CD19-directed CART Therapy for T cell/Histiocyte Rich 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:
10 Jul 2024
Historique:
accepted: 26 06 2024
received: 04 06 2024
revised: 24 06 2024
medline: 10 7 2024
pubmed: 10 7 2024
entrez: 10 7 2024
Statut: aheadofprint

Résumé

T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) is a rare histologic variant of LBCL. Limited data regarding CD19-directed chimeric antigen receptor T-cell (CART) therapy in relapsed/refractory (R/R) THRLBCL suggest poor efficacy. We investigated CART outcomes for R/R THRLBCL through the CIBMTR registry. A total of 58 adult patients with R/R THRLBCL who received commercial CD19-CART between 2018-2022 were identified. Most patients (67%) had early relapse of disease (45% primary refractory) with a median of 3 (range: 1-7) prior therapies and were treated with Axicabtagene ciloleucel (69%). At median follow-up of 23 months post-CART, 2-year overall and progression-free survival were 42% (95% CI: 27-57) and 29% (95% CI: 17-43), respectively. In univariable analysis, poor performance status pre-CART was associated with higher mortality (HR 2.35, 95%CI 1.02-5.5). The 2-year cumulative incidences of relapse/progression and non-relapse mortality were 69% and 2%, respectively. Grade ≥3 CRS and ICANS occurred in 7% and 15% of patients, respectively. In this largest analysis of CD19-CART for R/R THRLBCL, approximately 30% of patients were alive and progression-free 2 years post-CART. Despite a high incidence of progression (69% at 2 years), these results suggest a subset of patients with R/R THRLBCL may have durable responses with CART.

Identifiants

pubmed: 38985302
pii: 516930
doi: 10.1182/bloodadvances.2024013863
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Priyanka A Pophali (PA)

University of Wisconsin Carbone Cancer Center, Madison, Wisconsin, United States.

Joshua A Fein (JA)

Weill Cornell Medicine/NewYork Presbyterian Hospital, New York, New York, United States.

Kwang Woo Ahn (KW)

Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Molly Allbee-Johnson (M)

Medical College of Wisconsin, Milwaukee, Wisconsin, United States.

Nausheen Ahmed (N)

University of Kansas Cancer Center, Westwood, Kansas, United States.

Farrukh T Awan (FT)

UT Southwestern, Dallas, Texas, United States.

Shatha Farhan (S)

Henry Ford Healthsystem, detroit, Michigan, United States.

Natalie S Grover (NS)

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, United States.

Talal Hilal (T)

Mayo Clinic, Phoenix, Arizona, United States.

Madiha Iqbal (M)

Mayo Clinic Florida, Jacksonville, Florida, United States.

Joeseph Maakaron (J)

University of Minnesota, Minneapolis, Minnesota, United States.

Dipenkumar Modi (D)

Barbara Ann Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, United States.

Elham Nasrollahi (E)

University of Pittsburgh Medical Center in Central PA, Harrisburg, Pennsylvania, United States.

Levanto Schachter (L)

University of California Los Angeles, San Luis Obispo, California, United States.

Craig S Sauter (CS)

Cleveland Clinic, Cleveland, Ohio, United States.

Mehdi Hamadani (M)

Medical College of Wisconsin, Wauwatosa, Wisconsin, United States.

Alex F Herrera (AF)

City of Hope, Duarte, California, United States.

Roni Shouval (R)

Memorial Sloan Kettering Cancer Center, New York, New York, United States.

Mazyar Shadman (M)

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States.

Classifications MeSH