. Ann Epidemiol. 1995;5:354-359.
Not in our library10.1016/1047-2797(95)00032-3
- 123.
Spector LG, Xie Y, Robison LL, Heerema NA, Hilden JM, Lange B, et al. Maternal diet and infant leukemia: the DNA topoisomerase II inhibitor hypothesis: a report from the children’s oncology group. Cancer Epidemiol Biomarkers Prev. 2005;14:651-655.
Not in our library10.1158/1055-9965.epi-04-0602
- 124.
Steiner M, Burkart W, Grosche B, Kaletsch U, Michaelis J. Trends in infant leukemia in West Germany in relationship to in utero exposure due to Chernobyl accident. Radiat Environ Biophys. 1998;37:87-93.
Not in our library10.1007/s004110050099
- 125.
Stewart A, Webb K, Giles D. Malignant disease in childhood and diagnostic irradiation in utero [Letter]. Lancet. 1956;2:447.
Not in our library10.1016/s0140-6736(56)91923-7
- 126.
Swensen AR, Ross JA, Severson RK, Pollock BH, Robison LL. The age peak in childhood acute lymphoblastic leukemia: exploring the potential relationship with socioeconomic status. Cancer. 1997;79(10):2045-2051.
Not in our library10.1002/(sici)1097-0142(19970515)79:10<2045::aid-cncr28>3.0.co;2-t
- 127.
Swift M. Fanconi’s anemia in the genetics of neoplasia. Nature. 1971;230:370-373.
Not in our library10.1038/230370a0
- 128.
Toledano S, Lange B. Ataxia-telangiectasia and acute lymphoblastic leukemia. Cancer. 1980;45:1675-1678.
Not in our library10.1002/1097-0142(19800401)45:7<1675::aid-cncr2820450725>3.0.co;2-d
- 129.
This reference’s wording can’t be shown under the paper’s licence.
Not in our library
- 130.
Urquhart JD, Black RJ, Muirhead MJ, Sharp L, Maxwell M, Eden OB, et al. Case-control study of leukaemia and non-Hodgkin’s lymphoma in children in Caithness near the Dounreay nuclear installation. BMJ. 1991;302:687-692.
Not in our library10.1136/bmj.302.6778.687
- 131.
Van Duijn CM, Van Steensel-Moll HA, Coebergh JW, Van Zanen GE. Risk factors for childhood acute non-lymphocytic leukemia: an association with maternal alcohol consumption during pregnancy? Cancer Epidemiol Biomarkers Prevent. 1994;3:457-460.
Not in our library
- 132.
Van Steensel-Moll HA, Valkenbueg HA, Van Zanen GE. Childhood leukemia and parental occupation, a register-based case-control study. Am J Epidemiol. 1985;121:216-224.
Not in our library10.1093/oxfordjournals.aje.a113992
- 133.
Vianna NJ, Kovasznay B, Polan A, Ju C. Infant leukemia and paternal exposure to motor vehicle exhaust fumes. J Occup Med. 1984;26:679-682.
Not in our library
- 134.
Watson GM. Leukaemia and paternal radiation exposure. Med J Aust. 1991;154:483-487.
Not in our library10.5694/j.1326-5377.1991.tb121186.x
- 135.
Westerbeek RM, Blair V, Eden OB, Kelsey AM, Stevens RF, Will AM, et al. Seasonal variations in the onset of childhood leukaemia and lymphoma. Br J Cancer. 1998;78:119-124.
Not in our library10.1038/bjc.1998.452
- 136.
Westergaard T. Birth characteristics, sibling patterns, and acute leukemia risk in childhood: a population-based cohort study. J Natl Cancer Inst. 1997;89:939-947.
Not in our library10.1093/jnci/89.13.939
- 137.
Wiemels JL, Leonard BC, Wang Y, Segal MR, Hunger SP, Smith MT, et al. Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA. 2002;99:15101-15106.
Not in our library10.1073/pnas.222481199
- 138.
Willis A, Lindahl T. DNA ligase deficiency in Bloom’s syndrome. Nature. 1987;325:355-357.
Not in our library10.1038/325355a0
- 139.
Woods WG, Roloff JS, Lukens JN, Krivit W. The occurrence of leukemia in patients with the Shwachman syndrome. J Pediatr. 1981;99:425-428.
Not in our library10.1016/s0022-3476(81)80336-8
- 140.
Yeazel MW, Buckley JD, Woods WG, Ruccione K, Robison LL. History of maternal fetal loss and increased risk of childhood acute leukemia at an early age, a report from the Childrens Cancer Group. Cancer. 1995;75:17180-1727.
Not in our library10.1002/1097-0142(19950401)75:7<1718::aid-cncr2820750725>3.0.co;2-g
- 141.
Yoshimoto Y, Kato H, Schull WJ. Risk of cancer among children exposed in utero to A-bomb radiations, 1950–84. Lancet. 1988;2:665-669.
Not in our library10.1016/s0140-6736(88)90477-1
- 142.
Yoshimoto Y, Neel JV, Schull WJ. Malignant tumors during the first 2 decades of life in the offspring of atomic bomb survivors. Am J Hum Genet. 1990;46:1041-1052.
Not in our library
- 143.
Zahm SH, Devesa SS. Childhood cancer: overview of incidence trends and environmental carcinogens. Environ Health Perspect. 1995;103:177-184.
Not in our library10.1289/ehp.95103s6177
- 144.
Zahm SH, Ward MH. Pesticides and childhood cancer. Environ Health Perspect. 1998;106:893-908.
Not in our library10.1289/ehp.98106893
- 145.
Zipf TF Berg S Roberts WM Poplack DG Steuber CP Bleyer WA 2000. Childhood leukemias. In: Clinical Oncology (Abeloff MD, Armitage JO, Lichter AS, Niederhuber JE, eds). 2nd ed. Philadelphia:Churchill Livingston, 2402–2429.
Not in our library
Cited by papers we hold 5
- Iron protects childhood acute lymphoblastic leukemia cells from methotrexate cytotoxicity · 2020Not checked
- Development and Clinical Translation of Approved Gene Therapy Products for Genetic Disorders · 2019No notice
- The burden of cancers and their variations across the states of India: the Global Burden of Disease Study 1990–2016 · 2018Corrected
- Volatile Organic Compounds in Air: Sources, Distribution, Exposure and Associated Illnesses in Children · 2018No notice
- Tobacco smoke and risk of childhood acute non-lymphocytic leukemia: findings from the SETIL study. · 2014Not checked
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.