Outcome of allogeneic hematopoietic stem cell transplantation for mycosis fungoides and Sezary syndrome

被引:12
|
作者
Mori, Takehiko [1 ]
Shiratori, Souichi [2 ]
Suzumiya, Junji [3 ]
Kurokawa, Mineo [4 ]
Shindo, Motohiro [5 ]
Naoyuki, Uchida [6 ]
Katsuto, Takenaka [7 ]
Miyamoto, Toshihiro [8 ]
Morishige, Satoshi [9 ]
Hirokawa, Makoto [10 ]
Fukuda, Takahiro [11 ]
Atsuta, Yoshiko [12 ,13 ]
Suzuki, Ritsuro [3 ]
机构
[1] Keio Univ, Dept Med, Div Hematol, Sch Med, Tokyo, Japan
[2] Hokkaido Univ, Dept Hematol, Fac Med, Sapporo, Hokkaido, Japan
[3] Shimane Univ, Sch Med, Dept Oncol Hematol, Matsue, Shimane, Japan
[4] Univ Tokyo Hosp, Dept Cell Therapy & Transplantat Med, Tokyo, Japan
[5] Asahikawa Med Univ, Div Gastroenterol & Hematol Oncol, Dept Med, Asahikawa, Hokkaido, Japan
[6] Toranomon Gen Hosp, Dept Hematol, Federat Natl Publ Serv Personnel Mutual Aid Assoc, Tokyo, Japan
[7] Ehime Univ Hosp, Dept Internal Med 1, Toon, Ehime, Japan
[8] Kyushu Univ, Grad Sch Med Sci, Med & Biosyst Sci, Fukuoka, Japan
[9] Kurume Univ Hosp, Dept Med, Div Hematol & Oncol, Kurume, Fukuoka, Japan
[10] Akita Univ, Dept Gen Internal Med & Clin Lab Med, Grad Sch Med, Akita, Japan
[11] Natl Canc Ctr, Hematopoiet Stem Cell Transplantat Div, Tokyo, Japan
[12] Japanese Data Ctr Hematopoiet Cell Transplantat, Nagoya, Aichi, Japan
[13] Nagoya Univ, Dept Healthcare Adm, Grad Sch Med, Nagoya, Aichi, Japan
关键词
allogeneic hematopoietic stem cell transplantation; mycosis fungoides; Sezary syndrome; T-CELL; LYMPHOMA; MULTICENTER; BLOOD;
D O I
10.1002/hon.2719
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although allogeneic hematopoietic stem cell transplantation (HSCT) has been reported to provide prolonged remission of relapsed/refractory mycosis fungoides (MF) and Sezary syndrome (SS), its role has not been fully evaluated. Here, the outcomes of allogeneic HSCT for patients with MF/SS were retrospectively evaluated by using the registry database of the Japan Society for Hematopoietic Cell Transplantation. Forty-eight patients were evaluable and enrolled in the analysis. Median age was 45.5 years. Eighteen patients (38%) received myeloablative conditioning, and 33 (69%) received HSCT from an alternative donor. Disease status was complete or partial response in 25% of the patients and relapsed or refractory in the others. At the time of analysis, 18 patients were alive, with a median follow-up of 31.0 months (range, 3.8-31.1). Three-year overall survival (OS) and progression-free survival (PFS) were 30% (95%CI, 16-45%) and 19% (95%CI, 9-31%), respectively. Disease progression was not observed later than 17 months after transplantation. Both disease status and performance status at transplant significantly affected OS and PFS. Although our findings suggest that allogeneic HSCT provides long-term PFS in patients with MF/SS, the timing of transplantation should be decided carefully based on the disease status and the patient's condition in order to improve the outcome.
引用
收藏
页码:266 / 271
页数:6
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