TY - JOUR
T1 - The new generation tyrosine kinase inhibitor improves the survival of chronic myeloid leukemia patients after allogeneic stem cell transplantation
AU - the working group of the Japan Society for Transplantation and Cellular Therapy
AU - Shimazu, Yutaka
AU - Murata, Makoto
AU - Kondo, Takeshi
AU - Minami, Yosuke
AU - Tachibana, Takayoshi
AU - Doki, Noriko
AU - Uchida, Naoyuki
AU - Ozawa, Yukiyasu
AU - Yano, Shingo
AU - Fukuda, Takahiro
AU - Kato, Jun
AU - Ara, Takahide
AU - Eto, Testuya
AU - Ishikawa, Jun
AU - Nakamae, Hirohisa
AU - Tanaka, Junji
AU - Ichinohe, Tatsuo
AU - Atsuta, Yoshiko
AU - Nagamura-Inoue, Tokiko
N1 - Funding Information:
This study was conducted by the support of the chronic myeloid leukemia and myeloproliferative neoplasm working group in JSTCT. This study was supported in part by the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from the Japan Agency for Medical Research and Development (Grant 18ek0510023h0002).
Funding Information:
Makoto Murata has received honoraria from Kyowa Kirin, Sumitomo Dainippon Pharma, FUJIFILM, Toyama Chemical, Novartis Pharma, MSD, JCR Pharmaceuticals, Astellas Pharma, Miyarisan Pharmaceutical, Asahi Kasei Pharma, GlaxoSmithKline, Celgene, and Otsuka Pharmaceutical. Takayoshi Tachibana reports personal fees from Otsuka, personal fees from Novartis, personal fees from Pfizer, personal fees from BMS, personal fees from Daiichi Sankyo, personal fees from Astellas, outside the submitted work. Jun Kato has received honoraria from Kyowa Kirin, Novartis Pharma, JCR Pharmaceuticals, Astellas Pharma and Janssen Pharmaceutical K.K. outside the summited work. Hirohisa Nakamae has received honoraria and research funding from Bristol‐Myers Squibb, Novartis Pharma K.K., Otsuka Pharmaceutical Co., Ltd., and honoraria from Pfizer Inc. outside the submitted work. All the other authors declare no conflicts of interest.
Publisher Copyright:
© 2022 John Wiley & Sons Ltd.
PY - 2022/8
Y1 - 2022/8
N2 - The introduction of tyrosine kinase inhibitors (TKIs) in chronic myeloid leukemia (CML) treatment has dramatically improved the prognosis of CML patients and reduced the number of patients receiving allogeneic stem cell transplantation (allo-SCT). However, the impact of the newest-generation TKIs on the overall survival (OS) after allo-SCT has not been well described. To investigate the beneficial effects of TKIs on the prognosis after allo-SCT, we conducted a retrospective observational study using the Transplant Registry Unified Management Program database in Japan. We analyzed 1188 patients (male/female: 738/450; median age: 44 years; range: 16–75) who underwent their first allo-SCT between January 2001 and December 2018. We divided the patients into two groups according to the TKI treatment used before allo-SCT: group 1 was treated with the first generation TKI imatinib; group 2 was treated with the second generation TKIs nilotinib, dasatinib, or bosutinib and/or the third generation TKI ponatinib. We compared the post allo-SCT OS between the two groups. The 3-year OS rates (95%CI) of groups 1 and 2 were 59.3% (54.8%–63.5%) and 65.8% (61.6%–69.6%), respectively (p = 0.017). Multivariate analysis confirmed that group 2 had superior OS after allo-SCT compared to group 1 (p = 0.002). Other factors associated with superior prognosis were age ≤65, performance status (PS) 0/1, a 6/6 HLA-matched donor and chronic-phase (CP) disease status at allo-SCT. A subgroup analysis showed poor prognoses for patients who could not obtain a molecular response before allo-SCT and patients with positive T315I mutation in the BCR/ABL gene. In group 2, early allo-SCT was correlated with superior OS in patients with a blast-crisis disease status at allo-SCT (p = 0.001). The cumulative incidence of non-relapse mortality rate significantly decreased in group 2 (p = 0.0005). The post allo-SCT OS was improved both by pre- and post-management of allo-SCT and by the introduction of newer TKIs.
AB - The introduction of tyrosine kinase inhibitors (TKIs) in chronic myeloid leukemia (CML) treatment has dramatically improved the prognosis of CML patients and reduced the number of patients receiving allogeneic stem cell transplantation (allo-SCT). However, the impact of the newest-generation TKIs on the overall survival (OS) after allo-SCT has not been well described. To investigate the beneficial effects of TKIs on the prognosis after allo-SCT, we conducted a retrospective observational study using the Transplant Registry Unified Management Program database in Japan. We analyzed 1188 patients (male/female: 738/450; median age: 44 years; range: 16–75) who underwent their first allo-SCT between January 2001 and December 2018. We divided the patients into two groups according to the TKI treatment used before allo-SCT: group 1 was treated with the first generation TKI imatinib; group 2 was treated with the second generation TKIs nilotinib, dasatinib, or bosutinib and/or the third generation TKI ponatinib. We compared the post allo-SCT OS between the two groups. The 3-year OS rates (95%CI) of groups 1 and 2 were 59.3% (54.8%–63.5%) and 65.8% (61.6%–69.6%), respectively (p = 0.017). Multivariate analysis confirmed that group 2 had superior OS after allo-SCT compared to group 1 (p = 0.002). Other factors associated with superior prognosis were age ≤65, performance status (PS) 0/1, a 6/6 HLA-matched donor and chronic-phase (CP) disease status at allo-SCT. A subgroup analysis showed poor prognoses for patients who could not obtain a molecular response before allo-SCT and patients with positive T315I mutation in the BCR/ABL gene. In group 2, early allo-SCT was correlated with superior OS in patients with a blast-crisis disease status at allo-SCT (p = 0.001). The cumulative incidence of non-relapse mortality rate significantly decreased in group 2 (p = 0.0005). The post allo-SCT OS was improved both by pre- and post-management of allo-SCT and by the introduction of newer TKIs.
KW - allogeneic stem cell transplantation
KW - chronic myeloid leukemia
KW - tyrosine kinase inhibitor
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U2 - 10.1002/hon.3000
DO - 10.1002/hon.3000
M3 - Article
C2 - 35394658
AN - SCOPUS:85133535209
SN - 0278-0232
VL - 40
SP - 442
EP - 456
JO - Hematological Oncology
JF - Hematological Oncology
IS - 3
ER -