TY - JOUR
T1 - The outcome and characteristics of patients with relapsed adult T cell leukemia/lymphoma after allogeneic hematopoietic stem cell transplantation
AU - ATL Working Group of the Japan Society for Hematopoietic Cell Transplantation
AU - Kato, Koji
AU - Uike, Naokuni
AU - Wake, Atsushi
AU - Yoshimitsu, Makoto
AU - Tobai, Tomomi
AU - Sawayama, Yasushi
AU - Takatsuka, Yoshifusa
AU - Fukuda, Takahiro
AU - Uchida, Naoyuki
AU - Eto, Tetsuya
AU - Nakashima, Yasuhiro
AU - Kondo, Tadakazu
AU - Taguchi, Jun
AU - Miyamoto, Toshihiro
AU - Nakamae, Hirohisa
AU - Ichinohe, Tatsuo
AU - Kato, Koji
AU - Suzuki, Ritsuro
AU - Utsunomiya, Atae
N1 - Funding Information:
We thank the physicians and data managers at the institutions who contributed valuable data regarding ATLL‐related transplantation to JSHCT. We thank all members of the data management committees of JSHCT. This work was supported in part by the Japan Agency for Medical Research and Development Grant Number 15Ack0106136h0002 (Koji Kato and Takahiro Fukuda).
Publisher Copyright:
© 2018 John Wiley & Sons, Ltd.
PY - 2019/2
Y1 - 2019/2
N2 - Treatment options for patients with adult T cell leukemia/lymphoma (ATLL) who have relapsed disease after allogeneic hematopoietic stem cell transplantation (allo-HSCT) are limited. To clarify which patients with ATLL are likely to benefit from these treatment options and to define patient populations for novel treatments, we performed a nationwide retrospective analysis of 252 Japanese patients who had relapsed ATLL after allo-HSCT. Some long-term survivors remained after tapering and withdrawal of immunosuppressive agents. Thirty-six patients who received donor lymphocyte infusion had a better overall survival (OS) in comparison to those who did not [hazard ratio (HR), 0.63; 95% confidence interval (CI), 0.43-0.93; P =.02], suggesting the efficacy of a graft-versus-ATLL (GvATLL) effect even after relapse. Multivariate analysis demonstrated that skin lesions at initial relapse of ATLL were independently associated with higher OS (HR, 0.41; 95% CI, 0.22-0.74; P =.003), indicating that the skin is a susceptible target organ of GvATLL. This study suggested that enhancement of a GvATLL effect is a potential therapeutic option for relapsed disease after allo-HSCT. Further investigations of incorporation of immune-based approaches with new molecular target drugs into the therapeutic options of patients with ATLL before and after transplantation are warranted.
AB - Treatment options for patients with adult T cell leukemia/lymphoma (ATLL) who have relapsed disease after allogeneic hematopoietic stem cell transplantation (allo-HSCT) are limited. To clarify which patients with ATLL are likely to benefit from these treatment options and to define patient populations for novel treatments, we performed a nationwide retrospective analysis of 252 Japanese patients who had relapsed ATLL after allo-HSCT. Some long-term survivors remained after tapering and withdrawal of immunosuppressive agents. Thirty-six patients who received donor lymphocyte infusion had a better overall survival (OS) in comparison to those who did not [hazard ratio (HR), 0.63; 95% confidence interval (CI), 0.43-0.93; P =.02], suggesting the efficacy of a graft-versus-ATLL (GvATLL) effect even after relapse. Multivariate analysis demonstrated that skin lesions at initial relapse of ATLL were independently associated with higher OS (HR, 0.41; 95% CI, 0.22-0.74; P =.003), indicating that the skin is a susceptible target organ of GvATLL. This study suggested that enhancement of a GvATLL effect is a potential therapeutic option for relapsed disease after allo-HSCT. Further investigations of incorporation of immune-based approaches with new molecular target drugs into the therapeutic options of patients with ATLL before and after transplantation are warranted.
UR - http://www.scopus.com/inward/record.url?scp=85054011475&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85054011475&partnerID=8YFLogxK
U2 - 10.1002/hon.2558
DO - 10.1002/hon.2558
M3 - Article
C2 - 30171618
AN - SCOPUS:85054011475
SN - 0278-0232
VL - 37
SP - 54
EP - 61
JO - Hematological Oncology
JF - Hematological Oncology
IS - 1
ER -