| Literature DB >> 31327025 |
Satoshi Yamasaki1, Hideaki Nitta2, Eisei Kondo3, Naoyuki Uchida4, Takuya Miyazaki5, Ken Ishiyama6, Miki Kiyota7, Hiroshi Matsuoka8, Tatsuo Ichinohe9, Takahiro Fukuda10, Yoshiko Atsuta11, Junji Suzumiya12, Ritsuro Suzuki12.
Abstract
Alemtuzumab is the treatment choice for patients with T-prolymphocytic leukemia (T-PLL). However, patients with T-PLL have a poor prognosis, and the option of allogeneic hematopoietic cell transplantation (HCT) remains controversial in these patients. This study aimed to analyze the outcomes of allogeneic HCT among patients with T-PLL to identify the potential clinical efficacy of allogeneic HCT. We retrospectively analyzed data from 20 patients with T-PLL, including five patients with complex chromosomal abnormalities at diagnosis who received an allogeneic HCT between 2000 and 2016. The median follow-up of survivors was 51 months in allogeneic HCT from human leukemia antigen (HLA)-matched donors. All five patients with complex chromosomal abnormalities died after allogeneic HCT. Our data suggest that allogeneic HCT from an HLA-matched donor can be considered for patients with T-PLL without complex chromosomal abnormalities. New treatment strategies of allogeneic HCT are required to improve the safety and efficacy of allografting in patients with T-PLL and complex chromosomal abnormalities. Potential approaches that identify patients with T-PLL and complex chromosomal abnormalities for allogeneic HCT with better disease control may allow identification of individuals who are suitable for allogeneic HCT.Entities:
Keywords: Allogeneic hematopoietic cell transplantation; Complex chromosomal abnormalities; HLA-matched donor; T-prolymphocytic leukemia
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Year: 2019 PMID: 31327025 DOI: 10.1007/s00277-019-03759-y
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673