TY - JOUR
T1 - Effect of allogeneic hematopoietic cell transplantation for patients with T-prolymphocytic leukemia
T2 - a retrospective study from the Adult Lymphoma Working Group of the Japan Society for hematopoietic cell transplantation
AU - Yamasaki, Satoshi
AU - Nitta, Hideaki
AU - Kondo, Eisei
AU - Uchida, Naoyuki
AU - Miyazaki, Takuya
AU - Ishiyama, Ken
AU - Kiyota, Miki
AU - Matsuoka, Hiroshi
AU - Ichinohe, Tatsuo
AU - Fukuda, Takahiro
AU - Atsuta, Yoshiko
AU - Suzumiya, Junji
AU - Suzuki, Ritsuro
N1 - Funding Information:
We appreciate the patients and clinical staff for their participation in the study. We are grateful to the Japanese Data Center for Hematopoietic Cell Transplantation for data management and the Clinical Research Institute of Kyushu Medical Hospital for their editorial support. We thank Ellen Knapp, PhD, from the Edanz Group (www.edanzediting.com) for editing a draft of this manuscript.
Funding Information:
This study was supported by The Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) of the Japan Agency for Medical Research and Development (AMED). Acknowledgments
Publisher Copyright:
© 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - 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.
AB - 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.
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U2 - 10.1007/s00277-019-03759-y
DO - 10.1007/s00277-019-03759-y
M3 - Article
C2 - 31327025
AN - SCOPUS:85069514027
SN - 0939-5555
VL - 98
SP - 2213
EP - 2220
JO - Annals of Hematology
JF - Annals of Hematology
IS - 9
ER -