Outcomes of subsequent antilymphoma therapies after second-line axicabtagene ciloleucel or standard of care in ZUMA-7

Author:

Ghobadi Armin1ORCID,Munoz Javier2,Westin Jason R.3ORCID,Locke Frederick L.4,Miklos David B.5ORCID,Rapoport Aaron P.6,Perales Miguel-Angel7ORCID,Reagan Patrick M.8,McGuirk Joseph9ORCID,Jacobson Caron A.10,Kersten Marie José11,Avivi Irit12,Peng Andrew13,Schupp Marco13,To Christina13,Oluwole Olalekan O.14ORCID

Affiliation:

1. 1Department of Medicine, Division of Medical Oncology, Washington University School of Medicine, St Louis, MO

2. 2Banner MD Anderson Cancer Center, Gilbert, AZ

3. 3Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

4. 4Department of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL

5. 5Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University School of Medicine, Stanford, CA

6. 6Department of Medicine, University of Maryland School of Medicine and Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD

7. 7Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

8. 8Wilmot Cancer Institute, University of Rochester School of Medicine, Rochester, NY

9. 9Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Cancer Center, Kansas City, KS

10. 10Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

11. 11Amsterdam UMC, Location University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands

12. 12Department of Hematology, Tel Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

13. 13Kite, a Gilead company, Santa Monica, CA

14. 14Division of Hematology Oncology, Department of Medicine, Vanderbilt University Cancer Center, Nashville, TN

Abstract

Abstract The optimal management of patients with relapsed/refractory large B-cell lymphoma (LBCL) after disease progression or lack of response to second-line (2L) therapy remains unclear. Here, we report outcomes among patients who received subsequent antilymphoma therapy per investigator discretion separately by their randomized 2L arm in ZUMA-7, namely axicabtagene ciloleucel (axi-cel) vs standard of care (SOC). Progression-free survival (PFS) and overall survival (OS) were calculated from 3L therapy initiation. In the SOC arm, 127 of 179 randomized patients (71%) received 3L therapy. Median PFS among those who received 3L cellular immunotherapy (n = 68) vs those who did not (n = 59) was 6.3 vs 1.9 months, respectively; median OS was 16.3 vs 9.5 months, respectively. In the axi-cel arm, 84 of 180 randomized patients (47%) received 3L therapy. Median PFS among those who received 3L chemotherapy (n = 60) vs cellular immunotherapy (n = 8) was 1.7 vs 3.5 months, respectively; median OS was 8.1 months vs not reached, respectively. Of the 60 patients who received 3L chemotherapy, 10 underwent stem cell transplantation (SCT) after salvage chemotherapy. Median PFS was 11.5 vs 1.6 months, and median OS was 17.5 vs 7.2 months for those who did vs did not reach SCT, respectively. Eight patients received 3L cellular immunotherapy after 2L axi-cel. Of these, 6 patients received subsequent SCT in any line; all 6 were alive at data cutoff. These findings help inform subsequent treatment choices after 2L therapy failure for relapsed/refractory LBCL. The trial was registered at www.clinicaltrials.gov as #NCT03391466.

Publisher

American Society of Hematology

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