Abstract
The antibody-drug conjugate polatuzumab vedotin (pola) has recently been approved in combination with bendamustine and rituximab (pola-BR) for patients with refractory or relapsed (r/r) large B-cell lymphoma (LBCL). To investigate the efficacy of pola-BR in a real-world setting, we retrospectively analyzed 105 patients with LBCL who were treated in 26 German centers under the national compassionate use program. Fifty-four patients received pola as a salvage treatment and 51 patients were treated with pola with the intention to bridge to chimeric antigen receptor (CAR) T-cell therapy (n 5 41) or allogeneic hematopoietic cell transplantation (n = 10). Notably, patients in the salvage and bridging cohort had received a median of 3 prior treatment lines. In the salvage cohort, the best overall response rate was 48.1%. The 6-month progression-free survival and overall survival (OS) was 27.7% and 49.6%, respectively. In the bridging cohort, 51.2% of patients could be successfully bridged with pola to the intended CAR T-cell therapy. The combination of pola bridging and successful CAR T-cell therapy resulted in a 6-month OS of 77.9% calculated from pola initiation. Pola vedotin-rituximab without a chemotherapy backbone demonstrated encouraging overall response rates up to 40%, highlighting both an appropriate alternative for patients unsuitable for chemotherapy and a new treatment option for bridging before leukapheresis in patients intended for CAR T-cell therapy. Furthermore, 7 of 12 patients with previous failure of CAR T-cell therapy responded to a pola-containing regimen. These findings suggest that pola may serve as effective salvage and bridging treatment of r/r LBCL patients.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Blood Advances |
| Jahrgang | 5 |
| Ausgabenummer | 13 |
| Seiten (von - bis) | 2707-2716 |
| Seitenumfang | 10 |
| ISSN | 2473-9529 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 13.07.2021 |
Fördermittel
N.L. was supported by the Heidelberg School of Oncology (HSO2) fellowship from the National Center for Tumor Diseases Heidelberg. S.D. was supported by a grant from the Hairy Cell Leukemia Foundation, Heidelberg Research Centre for Molecular Medicine, an e:med BMBF junior group grant, and Deutsche Forschungsgemeinschaft (DFG) through the SFB873 (project B7). Conflict-of-interest disclosure: N.L. reports honoraria from Takeda and Roche. J.D. reports research funding from Morphosys and This study was not financially supported by F. Hoffmann-La Roche or Genentech.
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
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