Impact of standard-dose dipeptidyl peptidase-4 inhibitors on the incidence of graft-versus-host disease among diabetes mellitus patients undergoing allogeneic hematopoietic cell transplantation: a KSGCT multicenter retrospective study

Author:

Kanda Yoshinobu1ORCID,Kimura Shun-ichi2ORCID,Shimizu Hiroaki3,Miyazaki Takuya4,Sakurai Masatoshi5ORCID,Tanoue Susumu6,Kayamori Kensuke7ORCID,Ohwada Chikako8ORCID,Yoshimura Kazuki9ORCID,Nakasone Hideki9ORCID,Ohashi Takuma10ORCID,Shono Katsuhiro11ORCID,Tachibana Takayoshi12ORCID,Hatano Kaoru13,Okada Keigo14,Kimura Yuta15,Seo Sachiko16,Doki Noriko17,Tanaka Masatsugu12,Hatta Yoshihiro18,Takahashi Satoshi19ORCID

Affiliation:

1. Division of Hematology, Department of Medicine, Jichi Medical University, Tochigi, Japan

2. Saitama Medical Center, Jichi Medical University

3. Tokyo Metropolitan Cancer and Infectious Diseases Center

4. Yokohama City University

5. Keio University School of Medicine

6. The Institute of Medical Science, The University of Tokyo

7. Department of Hematology, Chiba University Hospital

8. Chiba University Hospital

9. Jichi Medical University Saitama Medical Center

10. Yokohama City University Medical Center

11. Chiba Aoba Municipal Hospital

12. Kanagawa Cancer Center

13. Jichi Medical University

14. Tokyo Medical and Dental University

15. Saitama Medical Center, Saitama Medical University

16. Dokkyo Medical University

17. Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital

18. Nihon University School of Medicine

19. Institute of Medical Science, University Tokyo

Abstract

Abstract This study aimed to evaluate the impact of standard-dose dipeptidyl peptidase-4 inhibitors (DPP-4i) on the incidence of graft-versus-host disease (GVHD) after allogeneic hematopoietic cell transplantation (HCT). We retrospectively evaluated 207 diabetes mellitus patients undergoing allogeneic HCT between 2010 and 2019. The 100-day cumulative incidences (CI) of grade II–IV acute GVHD (aGVHD) in patients who took DPP-4i from day − 1 to 14, those who did not, and those who discontinued DPP-4i within 10 days after HCT because of difficulty taking the medicine were 33.9%, 32.8%, and 60.0% (P = 0.063), respectively. With regard to chronic GVHD (cGVHD), taking DPP-4i between days 21 and 60 was associated with a trend toward lower incidence of cGVHD (1-year CI: 25.4% vs. 35.6%, P = 0.094). In a multivariate analysis, the administration of DPP-4i between days 21 and 60 was significantly associated with lower incidence of cGVHD (hazard ratio 0.53, 95% confidence interval 0.30–0.96, P = 0.035). It was difficult to interpret the impact of standard-dose DPP-4i on the development of aGVHD since an inability to continue oral medication was significantly associated with higher incidence of aGVHD. On the other hand, taking DPP-4i over days 21–60 may suppress the development of cGVHD.

Publisher

Research Square Platform LLC

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