Expanding Access to Lung Cancer Clinical Trials by Reducing the Use of Restrictive Exclusion Criteria: Perspectives of a Multistakeholder Working Group.

Cancer clinical trials Eligibility criteria Expanded access Non–small-cell lung cancer Small-cell lung cancer

Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
07 2020
Historique:
received: 17 11 2019
revised: 02 02 2020
accepted: 13 02 2020
pubmed: 24 3 2020
medline: 6 7 2021
entrez: 24 3 2020
Statut: ppublish

Résumé

Low rates of adult patient participation have been a persistent problem in cancer clinical trials and have continued to be a barrier to efficient drug development. The routine use of significant exclusion criteria has contributed to this problem by limiting participation in studies and creating significant clinical differences between the study cohorts and the real-world cancer patient populations. These routine exclusions also unnecessarily restrict opportunities for many patients to access potentially promising new therapies during clinical development. Multiple efforts are underway to broaden eligibility criteria, allowing more patients to enroll in studies and generating more robust data regarding the effect of novel therapies in the population at large. Focusing specifically on lung cancer as an example, a multistakeholder working group empaneled by the LUNGevity Foundation identified 14 restrictive and potentially outdated exclusion criteria that appear frequently in lung cancer clinical trials. As a part of the project, the group evaluated data from multiple recent lung cancer studies to ascertain the extent to which these 14 criteria appeared in study protocols and played a role in excluding patients (screen failures). The present report describes the working group's efforts to limit the use of these routine exclusions and presents clinical justifications for reducing the use of 14 criteria as routine exclusions in lung cancer studies, potentially expanding trial eligibility and improving the generalizability of the results from lung cancer trials.

Identifiants

pubmed: 32201247
pii: S1525-7304(20)30033-4
doi: 10.1016/j.cllc.2020.02.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

295-307

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Patrick M Forde (PM)

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University, Baltimore, MD.

Phil Bonomi (P)

Section of Medical Oncology, Rush Medical Center, Chicago, IL.

Alice Shaw (A)

Thoracic Cancer Program, Massachusetts General Hospital, Boston, MA.

Gideon M Blumenthal (GM)

FDA's Oncology Center of Excellence, United Stated Food and Drug Administration, Silver Spring, MD.

Andrea Ferris (A)

LUNGevity Foundation, Bethesda, MD.

Chirag Patel (C)

FDA's Oncology Center of Excellence, United Stated Food and Drug Administration, Silver Spring, MD.

Allen Melemed (A)

Clinical Research Department, Eli-Lilly and Company, Indianapolis, IN.

Upal Basu Roy (U)

LUNGevity Foundation, Bethesda, MD.

Anuradha Ramamoorthy (A)

Office of Clinical Pharmacology, United Stated Food and Drug Administration, Silver Spring, MD.

Qi Liu (Q)

Office of Clinical Pharmacology, United Stated Food and Drug Administration, Silver Spring, MD.

Timothy Burns (T)

Division of Hematology/ Oncology, Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, PA.

Justin F Gainor (JF)

Thoracic Cancer Program, Massachusetts General Hospital, Boston, MA.

Christine Lovly (C)

Department of Medicine, Division of Hematology and Oncology, Vanderbilt University, Nashville, TN.

Zofia Piotrowska (Z)

Thoracic Cancer Program, Massachusetts General Hospital, Boston, MA.

Jonathan Lehman (J)

Department of Medicine, Division of Hematology and Oncology, Vanderbilt University, Nashville, TN.

Wendy Selig (W)

WSCollaborative, McLean, VA. Electronic address: wendy@wscollaborative.com.

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