Outcomes of first therapy after CD19-CAR-T treatment failure in large B-cell lymphoma

© 2022. The Author(s), under exclusive licence to Springer Nature Limited..

Persistence or recurrence of large B-cell lymphoma after CD19-CAR-T is common, yet data guiding management are limited. We describe outcomes and features following CAR-T treatment failure. Of 305 adults who received CD19-CAR-T, 182 experienced disease recurrence or progression (1-year cumulative incidence 63% [95%CI: 57-69]). Of 52 post-CAR-T biopsies evaluated by flow cytometry, 49 (94%) expressed CD19. Subsequent anti-cancer treatment was administered in 135/182 (74%) patients with CAR-T treatment failure. Median OS from the first post-CAR-T treatment was 8 months (95%CI 5.6-11.0). Polatuzumab-, standard chemotherapy-, and lenalidomide-based treatments were the most common approaches after CAR-T. No complete responses (CRs) were observed with conventional chemotherapy, while CR rates exceeding 30% were seen following polatuzumab- or lenalidomide-based therapies. Factors associated with poor OS among patients treated post-CAR-T were pre-CAR-T bulky disease (HR 2.27 [1.10-4.72]), lack of response to CAR-T (2.33 [1.02-5.29]), age >65 years (HR 2.65 [1.49-4.73]) and elevated LDH at post-CAR-T treatment (HR 2.95 [1.61-5.38]). The presence of ≥2 of these factors was associated with inferior OS compared to ≤1 (56% vs. 19%). In this largest analysis to date of patients who progressed or relapsed after CD19-CAR-T, survival is poor, though novel agents such as polatuzumab and lenalidomide may have hold promise.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:37

Enthalten in:

Leukemia - 37(2023), 1 vom: 05. Jan., Seite 154-163

Sprache:

Englisch

Beteiligte Personen:

Alarcon Tomas, Ana [VerfasserIn]
Fein, Joshua A [VerfasserIn]
Fried, Shalev [VerfasserIn]
Flynn, Jessica R [VerfasserIn]
Devlin, Sean M [VerfasserIn]
Fingrut, Warren B [VerfasserIn]
Anagnostou, Theodora [VerfasserIn]
Alperovich, Anna [VerfasserIn]
Shah, Nishi [VerfasserIn]
Fraint, Ellen [VerfasserIn]
Lin, Richard J [VerfasserIn]
Scordo, Michael [VerfasserIn]
Batlevi, Connie Lee [VerfasserIn]
Besser, Michal J [VerfasserIn]
Dahi, Parastoo B [VerfasserIn]
Danylesko, Ivetta [VerfasserIn]
Giralt, Sergio [VerfasserIn]
Imber, Brandon S [VerfasserIn]
Jacoby, Elad [VerfasserIn]
Kedmi, Meirav [VerfasserIn]
Nagler, Arnon [VerfasserIn]
Palomba, M Lia [VerfasserIn]
Roshal, Mikhail [VerfasserIn]
Salles, Gilles A [VerfasserIn]
Sauter, Craig [VerfasserIn]
Shem-Tov, Noga [VerfasserIn]
Shimoni, Avichai [VerfasserIn]
Yahalom, Joachim [VerfasserIn]
Yerushalmi, Ronit [VerfasserIn]
Shah, Gunjan L [VerfasserIn]
Avigdor, Abraham [VerfasserIn]
Perales, Miguel-Angel [VerfasserIn]
Shouval, Roni [VerfasserIn]

Links:

Volltext

Themen:

Antigens, CD19
F0P408N6V4
Journal Article
Lenalidomide
Receptors, Chimeric Antigen
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 31.01.2023

Date Revised 03.07.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1038/s41375-022-01739-2

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM34849131X