Bendamustine as lymphodepletion for brexucabtagene autoleucel therapy of mantle cell lymphoma.

CAR T cells CAR-T MCL bendamustine brexucabtagene autoleucel mantle cell lymphoma

Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
15 Mar 2024
Historique:
received: 11 01 2024
revised: 29 02 2024
accepted: 12 03 2024
medline: 18 3 2024
pubmed: 18 3 2024
entrez: 17 3 2024
Statut: aheadofprint

Résumé

Brexucabtagene autoleucel (brexu-cel) is an autologous CD19-directed chimeric antigen receptor (CAR) T-cell therapy approved for treatment of relapsed/refractory mantle cell lymphoma (MCL). During a fludarabine shortage, we used bendamustine as an alternative to standard cyclophosphamide/fludarabine (cy/flu) lymphodepletion (LD) prior to brexu-cel. We assessed MCL patient outcomes as well as CAR T-cell expansion and persistence after brexu-cel following bendamustine or cy/flu LD at our center. This was a retrospective single institution study that utilized prospectively banked blood and tissue samples. Clinical efficacy was assessed by 2014 Lugano guidelines. CAR T-cell expansion and persistence in peripheral blood were assessed on day 7 and at ≥month 6 for patients with available samples. Seventeen patients received bendamustine and 5 received cy/flu. For the bendamustine cohort, 14 (82%) received bridging therapy and 4 (24%) had CNS involvement. Fifteen patients (88%) developed CRS with 4 (24%) ≥grade 3 events. Six (35%) patients developed ICANS with 4 (24%) events ≥grade 3. No patient had ≥grade 3 cytopenias at day 90. Best objective (BOR) and complete response (CRR) rates were 82% and 65%, respectively. At 24.5 months median follow-up, 12-month progression-free survival (PFS) was 45%, 24-month PFS was 25%, and median duration of response was 19 months. Median OS was not reached. BOR was 25% (1/4) for patients with CNS involvement. CAR transgene expansion after bendamustine LD was observed on day 7 in all (4/4) patients tested and persisted at ≥6 months (2/2), regardless of response. Bendamustine LD before brexu-cel for MCL is feasible and safe with a lower frequency and shorter duration of cytopenias than reported for cy/flu. Both CAR T-cell expansion and persistence were observed after bendamustine LD. Outcomes appear comparable to the real world outcomes reported with cy/flu LD.

Sections du résumé

BACKGROUND BACKGROUND
Brexucabtagene autoleucel (brexu-cel) is an autologous CD19-directed chimeric antigen receptor (CAR) T-cell therapy approved for treatment of relapsed/refractory mantle cell lymphoma (MCL). During a fludarabine shortage, we used bendamustine as an alternative to standard cyclophosphamide/fludarabine (cy/flu) lymphodepletion (LD) prior to brexu-cel.
OBJECTIVES OBJECTIVE
We assessed MCL patient outcomes as well as CAR T-cell expansion and persistence after brexu-cel following bendamustine or cy/flu LD at our center.
STUDY DESIGN METHODS
This was a retrospective single institution study that utilized prospectively banked blood and tissue samples. Clinical efficacy was assessed by 2014 Lugano guidelines. CAR T-cell expansion and persistence in peripheral blood were assessed on day 7 and at ≥month 6 for patients with available samples.
RESULTS RESULTS
Seventeen patients received bendamustine and 5 received cy/flu. For the bendamustine cohort, 14 (82%) received bridging therapy and 4 (24%) had CNS involvement. Fifteen patients (88%) developed CRS with 4 (24%) ≥grade 3 events. Six (35%) patients developed ICANS with 4 (24%) events ≥grade 3. No patient had ≥grade 3 cytopenias at day 90. Best objective (BOR) and complete response (CRR) rates were 82% and 65%, respectively. At 24.5 months median follow-up, 12-month progression-free survival (PFS) was 45%, 24-month PFS was 25%, and median duration of response was 19 months. Median OS was not reached. BOR was 25% (1/4) for patients with CNS involvement. CAR transgene expansion after bendamustine LD was observed on day 7 in all (4/4) patients tested and persisted at ≥6 months (2/2), regardless of response.
CONCLUSIONS CONCLUSIONS
Bendamustine LD before brexu-cel for MCL is feasible and safe with a lower frequency and shorter duration of cytopenias than reported for cy/flu. Both CAR T-cell expansion and persistence were observed after bendamustine LD. Outcomes appear comparable to the real world outcomes reported with cy/flu LD.

Identifiants

pubmed: 38494076
pii: S2666-6367(24)00288-4
doi: 10.1016/j.jtct.2024.03.015
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Elise A Chong (EA)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania. Electronic address: Elise.Chong@pennmedicine.upenn.edu.

Emeline R Chong (ER)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Dylan Therwhangher (D)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Sunita D Nasta (SD)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Daniel J Landsburg (DJ)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Stefan K Barta (SK)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Jakub Svoboda (J)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

James N Gerson (JN)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Guido Ghilardi (G)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Luca Paruzzo (L)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Joseph A Fraietta (JA)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Elizabeth Weber (E)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Natalie Stefano (N)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

David L Porter (DL)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Noelle V Frey (NV)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Alfred L Garfall (AL)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Marco Ruella (M)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Stephen J Schuster (SJ)

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania.

Classifications MeSH