Outcomes of allogeneic hematopoietic stem cell transplantation for relapsed or refractory diffuse large B-cell lymphoma

Author:

Kato Koji1,Sugio Takeshi2,Ikeda Takashi3ORCID,Yoshitsugu Kanako3,Miyzaki Kana4,Suzumiya Junji5,Yamamoto Go6,Kim Sung-Won7,Ikegame Kazuhiro8ORCID,Uehara Yasufumi9,Mori Yasuo10ORCID,Ishikawa Jun11,Hiramoto Nobuhiro12,Eto Tetsuya13,Nakazawa Hideyuki14,Kobayashi Hikaru15,Serizawa Kentaro16,Onizuka Makoto17ORCID,Fukuda Takahiro7,Atsuta Yoshiko18ORCID,Suzuki Ritsuro19ORCID

Affiliation:

1. Kyushu University Graduate School of Medical Science

2. Stanford University

3. Shizuoka Cancer Center

4. Mie University Graduate School of Medicine

5. Shimane University Hospital

6. Toranomon Hospital

7. National Cancer Center Hospital

8. Hyogo College of Medicine Hospital

9. Kitakyushu City Hospital Organization Kitakyushu Municipal Medical Center

10. Kyushu University Hospital

11. Osaka International Cancer Institute

12. Kobe City Medical Center General Hospital

13. Hamanomachi Hospital

14. Shinshu University School of Medicine

15. Nagano Red Cross Hospital

16. Kindai University Hospital

17. Tokai University School of Medicine

18. Japanese Data Center for Hematopoietic Cell Transplantation/Nagoya University Graduate School of Medicine

19. Shimane University

Abstract

Abstract Allogeneic hematopoietic stem cell transplantation (allo-HSCT) are curative treatment modalities for diffuse large B-cell lymphoma (DLBCL) because of the intrinsic graft-versus-lymphoma effect. However, limited information is available regarding which patients with relapsed or refractory DLBCL are likely to benefit from allo-HSCT. We retrospectively analyzed data from 1,268 DLBCL patients who received allo-HSCT. The overall survival and progression-free survival (PFS) rates were 30.3% and 21.6% at 3 years, respectively. Multivariate analysis revealed that stable or progressive disease at transplantation, male patient, poorer performance status at transplantation and shorter interval from previous transplantation were associated independently with a lower PFS. Four prognostic factors were used to construct a prognostic index for PFS, predicting 3-year PFS of 55.4%, 43.7%, 20.4% and 6.6%, respectively. The prognostic model predicted relapse rates following allo-HSCT accordingly (P < 0.0001), whereas did not predict transplantation-related mortality (P = 0.249). The prognostic index can identify a subgroup of DLBCL patients whobenefit from allo-HSCT and it is worthwhile to evaluate whether this model is also applicable to patients undergoing allo-HSCT in cases of relapse after chimeric antigen receptor engineered T-cell therapy, although the application of allo-HSCT has been declining with the increase of novel immunotherapies.

Publisher

Research Square Platform LLC

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