PD-1 blockade for diffuse large B-cell lymphoma after autologous stem cell transplantation

Author:

Frigault Matthew J.1ORCID,Armand Philippe2,Redd Robert A.3ORCID,Jeter Erin2,Merryman Reid W.2,Coleman Kimberly C.2,Herrera Alex F.4,Dahi Parastoo5,Nieto Yago6ORCID,LaCasce Ann S.2ORCID,Fisher David C.2,Ng Samuel Y.2,Odejide Oreife O.2,Freedman Arnold S.2,Kim Austin I.2,Crombie Jennifer L.2,Jacobson Caron A.2,Jacobsen Eric D.2,Wong Jeffrey L.2,Bsat Jad2,Patel Sanjay S.7,Ritz Jerome2ORCID,Rodig Scott J.7,Shipp Margaret A.2ORCID,Chen Yi-Bin1,Joyce Robin M.8ORCID

Affiliation:

1. Blood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA;

2. Department of Medical Oncology and

3. Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA;

4. Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA;

5. Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY;

6. Department of Stem Cell Transplantation & Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX;

7. Department of Pathology, Brigham and Women’s Hospital, Boston, MA; and

8. Department of Hematology and Oncology, Beth Israel Deaconess Medical Center, Boston, MA

Abstract

Abstract Disease relapse remains the leading cause of failure after autologous stem cell transplantation (ASCT) for patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). We conducted a phase 2, multicenter, single-arm study of the anti–PD-1 monoclonal antibody pembrolizumab given after ASCT in patients with chemosensitive DLBCL, hypothesizing that it would improve the progression-free survival (PFS) at 18 months after ASCT (primary endpoint) from 60% to 80%. Pembrolizumab was administered at 200 mg IV every 3 weeks for up to 8 cycles, starting within 21 days of post-ASCT discharge. Twenty-nine patients were treated on this study; 62% completed all 8 cycles. Seventy-nine percent of patients experienced at least one grade 3 or higher adverse event, and 34% experienced at least one grade 2 or higher immune-related adverse event. Overall, 59% of patients were alive and progression free at 18 months, which did not meet the primary endpoint. The 18-month overall survival was 93%. In conclusion, pembrolizumab was successfully administered as post-ASCT consolidation in patients with R/R DLBCL, but the PFS did not meet the protocol-specific primary objective and therefore does not support a larger confirmatory study. This trial was registered at www.clinicaltrials.gov as #NCT02362997.

Publisher

American Society of Hematology

Subject

Hematology

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