Axicabtagene ciloleucel versus standard of care in second-line large B-cell lymphoma: outcomes by metabolic tumor volume.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
01 Apr 2024
Historique:
accepted: 06 03 2024
received: 26 06 2023
revised: 15 02 2024
medline: 1 4 2024
pubmed: 1 4 2024
entrez: 1 4 2024
Statut: aheadofprint

Résumé

Metabolic tumor volume (MTV) assessed using 2-deoxy-2-[18F]fluoro-D-glucose positron emission tomography, a measure of tumor burden, is a promising prognostic indicator in large B-cell lymphoma (LBCL). This exploratory analysis evaluated relationships between baseline MTV (categorized as low [≤median] vs high [>median]) and clinical outcomes in the phase 3 ZUMA-7 study (NCT03391466). Patients with LBCL relapsed within 12 months of or refractory to first-line chemoimmunotherapy were randomized 1:1 to axicabtagene ciloleucel (axi-cel; autologous anti-CD19 chimeric antigen receptor [CAR] T-cell therapy) or standard care (2-3 cycles of chemoimmunotherapy followed by high-dose chemotherapy with autologous stem-cell transplantation in patients who had a response). All P values are descriptive. Within high and low MTV subgroups, event-free survival (EFS) and progression-free survival (PFS) were superior with axi-cel vs standard care (all HR ≤0.523; P<.01). EFS in patients with high MTV (vs low MTV) was numerically shorter with axi-cel (HR, 1.448; P=.06) and was significantly shorter with standard care (HR, 1.486; P=.02). PFS was shorter in patients with high MTV vs low MTV in both the axi-cel (HR,1.660; P=.02) and standard-care (HR, 1.635; P=.02) arms, and median MTV was lower in patients in ongoing response at data cutoff vs others (both P≤.01). Median MTV was higher in axi-cel-treated patients who experienced grade ≥3 neurologic events or cytokine release syndrome (CRS) than in patients with grade 1/2 or no neurologic events or CRS, respectively (both P≤.03). Baseline MTV ≤median was associated with better clinical outcomes in patients receiving axi-cel or standard care for second-line LBCL.

Identifiants

pubmed: 38557775
pii: 515553
doi: 10.1182/blood.2023021620
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Frederick L Locke (FL)

Moffitt Cancer Center, Tampa, Florida, United States.

Olalekan O Oluwole (OO)

Vanderbilt University Medical Center, Nashville, Tennessee, United States.

John Kuruvilla (J)

Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Catherine Thieblemont (C)

AP-HP, Hôpital Saint-Louis, Hemato-oncologie, DMU DHI,F-75010 Paris, France, Paris, France.

Franck Morschhauser (F)

University of Lille, Lille, France.

Gilles A Salles (GA)

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

Steven P Rowe (SP)

University of North Carolina, Chapel Hill, Chapel Hill, North Carolina, United States.

Saran Vardhanabhuti (S)

Kite, a Gilead Company, Santa Monica, California, United States.

Joshua Winters (J)

Kite, a Gilead Company, Santa Monica, California, United States.

Simone Filosto (S)

Kite, a Gilead Company, Santa Monica, California, United States.

Christina To (C)

Kite, A Gilead Company, Santa Monica, California, United States.

Paul Cheng (P)

Kite, Santa Monica, California, United States.

Marco Schupp (M)

Kite, a Gilead Company, Santa Monica, California, United States.

Ronald Korn (R)

Imaging Endpoints, Scottsdale, Arizona, United States.

Marie José Kersten (MJ)

Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.

Classifications MeSH