Evidence map›Paper›PMID 30327567›Full record

ArticleBritish journal of cancer2018

Time to progression ratio in cancer patients enrolled in early phase clinical trials: time for new guidelines?

Sarah Watson, Jessica Menis, Capucine Baldini, Patricia Martin-Romano, Jean-Marie Michot, Antoine Hollebecque, Jean-Pierre Armand, Christophe Massard, Jean-Charles Soria, Sophie Postel-Vinay and 1 more

Abstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Efficacy assessment in phase I clinical trials: endpoints and challenges.Annals of oncology : official journal of the European Society for Medical Oncology · 2025
    Review
  5. Article
  6. Article
  7. Moving Molecular Profiling to Routine Clinical Practice: A Way Forward?Journal of the National Cancer Institute · 2020
    Article
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

11 authors.

Sarah WatsonDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Jessica MenisDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Capucine BaldiniDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Patricia Martin-RomanoDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Jean-Marie MichotDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Antoine HollebecqueDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Jean-Pierre ArmandDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Christophe MassardDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Jean-Charles SoriaDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Sophie Postel-VinayDrug Development Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France. sophie.postel-vinay@gustaveroussy.fr.
Xavier PaolettiBiostatistics and Epidemiology Department, Gustave Roussy Cancer Campus, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReliable evaluation of treatment benefit in early phase clinical trials is necessary. The time to progression ratio (TTPr), which compares successive TTP in a single patient, is a powerful criteria for determining targeted or immune therapies efficacy.

methodsWe evaluated 205 TTPr in a large cohort of 177 advanced cancer patients enrolled in at least two Phase 1/1b trials (out of 2827 phase 1/1b-treated patients) at Gustave Roussy.

resultsThis first wide description of TTPr showed that, under the hypothesis of overall absence of treatment line effect, the median TTPr was 0.7 and that 25% of patients presented a TTPr above the conventional efficacy threshold of 1.3.

conclusionsA higher median TTPr and a larger proportion of patients above the 1.3 threshold should therefore be achieved to conclude to drug efficacy. New guidelines for TTPr interpretation and calibration are proposed, which warrant independent prospective validation.

Indexed as

Disease ProgressionTreatment OutcomeAntineoplastic AgentsClinical Trials, Phase I as TopicHumansNeoplasmsAntineoplastic Agents

Identifiers

PMID30327567
PMCPMC6203755

What OpenQuestion holds

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LicenceCC BY
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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.