Dasatinib-based 2-step induction for adults with Philadelphia chromosome–positive acute lymphoblastic leukemia

Author:

Sugiura Isamu1ORCID,Doki Noriko2,Hata Tomoko3,Cho Ryuko4,Ito Toshiro5,Suehiro Youko6,Tanaka Masatsugu7,Kako Shinichi8ORCID,Matsuda Mitsuhiro9ORCID,Yokoyama Hisayuki10ORCID,Ishikawa Yuichi11ORCID,Taniguchi Yasuhiro12,Hagihara Maki13,Ozawa Yukiyasu14,Ueda Yasunori15,Hirano Daiki16,Sakura Toru17,Tsuji Masaaki18,Kamae Tsuyoshi19,Fujita Hiroyuki20ORCID,Hiramoto Nobuhiro21,Onoda Masahiro22,Fujisawa Shin23,Hatta Yoshihiro24,Dobashi Nobuaki25,Nishiwaki Satoshi26,Atsuta Yoshiko2728,Kobayashi Yukio29,Hayakawa Fumihiko30,Ohtake Shigeki31ORCID,Naoe Tomoki16,Miyazaki Yasushi3

Affiliation:

1. Division of Hematology and Oncology, Toyohashi Municipal Hospital, Toyohashi, Japan;

2. Division of Hematology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Tokyo, Japan;

3. Department of Hematology, Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan;

4. Department of Hematology, Saiseikai Narashino Hospital, Chiba, Japan;

5. Department of Hematology, National Hospital Organization Matsumoto Medical Center, Matsumoto, Japan;

6. Department of Hematology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan;

7. Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan;

8. Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan;

9. Department of Hematology, PL General Hospital, Tondabayashi, Japan;

10. Department of Hematology, Sendai Medical Center, Sendai, Japan;

11. Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan;

12. Department of Hematology and Rheumatology, Kindai University Hospital, Osakasayama, Japan;

13. Department of Hematology and Clinical Immunology, Yokohama City University Hospital, Yokohama, Japan;

14. Department of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan;

15. Department of Hematology/Oncology, Kurashiki Central Hospital, Kurashiki, Japan;

16. Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan;

17. Leukemia Research Center, Saiseikai Maebashi Hospital, Maebashi, Japan;

18. Department of Hematology and Immunology, Otsu Red Cross Hospital, Otsu, Japan;

19. Department of Hematology, Otemae Hospital, Osaka, Japan;

20. Department of Hematology, Saiseikai Yokohama Nanbu Hospital, Yokohama, Japan;

21. Department of Hematology, Kobe City Medical Center General Hospital, Kobe, Japan;

22. Department of Hematology, Chiba Aoba Municipal Hospital, Chiba, Japan;

23. Department of Hematology, Yokohama City University Medical Center, Yokohama, Japan;

24. Department of Hematology and Rheumatology, Nihon University School of Medicine, Tokyo, Japan;

25. Division of Clinical Oncology/Hematology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan;

26. Department of Hematology, Nagoya University Hospital, Nagoya, Japan;

27. Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan;

28. Department of Registry Science for Transplant and Cellular Therapy, Aichi Medical University School of Medicine, Nagakute, Japan;

29. Department of Hematology, National Cancer Center Hospital, Tokyo, Japan;

30. Division of Cellular and Genetic Sciences, Department of Integrated Health Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan; and

31. Department of Hematology, Kanazawa University, Kanazawa, Japan

Abstract

Abstract The standard treatment for adults with Philadelphia chromosome–positive (Ph+) acute lymphoblastic leukemia (ALL) in Japan is imatinib-based chemotherapy followed by allogeneic hematopoietic stem cell transplantation (HSCT). However, ∼40% of patients cannot undergo HSCT in their first complete remission (CR1) because of chemotherapy-related toxicities or relapse before HSCT or older age. In this study, we evaluated dasatinib-based 2-step induction with the primary end point of 3-year event-free survival (EFS). The first induction (IND1) was dasatinib plus prednisolone to achieve CR, and IND2 was dasatinib plus intensive chemotherapy to achieve minimal residual disease (MRD) negativity. For patients who achieved CR and had an appropriate donor, HSCT during a consolidation phase later than the first consolidation, which included high-dose methotrexate, was recommended. Patients with pretransplantation MRD positivity were assigned to receive prophylactic dasatinib after HSCT. All 78 eligible patients achieved CR or incomplete CR after IND1, and 52.6% achieved MRD negativity after IND2. Nonrelapse mortality (NRM) was not reported. T315I mutation was detected in all 4 hematological relapses before HSCT. Fifty-eight patients (74.4%) underwent HSCT in CR1, and 44 (75.9%) had negative pretransplantation MRD. At a median follow-up of 4.0 years, 3-year EFS and overall survival were 66.2% (95% confidence interval [CI], 54.4-75.5) and 80.5% (95% CI, 69.7-87.7), respectively. The cumulative incidence of relapse and NRM at 3 years from enrollment were 26.1% and 7.8%, respectively. Dasatinib-based 2-step induction was demonstrated to improve 3-year EFS in Ph+ ALL. This study was registered in the UMIN Clinical Trial Registry as #UMIN000012173.

Publisher

American Society of Hematology

Subject

Hematology

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