Autologous stem cell transplantation after anti-PD-1 therapy for multiply relapsed or refractory Hodgkin lymphoma

Author:

Merryman Reid W.1,Redd Robert A.2ORCID,Nishihori Taiga3ORCID,Chavez Julio3,Nieto Yago4ORCID,Darrah Justin M.56,Rao Uttam7,Byrne Michael T.7,Bond David A.8ORCID,Maddocks Kami J.8,Spinner Michael A.9,Advani Ranjana H.9,Ballard Hatcher J.10,Svoboda Jakub10,Singh Anurag K.11,McGuirk Joseph P.11ORCID,Modi Dipenkumar12ORCID,Ramchandren Radhakrishnan13,Romancik Jason14ORCID,Cohen Jonathon B.14ORCID,Frigault Matthew J.15,Chen Yi-Bin15,Serritella Anthony V.16,Kline Justine16,Ansell Stephen17,Nathan Sunita18,Rahimian Maryam19,Joyce Robin M.19ORCID,Shah Mansi20ORCID,David Kevin A.20,Park Steven21ORCID,Beaven Anne W.22,Habib Alma23,Bachanova Veronika23,Nakhoda Shazia24,Khan Nadia24,Lynch Ryan C.25ORCID,Smith Stephen D.25ORCID,Ho Vincent T.1,LaCasce Ann1ORCID,Armand Philippe1,Herrera Alex F.5

Affiliation:

1. Division of Hematologic Malignancies and

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

3. Department of Blood & Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL;

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

5. Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA;

6. Cedars-Sinai Medical Center, Los Angeles, CA;

7. Division of Hematology-Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN;

8. Division of Hematology, Department of Internal Medicine, Arthur G. James Comprehensive Cancer Center, The Ohio State University Hospital, Columbus, OH;

9. Division of Oncology, Department of Medicine, Stanford University, Stanford, CA;

10. Division of Hematology-Oncology, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA;

11. Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS;

12. Department of Oncology, Karmanos Cancer Institute/Wayne State University, Detroit, MI;

13. Division of Hematology/Oncology, University of Tennessee School of Medicine, Knoxville, TN;

14. Department of Hematology and Medical Oncology, Emory University–Winship Cancer Institute, Atlanta, GA;

15. Bone Marrow Transplantation Program, Massachusetts General Hospital, Boston, MA;

16. Section of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL;

17. Division of Hematology, Mayo Clinic, Rochester, MN;

18. Section of Bone Marrow Transplant and Cell Therapy, Rush University Medical Center, Chicago, IL;

19. Beth Israel Deaconess Medical Center, Boston, MA;

20. Rutgers Cancer Institute of New Jersey, New Brunswick, NJ;

21. Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Charlotte, NC;

22. Division of Hematology, University of North Carolina, Chapel Hill, NC;

23. Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN;

24. Division of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA; and

25. University of Washington/Fred Hutchinson Cancer Research Center, Seattle, WA

Abstract

Abstract Autologous stem cell transplantation (ASCT) can be curative for patients with relapsed/refractory Hodgkin lymphoma (HL). Based on studies suggesting that anti-PD-1 monoclonal antibodies (mAbs) can sensitize patients to subsequent chemotherapy, we hypothesized that anti-PD-1 therapy before ASCT would result in acceptable outcomes among high-risk patients who progressed on or responded insufficiently to ≥1 salvage regimen, including chemorefractory patients who are traditionally considered poor ASCT candidates. We retrospectively identified 78 HL patients who underwent ASCT after receiving an anti-PD-1 mAb (alone or in combination) as third-line or later therapy across 22 centers. Chemorefractory disease was common, including 42 patients (54%) refractory to ≥2 consecutive systemic therapies immediately before anti-PD-1 treatment. Fifty-eight (74%) patients underwent ASCT after anti-PD-1 treatment, while 20 patients (26%) received additional therapy after PD-1 blockade and before ASCT. Patients received a median of 4 systemic therapies (range, 3-7) before ASCT, and 31 patients (41%) had a positive pre-ASCT positron emission tomography (PET) result. After a median post-ASCT follow-up of 19.6 months, the 18-month progression-free survival (PFS) and overall survival were 81% (95% CI, 69-89) and 96% (95% confidence interval [CI], 87-99), respectively. Favorable outcomes were observed for patients who were refractory to 2 consecutive therapies immediately before PD-1 blockade (18-month PFS, 78%), had a positive pre-ASCT PET (18-month PFS, 75%), or received ≥4 systemic therapies before ASCT (18-month PFS, 73%), while PD-1 nonresponders had inferior outcomes (18-month PFS, 51%). In this high-risk cohort, ASCT after anti-PD-1 therapy was associated with excellent outcomes, even among heavily pretreated, previously chemorefractory patients.

Publisher

American Society of Hematology

Subject

Hematology

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