Evidence map›Paper›PMID 36199019›Full record

ArticleBMC medical research methodology2022

The case against censoring of progression-free survival in cancer clinical trials - A pandemic shutdown as an illustration.

Corinne Jamoul, Laurence Collette, Elisabeth Coart, Koenraad D'Hollander, Tomasz Burzykowski, Everardo D Saad, Marc Buyse

Abstract read
In one paragraph

Article in BMC medical research methodology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Corinne JamoulInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium. corinne.jamoul@hotmail.com.
Laurence ColletteInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium.
Elisabeth CoartInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium.
Koenraad D'HollanderInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium.
Tomasz BurzykowskiInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium.
Everardo D SaadInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium.
Marc BuyseInternational Drug Development Institute (IDDI), Av. Provinciale, 30 - 1340, Louvain-la-Neuve, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMissing data may lead to loss of statistical power and introduce bias in clinical trials. The Covid-19 pandemic has had a profound impact on patient health care and on the conduct of cancer clinical trials. Although several endpoints may be affected, progression-free survival (PFS) is of major concern, given its frequent use as primary endpoint in advanced cancer and the fact that missed radiographic assessments are to be expected. The recent introduction of the estimand framework creates an opportunity to define more precisely the target of estimation and ensure alignment between the scientific question and the statistical analysis.

methodsWe used simulations to investigate the impact of two basic approaches for handling missing tumor scans due to the pandemic: a "treatment policy" strategy, which consisted in ascribing events to the time they are observed, and a "hypothetical" approach of censoring patients with events during the shutdown period at the last assessment prior to that period. We computed the power of the logrank test, estimated hazard ratios (HR) using Cox models, and estimated median PFS times without and with a hypothetical 6-month shutdown period with no patient enrollment or tumor scans being performed, varying the shutdown starting times.

resultsCompared with the results in the absence of shutdown, the "treatment policy" strategy slightly overestimated median PFS proportionally to the timing of the shutdown period, but power was not affected. Except for one specific scenario, there was no impact on the estimated HR. In general, the pandemic had a greater impact on the analyses using the "hypothetical" strategy, which led to decreased power and overestimated median PFS times to a greater extent than the "treatment policy" strategy.

conclusionAs a rule, we suggest that the treatment policy approach, which conforms with the intent-to-treat principle, should be the primary analysis to avoid unnecessary loss of power and minimize bias in median PFS estimates.

Indexed as

COVID-19NeoplasmsDisease-Free SurvivalHumansPandemicsProgression-Free SurvivalResearch DesignBiasCensoringEstimandsPandemicPowerProgression-free survival

Identifiers

PMID36199019
PMCPMC9532825

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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.