Evidence map›Paper›PMID 35533427›Full record

ArticleESMO open2022

Access to early-phase clinical trials in older patients with cancer in France: the EGALICAN-2 study.

C Baldini, E Charton, E Schultz, L Auroy, A Italiano, M Robert, E Coquan, N Isambert, P Moreau, S Le Gouill and 12 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Inequities in enrollment across clinical trial phases and the need for a Spanish perspective.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

22 authors at 16 institutions in 3 countries.

C BaldiniGustave Roussy, Université Paris-Saclay, Drug Development Department (DITEP), Villejuif; Laboratory for Immunomonitoring in Oncology (LIO), University Paris-Saclay, Gustave Roussy Cancer Campus, Villejuif. Electronic address: capucine.baldini@gustaveroussy.fr.
E ChartonHuman and Social Sciences Department, Centre Léon Bérard, Lyon.
E SchultzCEPED (UMR 196), Université de Paris, IRD, Paris; SESSTIM, Sciences Economiques & Sociales de la Santé & Traitement de l'Information Médicale, CANBIOS Team (Équipe Labellisée LIGUE 2019), Aix-Marseille University, INSERM, IRD, Marseille.
L AuroyUniversité Grenoble Alpes, CNRS, Sciences Po Grenoble, Pacte, Grenoble.
A ItalianoInstitut Bergonié, Early Phase Trials and Sarcoma Units, Bordeaux; University of Bordeaux, Bordeaux.
M RobertInstitut de Cancérologie de l'Ouest, Medical Oncology Department, Saint-Herblain.
E CoquanFrançois Baclesse Cancer Center, Department of Oncology, Caen.
N IsambertDépartement d'Innovations Thérapeutiques/recherche Translationnelle en Oncologie et Hématologie (DITTOH), INSERM U1084, CHU de Poitiers, Poitiers.
P MoreauCentre GF Leclerc, Medical Oncology Department, Dijon.
S Le GouillService d'Hématologie Clinique, Unité d'Investigation Clinique, CHU, Nantes.
C Le TourneauDepartment of Drug Development and Innovation, Institut Curie, Paris-Saclay University, Paris & Saint-Cloud.
Z GhriebAPHP, Hopital Saint-Louis, Centre d'Investigations Cliniques, Paris.
J J KiladjianDepartment of Medicine & Clinical Research Unit, Institut Claudius Regaud/Institut Universitaire du Cancer de Toulouse (IUCT-Oncopole), Toulouse.
J P DelordDepartment of Medicine & Clinical Research Unit, Institut Claudius Regaud/Institut Universitaire du Cancer de Toulouse (IUCT-Oncopole), Toulouse.
C Gomez RocaDepartment of Medicine & Clinical Research Unit, Institut Claudius Regaud/Institut Universitaire du Cancer de Toulouse (IUCT-Oncopole), Toulouse.
N VeyAix-Marseille University, CNRS, Inserm, Institut Paoli-Calmettes, Hematology Department, CRCM, Marseille.
F BarlesiAix Marseille University, CNRS, INSERM, CRCM, APHM, Marseille Early Phases Cancer Center CLIP(2), Marseille; Gustave Roussy, Université Paris-Saclay, Villejuif.
T LesimpleClinical Research Department, CLIP(2) and ARPEGO Network, Rennes.
N PenelCLIP(2) Lille, Centre Oscar Lambret, Lille and Lille University, Lille.
J C SoriaGustave Roussy, Université Paris-Saclay, Villejuif.
C MassardGustave Roussy, Université Paris-Saclay, Drug Development Department (DITEP), Villejuif.
S BesleGustave Roussy, Université Paris-Saclay, Drug Development Department (DITEP), Villejuif; Laboratory for Immunomonitoring in Oncology (LIO), University Paris-Saclay, Gustave Roussy Cancer Campus, Villejuif; Lyon 1 University, EA4129, Lyon, France.
Université Paris-Saclay · FRInstitut Claudius Regaud · FRInserm · FRAix-Marseille Université · FRCentre d'Investigation Clinique de Nantes · FRCentre François Baclesse · LUCentre Georges François Leclerc · FRCentre Léon Bérard · FRCentre National de la Recherche Scientifique · FRCentre Oscar Lambret · FREconomic & Social Sciences, Health Systems & Medical Informatics · FRHôpital Saint-Louis · FRInstitut de Cancérologie de l'Ouest · FRInstitut Gustave Roussy · FRResearch Network (United States) · USUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccess to clinical trials and especially early-phase trials (ECT) is an important issue in geriatric oncology. As cancer can be considered an age-related disease because the incidence of most cancers increases with age, new drugs should also be evaluated in older patients to assess their safety and efficacy. The EGALICAN-2 study was primarily designed to identify social and/or regional inequalities regarding access to ECT. We focused on the factors of inequalities in access to ECT in older patients. PATIENTS AND

methodsDuring a 1-year period (2015-2016), a survey was conducted in 11 early-phase units certified by the French National Cancer Institute.

resultsA total of 1319 patients were included in the analyses: 1086 patients (82.3%) were <70 years and 233 patients (17.7%) were >70 years. The most common tumor types at referral in older patients were gastrointestinal (19.3%), hematological (19.3%), and thoracic tumors (18.0%). Most patients referred to the phase I unit had signed informed consent and the rate was similar across age (92.7% in younger patients versus 90.6% in older patients; P = 0.266). The rate of screening failure was also similar across age (28.5% in younger patients versus 24.3% in older patients; P = 0.219). Finally, in older patients, univariate analyses showed that initial care received in the hospital having a phase I unit was statistically associated with first study drug administration (odds ratio 0.49, 90% confidence interval 0.27-0.88; P = 0.045).

conclusionsOlder patients are underrepresented in early clinical trials with 17.7% of patients aged ≥70 years compared with the number of new cases of cancer in France (50%). However, when invited to participate, older patients were prone to sign informed consent.

Indexed as

NeoplasmsAgedClinical Trials as TopicFranceHumansIncidenceaccesscancerearly-phase clinical trialsenrollmentolder patients

Identifiers

PMID35533427
PMCPMC9271476
OpenAlexW4229055066

What OpenQuestion holds

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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.