| Literature DB >> 35429328 |
Jin Hayakawa1, Hideki Nakasone1, Daisuke Minakata2, Shin-Ichiro Fujiwara2, Ayumi Gomyo1, Yu Akahoshi1, Yusuke Komiya1, Naonori Harada1, Tomotaka Ugai1, Kazuaki Kameda1, Hidenori Wada1, Yuko Ishihara1, Koji Kawamura1, Kana Sakamoto1, Miki Sato1, Kiriko Terasako-Saito1, Misato Kikuchi1, Shun-Ichi Kimura1, Junya Kanda1, Shinichi Kako1, Yoshinobu Kanda3,4.
Abstract
High-dose cytarabine (HD-AraC) or anthracycline-containing chemotherapies are used as post-remission therapy for acute myeloid leukemia (AML) patients. However, it remains unclear which regimen would be better as post-remission therapy before allogeneic hematopoietic stem cell transplantation (allo-HSCT). Thus, we compared the incidence of cardiac events and event-free survival (EFS) after allo-HSCT at two Japanese hospitals between HD-AraC and anthracycline-containing post-remission therapy to clarify the safety of post-remission therapy. Of a total of 132 patients, 68 received HD-AraC (HD-AraC group) and 64 received anthracycline-containing chemotherapy (ANT group). HD-AraC was preferentially selected for core-binding factor AML patients (p = 0.008). The median cumulative anthracycline dose was 115.2 mg/m2 in the HD-AraC group and 318.7 mg/m2 in the ANT group (p < 0.0001). Cardiac events were observed in 18 (13.6%) patients during the follow-up period. The 3-year cumulative incidence of cardiac events was 9.1% in the HD-AraC group and 11.0% in the ANT group (p = 0.70). EFS at 3 years after allo-HSCT was 40.9% in the HD-AraC group and 39.6% in the ANT group (p = 0.51). In conclusion, incidence of cardiac events did not differ significantly between post-remission therapy regimens in AML patients who underwent allo-HSCT.Entities:
Keywords: Acute myeloid leukemia; Anthracyclines; Bone marrow transplantation; Cardiotoxicity; Chemotherapy
Mesh:
Substances:
Year: 2022 PMID: 35429328 DOI: 10.1007/s12185-022-03343-7
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.319