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

Although allogeneic hematopoietic stem cell transplantation (HSCT) has been reported to provide prolonged remission of relapsed/refractory mycosis fungoides (MF) and Sézary syndrome (SS), its role has not been fully evaluated. Here, the outcomes of allogeneic HSCT for patients with MF/SS were retros...

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Veröffentlicht in:Hematological oncology 2020-08, Vol.38 (3), p.266-271
Hauptverfasser: Mori, Takehiko, Shiratori, Souichi, Suzumiya, Junji, Kurokawa, Mineo, Shindo, Motohiro, Naoyuki, Uchida, Katsuto, Takenaka, Miyamoto, Toshihiro, Morishige, Satoshi, Hirokawa, Makoto, Fukuda, Takahiro, Atsuta, Yoshiko, Suzuki, Ritsuro
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Sprache:eng
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Zusammenfassung:Although allogeneic hematopoietic stem cell transplantation (HSCT) has been reported to provide prolonged remission of relapsed/refractory mycosis fungoides (MF) and Sézary 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.
ISSN:0278-0232
1099-1069
DOI:10.1002/hon.2719