Evidence map›Paper›PMID 40380280›Full record

ArticleJournal of translational medicine2025

Comparison of baseline patient characteristics in phase 1 and phase 2/3 clinical trials for anticancer treatments.

Maria Lucia Iacovino, Simone Talucci, Laura Arenare, Andrea Caglio, Andrea Canciello, Flavio Salerno, Sergio Facchini, Adriano Gravina, Clorinda Schettino, Maria Carmela Piccirillo and 3 more

Abstract readComparative Study
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Maria Lucia IacovinoNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Simone TalucciMenarini Ricerche SpA, via T. Speri 10, 00071, Pomezia, Italy.
Laura ArenareNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Andrea CaglioDepartment of Oncology, University of Turin, Ordine Mauriziano Hospital Umberto I, Largo Filippo Turati 62, 10128, Turin, Italy.
Andrea CancielloNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Flavio SalernoDepartment of Oncology, University of Turin, Ordine Mauriziano Hospital Umberto I, Largo Filippo Turati 62, 10128, Turin, Italy.
Sergio FacchiniNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Adriano GravinaNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Clorinda SchettinoNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Maria Carmela PiccirilloNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy.
Pier Paolo OlimpieriItalian Medicines Agency, via del Tritone 181, 00187, Rome, Italy.
Massimo Di MaioDepartment of Oncology, University of Turin, AOU Città della Salute e della Scienza di Torino, C.so Bramante 88, 10126, Turin, Italy.
Francesco PerroneNational Cancer Institute IRCCS Fondazione G.Pascale, via M. Semmola 52, 80131, Naples, Italy. f.perrone@istitutotumori.na.it.ORCID 0000-0002-9738-0526

Funding

Ministero della Salute Project L4/10
6 · The paper itself

Abstract

backgroundCharacteristics of patients significantly differ between registrational clinical trials (CTs) and Italian real-world practice, with older median age, higher elderly (≥ 65) rate and worse performance status (PS) in the latter, without imbalance in female rate. We compared the same characteristics between registrational phase 2/3 and phase 1 CTs.

methodsData on age, sex and PS were extracted from European Public Assessment Reports of European Medicines Agency. Weighted means and standard deviations were calculated in both groups and differences were described overall, by cancer type and drug class.

resultsWe collected 103 phase 2/3 and 111 phase 1 CTs, supporting 97 therapeutic indications. Age and sex were compared in 59 indications. Mean median age (SD) was 60.7 (5.1) years in phase 2/3 and 59.7 (5.6) years in phase 1 (p = 0.051). Age difference was greater for skin and breast cancer; no heterogeneity emerged among drug classes. Mean female rate was not statistically significantly lower in phase 2/3 than phase 1 CTs overall, (mean difference - 4.9%, p = 0.999); difference was greater for skin and upper-gastrointestinal cancers and for cytotoxic agents. Mean PS > 1 rate, compared in 47 indications, was similar in phase 2/3 [2.3% (4.7)] and phase 1 [1.8% (3.5)] (p = 0.374); difference was greater for colorectal cancer and cytotoxic agents.

conclusionsWe found no statistically significant difference in age, sex and PS between patients in phase 2/3 and corresponding phase 1 CTs for anticancer treatments. Therefore, patient selection in phase 1 trials appears crucial, considering its potential impact in later development phases.

Indexed as

Antineoplastic AgentsClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicNeoplasmsAgedFemaleHumansMaleMiddle AgedAntineoplastic AgentsAgeClinical trialsPerformance statusPhase 1Sex

Identifiers

PMID40380280
PMCPMC12083001

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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.