Conditioning regimens for allotransplants for diffuse large B-cell lymphoma: myeloablative or reduced intensity?

Author:

Bacher Ulrike12,Klyuchnikov Evgeny1,Le-Rademacher Jennifer3,Carreras Jeanette3,Armand Philippe4,Bishop Michael R.5,Bredeson Christopher N.6,Cairo Mitchell S.7,Fenske Timothy S.8,Freytes Cesar O.9,Gale Robert Peter10,Gibson John11,Isola Luis M.12,Inwards David J.13,Laport Ginna G.14,Lazarus Hillard M.15,Maziarz Richard T.16,Wiernik Peter H.17,Schouten Harry C.18,Slavin Shimon19,Smith Sonali M.20,Vose Julie M.21,Waller Edmund K.22,Hari Parameswaran N.3

Affiliation:

1. Department for Stem Cell Transplantation, University of Hamburg, Hamburg, Germany;

2. MLL Munich Leukemia Laboratory, Munich, Germany;

3. Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;

4. Dana-Farber Cancer Institute, Boston, MA;

5. Medical College of Wisconsin, Milwaukee, WI;

6. Ottawa Hospital Blood & Marrow Transplant Program, Ottawa, ON;

7. New York Medical College, Valhalla, NY;

8. Froedtert Memorial Lutheran Hospital, Milwaukee, WI;

9. South Veterans Health Care System and University of Texas Health Science Center, San Antonio, TX;

10. Imperial College, London, United Kingdom;

11. Royal Prince Alfred Hospital Institute of Haematology, Camperdown, Australia;

12. Mount Sinai Medical Center, New York, NY;

13. Mayo Clinic, Rochester, MN;

14. Stanford Hospital and Clinics, Stanford, CA;

15. University Hospital Case Medical Center, Cleveland, OH;

16. Oregon Health and Science University, Portland, OR;

17. New York Medical College, Bronx, NY;

18. Academische Ziekenhuis Maastricht, Maastricht, The Netherlands;

19. International Center for Cell Therapy & Cancer Immunotherapy, Tel Aviv, Israel;

20. University of Chicago Hospitals, Chicago, IL;

21. Nebraska Medical Center, Omaha, NE; and

22. Emory University Hospital, Atlanta, GA

Abstract

Abstract The best conditioning regimen before allogeneic transplantation for high-risk diffuse large B-cell lymphoma (DLBCL) remains to be clarified. We analyzed data from 396 recipients of allotransplants for DLBCL receiving myeloablative (MAC; n = 165), reduced intensity (RIC; n = 143), or nonmyeloablative conditioning (NMAC; n = 88) regimens. Acute and chronic GVHD rates were similar across the groups. Five-year nonrelapse mortality (NRM) was higher in MAC than RIC and NMAC (56% vs 47% vs 36%; P = .007). Five-year relapse/progression was lower in MAC than in RIC/NMAC (26% vs 38% vs 40%; P = .031). Five-year progression-free survival (15%-25%) and overall survival (18%-26%) did not differ significantly between the cohorts. In multivariate analysis, NMAC and more recent transplant year were associated with lower NRM, whereas a lower Karnofsky performance score (< 90), prior relapse resistant to therapy, and use of unrelated donors were associated with higher NRM. NMAC transplants, no prior use of rituximab, and prior relapse resistant to therapy were associated with a greater risk of relapse/progression. In conclusion, allotransplantation with RIC or NMAC induces long-term progression-free survival in selected DLBCL patients with a lower risk of NRM but with higher risk of lymphoma progression or relapse.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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