Evidence map›Paper›PMID 39555661›Full record

SynthesisMedical decision making : an international journal of the Society for Medical Decision Making2025

Multi-indication Evidence Synthesis in Oncology Health Technology Assessment: Meta-analysis Methods and Their Application to a Case Study of Bevacizumab.

Janharpreet Singh, Sumayya Anwer, Stephen Palmer, Pedro Saramago, Anne Thomas, Sofia Dias, Marta O Soares, Sylwia Bujkiewicz

Abstract readMeta-Analysis
In one paragraph

Synthesis in Medical decision making : an international journal of the Society for Medical Decision Making, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Visualization of Multi-indication Randomized Control Trial Evidence to Support Decision Making in Oncology: A Case Study on Bevacizumab.Medical decision making : an international journal of the Society for Medical Decision Making · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Janharpreet SinghBiostatistics Research Group, Department of Population Health Sciences, University of Leicester, Leicester, UK.ORCID 0000-0002-0272-3902
Sumayya AnwerCentre for Reviews and Dissemination, University of York, York, UK.
Stephen PalmerCentre for Health Economics, University of York, York, UK.
Pedro SaramagoCentre for Health Economics, University of York, York, UK.ORCID 0000-0001-9063-8590
Anne ThomasLeicester Cancer Research Centre, University of Leicester, Leicester, UK.
Sofia DiasCentre for Reviews and Dissemination, University of York, York, UK.ORCID 0000-0002-2172-0221
Marta O SoaresCentre for Health Economics, University of York, York, UK.ORCID 0000-0003-1579-8513
Sylwia BujkiewiczBiostatistics Research Group, Department of Population Health Sciences, University of Leicester, Leicester, UK.

Funding

Medical Research Council MR/W021102/1
6 · The paper itself

Abstract

backgroundMulti-indication cancer drugs receive licensing extensions to include additional indications, as trial evidence on treatment effectiveness accumulates. We investigate how sharing information across indications can strengthen the inferences supporting health technology assessment (HTA).

methodsWe applied meta-analytic methods to randomized trial data on bevacizumab, to share information across oncology indications on the treatment effect on overall survival (OS) or progression-free survival (PFS) and on the surrogate relationship between effects on PFS and OS. Common or random indication-level parameters were used to facilitate information sharing, and the further flexibility of mixture models was also explored.

resultsTreatment effects on OS lacked precision when pooling data available at present day within each indication separately, particularly for indications with few trials. There was no suggestion of heterogeneity across indications. Sharing information across indications provided more precise estimates of treatment effects and surrogacy parameters, with the strength of sharing depending on the model. When a surrogate relationship was used to predict treatment effects on OS, uncertainty was reduced only when sharing effects on PFS in addition to surrogacy parameters. Corresponding analyses using the earlier, sparser (within and across indications) evidence available for particular HTAs showed that sharing on both surrogacy and PFS effects did not notably reduce uncertainty in OS predictions. Little heterogeneity across indications meant limited added value of the mixture models.

conclusionsMeta-analysis methods can be usefully applied to share information on treatment effectiveness across indications in an HTA context, to increase the precision of target indication estimates. Sharing on surrogate relationships requires caution, as meaningful precision gains in predictions will likely require a substantial evidence base and clear support for surrogacy from other indications. HIGHLIGHTS: We investigated how sharing information across indications can strengthen inferences on the effectiveness of multi-indication treatments in the context of health technology assessment (HTA).Multi-indication meta-analysis methods can provide more precise estimates of an effect on a final outcome or of the parameters describing the relationship between effects on a surrogate endpoint and a final outcome.Precision of the predicted effect on the final outcome based on an effect on the surrogate endpoint will depend on the precision of the effect on the surrogate endpoint and the strength of evidence of a surrogate relationship across indications.Multi-indication meta-analysis methods can be usefully applied to predict an effect on the final outcome, particularly where there is limited evidence in the indication of interest.

Indexed as

BevacizumabTechnology Assessment, BiomedicalAntineoplastic Agents, ImmunologicalHumansMedical OncologyNeoplasmsProgression-Free SurvivalRandomized Controlled Trials as TopicAntineoplastic Agents, ImmunologicalBevacizumabhealth technology assessmentmeta-analysismixture modelsmulti-indication drugsoncologysurrogate endpoints

Identifiers

PMID39555661
PMCPMC11645851

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.