To the editor—We were interested to read Campbell and colleagues' timely network meta-analysis of antifungal therapies for HIV-associated cryptoccocal meningitis,recently published in the journal [1]. One of the authors' main conclusions is that the benefit of combination therapy with amphotericin B and flucytosine seems to be limited to individuals with altered consciousness at treatment initiation, and the discussion refers to our recent trial [2] to support this claim. However, it is important to note that the meta-analysis was based on study-level data only, and the covariate that was actually investigated was not whether an individual patient had altered consciousness, but whether the study included subjects with altered consciousness. Interpretation of population characteristics on the patient level is prone to the ecological fallacy, a well known risk of meta-regression analyses [3]. For example, our trial both included a relatively high proportion of subjects with altered consciousness and reported a significant mortality benefit of amphotericin B plus flucytosine compared with amphotericin B monotherapy [2]. However, it would be wrong to conclude that this indicates that the mortality benefit mainly applies to subjects with altered consciousness. Indeed, a subgroup analysis of our trial indicates that there is no evidence that the treatment effect depends on the Glasgow coma score (GCS), and, if anything, the subgroup effect in subjects with normal consciousness (GCS = 15) is even more convincing than in subjects with a GCS < 15 (Table 1).
Table 1.
Mortality at Day 14, Week 10 (Coprimary Endpoints) and Month 6 Overall and by GCS Score at Enrollment in the Vietnam Trial [2]
| Amphotericin B (N = 99) : Deaths/n (Mortality*) | Amphotericin B and Flucytosine (N = 100): Deaths/n (Mortality*) | Comparison: HR (95% CI), P Value | Test for Heterogeneity: P Value | |
|---|---|---|---|---|
| Death by day 14 | ||||
| All patients | 25/99 (25%) | 15/100 (15%) | 0.57 (.30–1.08), P = .08 | |
| GCS = 15 | 14/66 (21%) | 5/67 (7%) | 0.31 (.11–.87), P = .03 | |
| GCS < 15 | 11/31 (35%) | 10/32 (31%) | 0.90 (.38–2.12), P = .81 | .12 |
| Death by week 10 | ||||
| All patients | 44/99 (44%) | 30/100 (31%) | 0.61 (.38–.97), P = .04 | |
| GCS = 15 | 24/66 (36%) | 15/67 (23%) | 0.53 (.28–1.00), P = .05 | |
| GCS < 15 | 20/31 (65%) | 15/32 (48%) | 0.72 (.37–1.40), P = .33 | .57 |
| Death by month 6 | ||||
| All patients | 53/99 (54%) | 34/100 (35%) | 0.56 (.36–.86), P = .01 | |
| GCS = 15 | 32/66 (48%) | 18/67 (27%) | 0.46 (.26–.83), P = .01 | |
| GCS < 15 | 21/31 (68%) | 16/32 (51%) | 0.71 (.37–1.35), P = .30 | .42 |
Abbreviations: CI, confidence interval; GCS, Glasgow coma score; HR, hazard ratio (based on Cox regression).
*GCS at baseline was missing for 3 subjects. Mortality was estimated with the Kaplan-Meier estimator. Heterogeneity was tested with an interaction test between the subgrouping variable (GCS = 15 vs <15) and the treatment allocation. The amphotericin B plus fluconazole arm is not reported here.
More generally, we believe that our trial supports the use of amphotericin B plus flucytosine in populations with severe disease, as frequently seen in resource-limited settings, and we were pleased to read that the authors also endorse advocacy efforts to increase the availability of flucytosine in such settings. Although the presented network meta-analysis provides valuable aggregate evidence, it is our opinion that the evidence is not sufficiently strong to override the conclusions from our large and well designed trial, given the limitations cited by the authors regarding substantial heterogeneity between the included study populations, small sample sizes of many of the included studies, the inclusion of nonrandomized studies, and well recognized issues related to indirect comparisons [4]. However, we agree with the authors that the value of additional flucytosine in patients with less advanced disease than seen in our trial has not been established. Finally, we strongly agree with the author's conclusion that further well designed and adequately powered studies using clinical endpoints are required to improve the evidence base for determining the optimal treatment of patients with HIV-associated cryptococcal meningitis. It is important that these studies do not arbitrarily exclude “difficult to study” patients, such as those with severe disease, to ensure that study populations are representative of the general patient population and study findings are generalizable.
Acknowledgments
Financial support. This work was supported by the Wellcome Trust UK and the Medical Research Council/UK Department for International Development/Wellcome Trust Joint Global Health Trials Scheme (grant G1100684/1); J. N. D. is a Wellcome Trust Intermediate Fellow (award WT097147MA).
Potential conflict of interests. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
References
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