| Literature DB >> 35394258 |
Chikashi Yoshida1, Takeshi Kondo2, Tomoki Ito3, Masahiro Kizaki4, Kazuhiko Yamamoto5, Toshihiro Miyamoto6, Yasuyoshi Morita7, Tetsuya Eto8, Yuna Katsuoka9, Naoki Takezako10, Nobuhiko Uoshima11, Kazunori Imada12, Jun Ando13, Takuya Komeno14, Akio Mori2, Yuichi Ishikawa15, Atsushi Satake3, Junichi Watanabe4, Yoshiko Kawakami16, Tetsuo Morita16, Ikue Taneike16, Masahiko Nakayama16, Yinghui Duan17, Belen Garbayo Guijarro18, Alexander Delgado19, Cynthia Llamas17, Hitoshi Kiyoi15.
Abstract
Acute myeloid leukemia (AML) predominantly affects elderly adults, and its prognosis worsens with age. Treatment options for patients in Japan ineligible for intensive chemotherapy include cytarabine/aclarubicin ± granulocyte colony-stimulating factor (CA ± G), azacitidine (AZA), low-dose cytarabine (LDAC), targeted therapy, and best supportive care (BSC). The country's aging population and the evolving treatment landscape are contributing to a need to understand treatment pathways and associated outcomes. This retrospective chart review evaluated outcomes in patients across Japan with primary/secondary AML who were ineligible for intensive chemotherapy and began first-line treatment or BSC between 01/01/2015 and 12/31/2018. The primary endpoint was overall survival (OS); secondary endpoints included progression-free survival (PFS) and healthcare resource utilization (HRU). Of 199 patients (58% > 75 years), 121 received systemic therapy (38 CA ± G, 37 AZA, 7 LDAC, 39 other) and 78 received BSC. Median OS was 5.4, 9.2, 2.2, 3.8, and 2.2 months for CA ± G, AZA, LDAC, other systemic therapy, and BSC, respectively; median PFS was 3.4, 7.7, 1.6, 2.3, and 2.1 months, respectively. HRU rates were uniformly high, with > 80% patients hospitalized in each cohort. The poor clinical outcomes and high HRU among Japanese AML patients who are ineligible for intensive chemotherapy highlight an unmet need for novel therapies.Entities:
Keywords: Aclarubicin ± granulocyte colony-stimulating factor; Acute myeloid leukemia; Azacitidine; Low-dose cytarabine
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Year: 2022 PMID: 35394258 DOI: 10.1007/s12185-022-03334-8
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490