Benefit of axicabtagene ciloleucel versus chemoimmunotherapy in older patients and/or patients with poor ECOG performance status with relapsed or refractory large B‐cell lymphoma after 2 or more lines of prior therapy

Author:

Lunning Matthew A.1ORCID,Wang Hai‐lin2,Hu Zhen‐Huan2,Locke Frederick L.3,Siddiqi Tanya4,Jacobson Caron A.5,Ahmed Sairah6,Miklos David B.7,Lin Yi8,Hill Brian T.9,Ghobadi Armin10,Neelapu Sattva S.6,Westin Jason6ORCID,Dieyi Chrisopher2,Field Polly11,Miao Harry2,Shahani Shilpa A.2,Patel Anik2,Spooner Clare2,Fu Christine2,Muramoto David2,Xu Hairong2,Pasquini Marcelo C.12

Affiliation:

1. University of Nebraska Omaha Nebraska USA

2. Kite, A Gilead Company Santa Monica California USA

3. Moffitt Cancer Center Tampa Florida USA

4. City of Hope National Medical Center Duarte California USA

5. Dana‐Farber Cancer Institute Boston Massachusetts USA

6. The University of Texas MD Anderson Cancer Center Houston Texas USA

7. Stanford University School of Medicine Stanford California USA

8. Mayo Clinic Rochester Minnesota USA

9. Cleveland Clinic Foundation Cleveland Ohio USA

10. Washington University School of Medicine St Louis Missouri USA

11. Oxford PharmaGenesis Oxford UK

12. CIBMTR Milwaukee Wisconsin USA

Abstract

AbstractAxicabtagene ciloleucel (axi‐cel) in trials has demonstrated favorable efficacy compared with historical controls after ≥2 lines of therapy for the treatment of relapsed or refractory (R/R) large B cell lymphoma (LBCL). Herein, we compared the real‐world effectiveness of axi‐cel with efficacy and effectiveness of chemoimmunotherapy (CIT) in patients aged ≥65 years and patients with Eastern Cooperative Oncology Group performance status (ECOG PS) of 2. A total of 1146 patients treated with commercial axi‐cel for R/R LBCL with ≥2 lines of prior therapy were included from the Center for International Blood and Marrow Transplantation Research prospective observational study, and 469 patients treated with CIT for R/R LBCL after ≥2 lines of prior therapy were included from SCHOLAR‐1 (an international, multicohort, retrospective study). After propensity score matching, at a median follow‐up of 24 months for patients receiving axi‐cel and 60 months for patients receiving CIT, 12‐month overall survival rates were 62% and 28%, respectively (hazard ratio, 0.30 [95% CI, 0.24–0.37]). Objective response rate (ORR) was 76% (complete response [CR] rate 58%) in patients receiving axi‐cel versus 28% (CR rate 16%) for those receiving CIT. A 57% difference in ORR (55% difference in CR rate) favoring axi‐cel over CIT was observed among patients aged ≥65 years. Increased magnitude of benefit in response rates for axi‐cel versus CIT was also observed among patients with ECOG PS = 2. These findings further support the broader use of axi‐cel in older patients and patients with ECOG PS = 2 with R/R LBCL.

Funder

National Institute of Allergy and Infectious Diseases

National Heart, Lung, and Blood Institute

National Cancer Institute

Health Resources and Services Administration

Office of Naval Research

Publisher

Wiley

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