ArticleResearch synthesis methods2026
The hazards of using hazard ratios from proportional hazard models in indirect treatment comparisons.
Article in Research synthesis methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- A Matching-Adjusted Indirect Comparison of PET-Guided BrECADD Versus PET-Guided ABVD, BEACOPP, and eBEACOPP in Advanced Hodgkin Lymphoma.Advances in therapy · 2026Article
- Aligning Estimands to Strengthen the Credibility of Network Meta-Analysis: Implications for Indirect Treatment Comparisons.Statistics in biopharmaceutical research · 2026Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Indirect treatment comparison (ITC) is widely used to estimate the comparative effectiveness of treatments when head-to-head trials are unavailable. For the typical scenario of anchored ITC where one trial compares drug A to drug C (AC trial) and another compares drug B to drug C (BC trial), the comparative effectiveness of drugs A versus B is calculated by subtracting (or dividing) the relative treatment effect of A versus C in the AC trial by that of B versus C in the BC trial, assuming the covariate distributions in both trials are balanced. This operation is valid only if the chosen effect measure is transitive, that is, in a three-arm randomized trial of drugs A, B, and C, the direct treatment effect of A versus B equals the indirect treatment effect of A versus B through their comparisons to C. For survival outcomes, many ITCs use the hazard ratio (HR) as the effect measure. In this article, we demonstrate that HR is generally not transitive and should be used with caution. As more reliable alternatives, we recommend effect measures with better transitivity properties: the restricted mean survival time (RMST) difference, the landmark survival probability difference (or ratio) at a prespecified time point, and the average hazard with survival weights (AH-SW) difference.
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Registered trials
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