Evaluating Lab-Based Eligibility Criteria by Race/Ethnicity in Clinical Trials of Diffuse Large B-Cell Lymphoma.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
11 Jul 2024
Historique:
accepted: 30 06 2024
received: 02 02 2024
revised: 28 06 2024
medline: 11 7 2024
pubmed: 11 7 2024
entrez: 11 7 2024
Statut: aheadofprint

Résumé

Underrepresentation of racial and ethnic subgroups in cancer clinical trials remains a persistent challenge. Restrictive clinical trial eligibility criteria have been shown to exacerbate this problem. We previously identified that up to 24% of patients treated with standard immunochemotherapy (IC) would have been excluded from recent first-line trials in diffuse large B-cell lymphoma (DLBCL) based on 5 lab-based criteria. These ineligible patients had worse clinical outcomes and increased deaths related to lymphoma progression suggesting the potential exclusion of patients who could have benefited most from the novel therapies being evaluated. Utilizing data from the prospectively enrolled Lymphoma Epidemiology Outcomes (LEO) Cohort study, with demographics broadly similar to the U.S. patients diagnosed with lymphoma, we evaluated the impact of laboratory eligibility criteria from recent first-line DLBCL trials across various racial and ethnic backgrounds. There were significant differences in the baseline lab values by race/ethnicity with Black/African American (AA) patients having the lowest mean hemoglobin and highest creatinine clearance. Based on recent clinical trial eligibility criteria, AA and Hispanic patients had higher rates of lab-based ineligibility compared to Non-Hispanic Whites. The largest gap in the clinical outcomes between eligible (ref) and non-eligible patients was noted within AA patients with an overall survival hazard ratio based on POLARIX clinical trial criteria of 4.09, 95% CI: 1.83-9.14. A thoughtful approach to the utility of each criterion and cut offs for eligibility needs to be evaluated in the context of its differential impact across various racial/ethnic groups.

Identifiants

pubmed: 38991126
pii: 516945
doi: 10.1182/bloodadvances.2024012838
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Arushi Khurana (A)

Mayo Clinic, Rochester, Minnesota, United States.

Raphael Mwangi (R)

Mayo Clinic, Rochester, Minnesota, United States.

Loretta J Nastoupil (LJ)

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Patrick M Reagan (PM)

University of Rochester Medical Center, Rochester, New York, United States.

Umar Farooq (U)

University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States.

Jason T Romancik (JT)

Emory University, Atlanta, Georgia, United States.

Timothy McDonnell (T)

MD Anderson Cancer Center, Houston, Texas, United States.

Shaun Riska (S)

Mayo Clinic, Rohcester, Minnesota, United States.

Izidore S Lossos (IS)

University of Miami, Miami, Florida, United States.

Brad S Kahl (BS)

Washington University in St Louis, St Louis, Missouri, United States.

Peter Martin (P)

Weill Cornell Medical College, New York, New York, United States.

Thomas E Witzig (TE)

Mayo Clinic, Rochester, Minnesota, United States.

James R Cerhan (JR)

Mayo Clinic College of Medicine, Rochester, Minnesota, United States.

Christopher R Flowers (CR)

UT MD Anderson Cancer Center, Houston, Texas, United States.

Grzegorz S Nowakowski (GS)

Mayo Clinic, Rochester, Minnesota, United States.

Matthew J Maurer (MJ)

Mayo Clinic, Rochester, Minnesota, United States.

Classifications MeSH