Profile and outcome of cancer patients enrolled in contemporary phase I trials.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
07 2023
Historique:
received: 14 03 2023
revised: 14 04 2023
accepted: 15 04 2023
medline: 19 6 2023
pubmed: 14 5 2023
entrez: 13 5 2023
Statut: ppublish

Résumé

Phase I trials historically involved heavily pretreated patients (pts) with no more effective therapeutic options available and with poor expected outcomes. There are scare data regarding profile and outcomes of pts enrolled into modern phase I trials. Here, we sought to provide an overview of pts' profile and outcome into phase I trials at Gustave Roussy (GR). This is a monocentric retrospective study, including all pts enrolled into phase I trials at GR from 2017 to 2021. Data regarding pts' demographics, tumour types, investigational treatments and survival outcomes were collected. In total, 9482 pts were referred for early phase trials; 2478 pts were screened, among which 449 (18.1%) failed screening; 1693 pts finally received at least one treatment dose as part of a phase I trial. Median age of pts was 59 years old (range, 18-88) and most common tumour types included gastrointestinal (25.3%), haematological (15%), lung (13.6%), genitourinary (10.5%) and gynaecologic cancers (9.4%). Amongst all pts treated and evaluable for response (1634 pts), objective response rate was 15.9% and disease control rate was 45.4%. Median progression-free survival and overall survival were, respectively, 2.6 months (95% confidence interval [95% CI], 2.3; 2.8) and 12.4 months (95% CI, 11.7; 13.6). As compared with historical data, our study shows that outcomes of pts included into modern phase I trials have improved and that these trials constitute nowadays a valid and safe therapeutic option. These updated data provide facts for adapting the methodology, role and place of phase I trials over the next years.

Sections du résumé

BACKGROUND
Phase I trials historically involved heavily pretreated patients (pts) with no more effective therapeutic options available and with poor expected outcomes. There are scare data regarding profile and outcomes of pts enrolled into modern phase I trials. Here, we sought to provide an overview of pts' profile and outcome into phase I trials at Gustave Roussy (GR).
METHODS
This is a monocentric retrospective study, including all pts enrolled into phase I trials at GR from 2017 to 2021. Data regarding pts' demographics, tumour types, investigational treatments and survival outcomes were collected.
RESULTS
In total, 9482 pts were referred for early phase trials; 2478 pts were screened, among which 449 (18.1%) failed screening; 1693 pts finally received at least one treatment dose as part of a phase I trial. Median age of pts was 59 years old (range, 18-88) and most common tumour types included gastrointestinal (25.3%), haematological (15%), lung (13.6%), genitourinary (10.5%) and gynaecologic cancers (9.4%). Amongst all pts treated and evaluable for response (1634 pts), objective response rate was 15.9% and disease control rate was 45.4%. Median progression-free survival and overall survival were, respectively, 2.6 months (95% confidence interval [95% CI], 2.3; 2.8) and 12.4 months (95% CI, 11.7; 13.6).
CONCLUSION
As compared with historical data, our study shows that outcomes of pts included into modern phase I trials have improved and that these trials constitute nowadays a valid and safe therapeutic option. These updated data provide facts for adapting the methodology, role and place of phase I trials over the next years.

Identifiants

pubmed: 37178645
pii: S0959-8049(23)00205-8
doi: 10.1016/j.ejca.2023.04.006
pii:
doi:

Types de publication

Clinical Trial, Phase I Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Emily Alouani (E)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France; Digestive Medical Oncology Department, IUCT-Rangueil, Toulouse Hospital University, Toulouse, France. Electronic address: alouani.e@chu-toulouse.fr.

Anas Gazzah (A)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: anas.gazzah@gustaveroussy.fr.

Sandrine Mercier (S)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: sandrine.mercier@gustaveroussy.fr.

Ratislav Bahleda (R)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: ratislav.bahleda@gustaveroussy.fr.

Antoine Hollebecque (A)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: antoine.hollebecque@gustaveroussy.fr.

Jean-Marie Michot (JM)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: jean-marie.michot@gustaveroussy.fr.

Capucine Baldini (C)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: capucine.baldini@gustaveroussy.fr.

Samy Ammari (S)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: samy.ammari@gustaveroussy.fr.

Stephane Champiat (S)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: stephane.champiat@gustaveroussy.fr.

Aurelien Marabelle (A)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: aurelien.marabelle@gustaveroussy.fr.

Sophie Postel-Vinay (S)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: sophie.postel-vinay@gustaveroussy.fr.

Vincent Ribrag (V)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: vincent.ribrag@gustaveroussy.fr.

Yohann Loriot (Y)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: yohann.loriot@gustaveroussy.fr.

Santiago Ponce Aix (SP)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: santiago.ponce@gustaveroussy.fr.

Linda Mahjoubi (L)

Drug Development Department (DITEP), Gustave Roussy Cancer Campus, Villejuif, France. Electronic address: linda.mahjoubi@gustaveroussy.fr.

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Classifications MeSH