Systematic review of influenza resistance to the neuraminidase inhibitors

1Influenza (the flu) is an acute infection of the upper respiratory tract which is transmitted via respiratory droplets and direct contact. Immunocompromised people and those with underlying cardio-pulmonary conditions are considered at increased risk from serious influenza-related complications. Annually, influenza infection results in more than 500, 000 deaths worldwide. The influenza virus is an RNA virus that belongs to the Orthomyxoviridae family. There are two main types of influenza virus: type A and type B. These two types are responsible for seasonal flu epidemics each year. The influenza virus is continually evolving and under immune pressure; it may either evolve through small gradual changes in the virus (antigenic drift) or through abrupt major changes in the virus (antigenic shift) most frequently by genetic reassortments. Such changes can result in the emergence of new influenza viruses that can cause pandemics (e.g., the 1918 Spanish flu pandemic and the 2009 H1N1 pandemic).

2Vaccines play a critical role in the prevention of influenza. Nevertheless, the efficacy of this intervention could be significantly reduced owing to a mismatch between the seasonal influenza vaccine and the circulating influenza virus and the inability of the host to mount a proper immune response. Therefore, antivirals also play an important role in the prevention and management of influenza. There are two classes of antiviral agents for influenza: adamantanes and neuraminidase inhibitors. Adamantanes (amantadine and rimantadine), however, are not recommended alone for the treatment of influenza due to their lack of activity against influenza B and the high level of influenza A resistance. Neuraminidase inhibitors (NAIs) are effective against all human, avian and animal influenza viruses. NAIs inhibit the release of virions by competitively inhibiting viral NA, which is a key glycoprotein at the surface of the virus. Currently there are two NAIs drugs which have been approved worldwide: Oseltamivir (Tamiflu®) and Zanamivir (Relenza®). Both drugs are approved for treatment of acute uncomplicated illness due to influenza A and B, and are also approved for preventive use. Oseltamivir is provided orally to persons older than one year who have been symptomatic for no more than 2 days. Zanamivir is provided as a dry powder which is given by inhalation in persons aged 7 years and older who have been symptomatic for no more than 2 days.

3Peramivir is an intravenous neuraminidase inhibitor under development for the treatment of influenza. In October 2009, the FDA issued an Emergency Use Authorization (EUA) for the use of peramivir based on safety data from Phase 1, Phase 2 trials, and limited Phase 3 trial data. The EUA for peramivir expired in June 2010. However, peramivir has been approved in Japan and Korea. More recently, laninamivir, a long-lasting inhaled neuraminidase inhibitor has also been licensed in Japan.

4Influenza A and B strains had remained susceptible to oseltamivir with rare exceptions since their availability in 1999. Recent reviews and expert opinions have identified studies reporting prevalence and incidence rates of antiviral resistance among patients treated with oseltamivir. Until recently, the prevalence of antiviral resistance had been relatively low. However, in the influenza season 2008-2009, the Centers for Disease Control and Prevention (CDC) reported a worldwide significant increase in the prevalence of oseltamivir resistance to influenza A/H1N1 viruses (A/Brisbane/59/2007-like strains) due to the H275Y NA mutation. Furthermore, about 1% of tested 2009 pandemic H1N1 viruses (A/California/07/2009 (H1N1) - like strain) were found to be resistant to oseltamivir due to the same mutation. Finally, a Japanese study published in 2004 reported incidence of antiviral resistance in hospitalized children as high as 18%.

5To date influenza A and B, including all types of A/H1N1 virus, remain susceptible to zanamivir. Further, a recent review only found one documented case of zanamivir resistance. Oseltamivir is easier to administer and has therefore been used vastly more than zanamivir. For this reason, most literature on antiviral resistance associated with NAIs has only investigated antiviral resistance associated with oseltamivir. However, owing to the higher resistance rates associated with oseltamivir, especially for A/H1N1 strains between 2007-09, zanamivir has been increasingly utilized for the treatment and prevention of influenza. Therefore, there is a need to investigate the development of influenza resistance to zanamivir in this time period. Studies investigating resistance to peramivir may also have emerged.

6We therefore conducted a systematic review using comprehensive literature search strategies to identify and systematically assess all relevant studies on antiviral resistance associated with oseltamivir, zanamivir, and peramivir.

7Our primary objective was to systematically review the literature to determine the incidence of resistance to oseltamivir, zanamivir, and peramivir in adult immunocompetent outpatients for the prevention and treatment of influenza. We did not consider lananimivir since it was not licensed at the time we commenced this review.

8Our secondary objectives were to

91) Systematically review data from the literature to determine the incidence of resistance to oseltamivir, zanamivir, and peramivir in different patient populations (e.g., hospitalized, immunocompromised, children, and others).

102) Assess the clinical consequences of antiviral resistance (clinical complications and symptoms associated with antiviral resistance, and severity of complications and symptoms among resistant patients).

11We included randomized clinical trials (RCTs), cohort and case-control studies, and case reports.

12We included adult immunocompetent outpatients for our primary objective. For our secondary objective we included patients if they were children, immunocompromised, or hospitalized.

13We included studies that reported incidence of antiviral resistance associated with one or more of the three NAIs oseltamivir, zanamivir, and peramivir. We included all studies regardless of the dose and length of follow-up. We did not include studies where an NAI was administered in combination with another antiviral (e.g., rimantadine)

14Our primary and first secondary outcome of interest was incidence of antiviral resistance and our secondary outcomes of interest were the clinical consequences associated with antiviral resistance.

15Viral resistance is detected either by the presence of resistance-associated mutations such as the H274Y (N2 numbering) or H275Y (N1 numbering) substitution or by measuring the median 50% inhibitory concentration (IC50). Commonly used laboratory criteria for determining known antiviral resistance is a substantially elevated IC50 value by enzyme inhibition assay (a value greater than 10-fold that of the corresponding parent virus or greater than three standard deviation (SD) compared to the mean value. For example, for the H1N1 virus with the most frequent H275Y NA mutation, the observed IC50 values are usually 200- 400 fold higher than the mean IC50 value. However, the definition of antiviral resistance is not standardized and could differ for each of the three NAIs, and may also vary across included studies (due to pre-specification of a threshold or different assays). For that reason, we used the definition of resistance as outlined in the studies to determine the incidence of antiviral resistance.

16Measured influenza outcomes included duration of antiviral shedding, the peak viral titers, and the days to resolution of influenza symptoms. For studies reporting on clinical consequences of antiviral resistance, we reported all influenza related complications and symptoms.

17We searched MEDLINE and EMBASE without language restrictions in September 2010. We limited the search strategy to human studies. We also manually searched reference lists from recent review articles.

18Two reviewers (KT and TA) independently reviewed the abstracts for potential eligibility and subsequently full text publications for eligibility. Disagreements were resolved by discussion.

19We extracted a number of variables on study design and methodological characteristics, patient and intervention characteristics, and outcomes from all eligible studies (see appendix). Data extraction was done independently by two reviewers (KT and TA) and disagreements were resolved by discussion.

20For the RCTs, we assessed the adequacy of the methods used for randomization, allocation concealment, blinding, and follow-up. We scored the quality for each RCT by assigning one point for each adequate item. With this scale, RCTs can score a minimum of 0 points and a maximum score 4 points. We considered RCTs that scored at least 3 points as high quality. We used the Newcastle-Ottawa Scale (NOS) to assess the adequacy of the employed methodology in the retrieved observational studies. For observational studies reporting incidence of antiviral resistance, there were no control groups. We therefore used a modified version of the NOS scale for cohort studies, taking out the three items that dealt with adequacy of controls or comparison between exposed and non-exposed individuals. With this scale, incidence studies can score a minimum of 0 points and a maximum of 6 points. We considered studies that scored at least 5 points as high quality. For observational studies reporting on consequences of antiviral resistance, we used the complete NOS scale. With this scale, incidence studies can score a minimum of 0 points and a maximum of 9 points. We considered studies that scored at least 7 points as high quality.

21We calculated the antiviral resistance incidence rate and the associated 95% confidence interval (CI) for all studies and study subgroups. Antiviral resistance incidence rate was calculated as the proportion of patients who developed resistance. We calculated the 95% CI based on the assumption that the incidence rate followed a binomial distribution. For incidence rates equal to 0%, we used the "rule of threes" to calculate the upper 95% CI upper bound. This rule says that the 95% CI upper bound is equal to 3/n, where n is the sample size.

22We calculated the antiviral resistance incidence rate and the associated 95% CI for all studies (and subgroups) involving immunocompetent adult out-patients. We produced forest plots and pooled incidence rates across studies using the arcsine method.

23We first performed subgroup analysis on type of NAIs (oseltamivir, zanamivir, or peramivir) and pooled incidence rates within each subgroup using the arcsine method. For each type of NAIs, we then performed subgroup analyses for study design, type of influenza, immunocompetent/immunocompromised patients, out patients/hospitalized patients, adults/children, and prophylaxis/treatment and produced corresponding forest plots. We did not produce pooled estimates in these subgroups.

24We qualitatively compared the mean, median, minimum, and maximum duration of antiviral shedding, the peak viral titers, and the days to resolution of influenza symptoms reported in the identified incidence studies.

25We reported odds ratios and risk ratios for associations between antiviral resistance and clinical complications or symptoms. Whenever possible, these ratios were combined in a random-effects meta-analysis and presented in a forest plot. Adjusted ratios obtained from multivariate models were preferred to crude ratios. If possible, risk ratios were converted to odds ratios.

26For resistant patients reported in case reports, we created a qualitative overview (a table) of clinical complications (e.g., pneumonia) and symptoms which authors believed could be associated with resistance.

27Our search resulted in 1289 hits after removal of duplicate citations. Figure 1 presents the PRISMA diagram for our eligibility scan. A total of 43 study reports were eligible. Among these, ten were randomized clinical trials (RCTs) that reported incidence of antiviral resistance, (effectively fourteen since two publications reported results from four and three RCTs respectively) and nine were cohort studies that reported incidence of antiviral resistance. Four were case-control studies that reported associations between antiviral resistance and clinical symptoms or complications. Lastly, 21 were case reports comprising reports on a total of 27 patients. None of the ten RCTs or the nine cohort studies made head to head comparisons between any two of the three NAIs (i.e., all 19 studies only included one NAI arm). Thirteen studies measured incidence of antiviral resistance among subjects given oseltamivir,, five studies measured incidence of antiviral resistance among subjects given zanamivir, and only one study measured incidence of antiviral resistance among subjects given peramivir. Four oseltamivir studies and all zanamivir and peramivir studies were RCTs. The four association studies all estimated associations between oseltamivir resistance and clinical complications and symptoms. Among the 21 case reports, 17 reported on resistance to oseltamivir only, and 2 on resistance to zanamivir only, and 2 on resistance to both. In 12 of the 21 case reports (13 out of 27 patients) where oseltamivir was the initial treatment, patients were eventually switched to zanamivir.

28Most studies that reported incidence of antiviral resistance included a mix of our pre-specified subgroups. The methodological quality, the patient characteristics, and the intervention characteristics of the incidence studies are presented in table 1. All RCTs were of high quality. Only one incidence study was low quality according to the modified NOS. The four case-control studies that reported associations between antiviral resistance and clinical symptoms and complications all scored between 7/9 and 9/9 on the NOS.

29Most studies included a mix of the considered subgroups but did report results separately for each subgroup. It was therefore only possible to extract data from five studies for our primary objective: incidence of resistance among adult immunocompetent out-patients. Among these five studies, one reported incidence of antiviral resistance associated with oseltamivir, three reported incidences of antiviral resistance associated with zanamivir, and one reported incidences of antiviral resistance associated with peramivir. In all five studies, patient recruitment ended in or before year 2000. Incidence of resistance was 0% in all five studies. For this reason we did not produce a forest plot.

30Figure 2 shows the incidence of antiviral resistance subgrouped by NAI (oseltamivir, zanamivir, and peramivir). The pooled incidence rate for oseltamivir was 2.6% (95%CI 0.7% to 5.5%). However, the estimated heterogeneity was I2 = 90%. The incidence rate for all zanamivir studies was 0%. All zanamivir studies were RCTs. Further, all zanamivir studies ended in or before year 2000. Only one study measured incidence of antiviral resistance among subjects given peramivir and was reported to be 0%.

31Because antiviral resistance was only observed in oseltamivir studies, we did not produce subgroup forest plots including zanamivir or peramivir studies. Figure 3 presents the forest plot of incidence of antiviral resistance to oseltamivir subgrouped by influenza type. The remaining subgroup forest plots of incidence of antiviral resistance are presented in additional files 1, 2, 3, 4 and 5 (figures A.1 to A.5).

32Antiviral resistance was observed among A/H1N1 patients in 5 of 6 studies with incidence rates varying from 3.6% and 27.3%. Among influenza A/H3N2 patients, incidence rates across three studies were 0%, 3.3%, 18%. Incidence rates among influenza B patients were 0% in two studies and 2% in one study (see figure 3). Antiviral resistance rates in prophylaxis studies were either 0% or low (4%), whereas more than half of the treatment studies reported resistance rates above 5% (see additional file 1, figure A.1).

33Our subgroup analyses on RCTs versus observational studies, immunocompetent versus immunocompromised, out-patients versus in-patients, and adults versus children did not yield any apparent differences between subgroups. The lack of apparent differences was, in part, due to the large degree of heterogeneity within subgroups. All remaining subgroup analyses are presented in the appendices (see additional files 2, 3, 4 and 5 (figures A.2-A.5)).

34Figure 4 shows the forest plot of risk ratios for association between oseltamivir resistance and clinical complications that were reported in more than one study. The meta-analysis of the association between oseltamivir-resistance and pneumonia yielded a statistically significant risk ratio (RR 4.16, 95% CI 1.28 to 13.1, p = 0.02). The meta-analyses of the association with otitis yielded a pooled risk ratio of 0.97 (95% CI 0.41 to 2.43). The meta-analysis of the association with hospitalization yielded a pooled risk ratio of 0.60 (95% CI 0.24 to 1.48). The study by Hauge additionally reported adjusted risk ratios for the associations with sinusitis (RR 1.7, 95% CI 0.4 to 7.5) and with bronchitis (RR 0.8, 95% CI 0.4 to 1.8). Two deaths were reported in the study by Dharan. However, these two patients died before they were admitted to the hospital. No deaths were reported in the other three identified association studies.

35The meta-analyses of associations between oseltamivir resistance and the clinical symptoms (cough, fever, sore throat, myalgia, acute/sudden onset, runny nose and headache), did not reveal any differences between oseltamivir-resistant and oseltamivir-susceptible patients. All pooled risk ratio estimates were equal or very close to 1.00 and all 95% CIs included 1.00. The forest plots for these meta-analyses are presented in additional file 6 and 7 (figure A.6). One study (Dharan) additionally reported odds ratios on chills and breathing difficulty. Risk ratio estimates for these two symptoms were close to 1.00 and had wide confidence intervals.

36Table 2 provides a summary of the duration of illness reported across association and incidence studies. Overall, the oseltamivir-resistant and oseltamivir-susceptible patients seem to require the same number of days to reach resolution of symptoms.

37The identified case reports showed a wide spectrum of complications associated with antiviral resistance. Table 3 summarized these complications in relation to the type of treatment, patient group and influenza. The complications associated with antiviral resistance were typically of a respiratory nature. Prolonged fever was also common. In 9 case reports, oseltamivir resistant patients were switched to zanamivir once viral resistance had been detected. In some cases, patients seemed to recover as a result of the switch, in others cases they did not.

38The primary focus of this review was to describe the incidence of resistance to oseltamivir, zanamivir, and peramivir in adult immunocompetent outpatients for the prevention and treatment of influenza. However, we did not identify sufficient evidence to draw any conclusions about this issue. The secondary focus of our review was to describe the incidence and consequences of antiviral resistance across various population groups. Overall the incidence of oseltamivir-resistance across studies was 2%. We found higher oseltamivir-resistance incidence rates among influenza A patients - particularly those of the H1N1 subtype. Zanamivir was associated with 0% incidence of resistance. Only one study measured incidence of antiviral resistance among subjects given peramivir and it was reported to be 0%. However, zanamivir and peramivir clinical trials stopped enrolling in year 2000 at the latest, and therefore have little generalizability. We did not compare the incidence rates between drugs because there are no head-to-head studies that have compared these drugs. Our analyses of consequences associated with development of antiviral resistance demonstrated that oseltamivir-resistant patients are approximately 4 times more likely to suffer from pneumonia than oseltamivir-susceptible patients. We did not find any associations between oseltamivir-resistance and other clinical complications or symptoms. We did not identify any studies reporting on association between zanamivir or peramivir resistance and clinical complications or symptoms. Our review of case reports shows that antiviral resistance can be associated with a number of serious complications. Such complications are typically of a respiratory nature and may in some cases be so severe that the patient will die, but whether it depends on viral resistance or on the host's immune response needs to be determined.

39Our review comes with a number of strengths and limitations. We collectively reviewed randomized clinical trials, cohort studies, case series, and case reports. Randomized clinical trials are typically conducted under controlled settings that may not be entirely representative of general clinical practice. In the context of our review, such controlled settings may substantially reduce the risk of developing antiviral resistance. By including observational studies in our review, we obtain incidence estimates that are generalizable to conventional clinical practice settings. Furthermore, our additional inclusion of case reports allowed us to evaluate the severity of the clinical complications that can arise from antiviral resistance.

40Despite including a wide range of considered study designs, our review finds its limitations in the paucity of evidence. We did not find any recent studies that investigated incidence of antiviral resistance associated with zanamivir or peramivir, in fact, all studies on zanamivir ended patients' recruitment in 2000 at the latest. Thus, we were unable to assess whether zanamivir and peramivir still yields a (close to) 0% incidence of antiviral resistance. In addition to the time factor, it is reported that there is a cross-resistance association between oseltamivir and peramivir. For patients infected with A/H1N1 virus harboring the H275Y mutation, studies conducted before the 2007-2009 seasons are therefore likely to underestimate resistance to peramivir dramatically. Furthermore, recent peramivir clinical trials have evaluated a parenteral injection form instead of prior oral tablets.

41Most oseltamivir studies included a mix of population subgroups and had little or no reporting on subgroup results. As a result, much within-subgroup heterogeneity ensued, and thus, many of our subgroup analyses did not yield any 'apparent' differences. The presence of a mixture of resistant and susceptible viruses especially in immunocompromised hosts may also potentially complicate the interpretation of our findings. Lastly, we did not find any studies on incidence of antiviral resistance among H5N1 patients, and only two case reports on H5N1 patients. As for case reports, it is likely that our search may have missed a substantial number of case reports due to such publications being poorly indexed in the utilized search engines. We excluded some case reports of oseltamivir resistance in H5N1 infected humans because no clinical data was reported or because resistance was detected pre-therapy.

42The rates at which pneumonia occurred in oseltamivir-susceptible patients were between 1% and 3%. Meanwhile, our meta-analysis suggests that oseltamivir-resistant patients are 4-times more likely to suffer from pneumonia. Assuming that 2% of oseltamivir-susceptible patients suffer from pneumonia, 1 out of every 50 oseltamivir-susceptible patients would suffer from pneumonia in comparison to 1 out of every 12 oseltamivir-resistant patients. It is noteworthy that in the identified case reports, many cases of resistance arose in immunocompromised patients adding a confounder in the interpretation of this association.

43Our review provides valuable insight on the incidence of antiviral resistance associated with oseltamivir use. However, we were not able to draw inferences about incidence of antiviral resistance associated with zanamivir or peramivir use due to the absence of recent studies on the topic. The reviewed case reports mainly involved immunocompromised subjects who were hospitalized (in-patients) and received oseltamivir as treatment rather than prophylaxis. This could suggest a tendency that notable complications associated with antiviral resistance more frequently arise among such patients. To confirm this, however, future cohort studies that investigate the associations between antiviral resistance and complications should incorporate patient and treatment characteristics in the multivariate models.

44Our results demonstrate that that a substantial number of patients may become oseltamivir-resistant as a result of oseltamivir use, and that oseltamivir resistance may be significantly associated with pneumonia. In contrast, zanamivir resistance has been rarely reported to date.

45This review was funded by GlaxoSmithKline Inc. (GSK).

46Lehana Thabane (LT) has received consultancies from several pharmaceutical companies including GSK, AstraZeneca, CanReg Inc., F. Hoffman La Roche, Theralase Inc, Sorono Canada Inc, Merck Frosst - Schering Pharmaceuticals, Pfizer, Proctor and Gamble Pharmaceuticals, and law firms that include Newton Wong and Associates, and Paterson McDougall.

47Guy Boivin (BG) has received research grants and honoraria from GSK and Hoffman La Roche.

48Tahany Awad (TA) has received consultancies from Hoffman La Roche.

49Kristian Thorlund (KT) has no financial interests to declare.

50The authors declare that they have no competing interests.

51KT drafted the protocol and the manuscript, assessed eligibility of identified study abstracts, extracted data, scored the quality of all eligible studies and performed all statistical analyses. TA contributed to the writing of the protocol and the manuscript, contributed to the design of the review, contributed to the interpretation of data, assessed eligibility of identified study abstracts, extracted data and scored the quality of all eligible studies. GB and LT contributed the writing of the protocol and manuscript, contributed to the design of the review and contributed to the interpretation of data.

52All authors read and approved the final version of the manuscript.

53The pre-publication history for this paper can be accessed here:

54http://www.biomedcentral.com/1471-2334/11/134/prepub