Evidence map›Paper›PMID 32913287›Full record

SynthesisBritish journal of cancer2020

A systematic review of meta-analyses assessing the validity of tumour response endpoints as surrogates for progression-free or overall survival in cancer.

Katy Cooper, Paul Tappenden, Anna Cantrell, Kate Ennis

Open access · hybridAbstract readSystematic Review
In one paragraph

Synthesis in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 10 pooled it
6.3field-weighted citation impact, top 2% of its field
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

37 citing papers in PubMed, 10 syntheses or guidelines pooled it, 86 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Katy CooperScHARR, University of Sheffield, Sheffield, UK. k.l.cooper@sheffield.ac.uk.ORCID http://orcid.org/0000-0002-7702-8103
Paul TappendenScHARR, University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0000-0001-6612-2332
Anna CantrellScHARR, University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0000-0003-0040-9853
Kate EnnisScHARR, University of Sheffield, Sheffield, UK.ORCID http://orcid.org/0000-0003-4284-217X
University of Sheffield · GB

Funding

Department of Health NIHR127852DH | National Institute for Health Research (NIHR) NIHR127852
6 · The paper itself

Abstract

backgroundTumour response endpoints, such as overall response rate (ORR) and complete response (CR), are increasingly used in cancer trials. However, the validity of response-based surrogates is unclear. This systematic review summarises meta-analyses assessing the association between response-based outcomes and overall survival (OS), progression-free survival (PFS) or time-to-progression (TTP).

methodsFive databases were searched to March 2019. Meta-analyses reporting correlation or regression between response-based outcomes and OS, PFS or TTP were summarised.

resultsThe systematic review included 63 studies across 20 cancer types, most commonly non-small cell lung cancer (NSCLC), colorectal cancer (CRC) and breast cancer. The strength of association between ORR or CR and either PFS or OS varied widely between and within studies, with no clear pattern by cancer type. The association between ORR and OS appeared weaker and more variable than that between ORR and PFS, both for associations between absolute endpoints and associations between treatment effects.

conclusionsThis systematic review suggests that response-based endpoints, such as ORR and CR, may not be reliable surrogates for PFS or OS. Where it is necessary to use tumour response to predict treatment effects on survival outcomes, it is important to fully reflect all statistical uncertainty in the surrogate relationship.

Indexed as

Clinical Trials as TopicProgression-Free SurvivalSurvivalTreatment OutcomeHumansMeta-Analysis as TopicNeoplasms

Identifiers

PMID32913287
PMCPMC7687906
OpenAlexW3084409173

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.