TY - JOUR
T1 - Haematopoietic stem cell transplantation for relapsed or refractory anaplastic large cell lymphoma
T2 - A study of children and adolescents in Japan
AU - Fukano, Reiji
AU - Mori, Tetsuya
AU - Kobayashi, Ryoji
AU - Mitsui, Tetsuo
AU - Fujita, Naoto
AU - Iwasaki, Fuminori
AU - Suzumiya, Junji
AU - Chin, Motoaki
AU - Goto, Hiroaki
AU - Takahashi, Yoshiyuki
AU - Hara, Junichi
AU - Park, Yong Dong
AU - Inoue, Masami
AU - Koga, Yuhki
AU - Inagaki, Jiro
AU - Sakamaki, Hisashi
AU - Adachi, Souichi
AU - Kawa, Keisei
AU - Kato, Koji
AU - Suzuki, Ritsuro
N1 - Publisher Copyright:
© 2014 John Wiley & Sons Ltd.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Summary: To evaluate haematopoietic stem cell transplantation (HSCT) in children and adolescents, we reviewed the records of 47 patients who were ≤18 years, had relapsed or refractory anaplastic large cell lymphoma, and received HSCT between 1990 and 2010. At HSCT, complete remission (CR) was less common in allogeneic HSCT recipients (n = 24) than in autologous HSCT recipients (n = 23) (P = 0·01). The autologous and allogeneic HSCT groups differed in terms of 5-year event-free survival (EFS) (38% vs. 50%, P = 0·63), cumulative incidence of progress or relapse (49% vs. 28%, P = 0·25), and treatment-related mortality (12% vs. 25%, P = 0·40). However, these differences were not significant. Patients with non-CR at autologous HSCT had a significantly lower EFS rate (14% vs. 48%, P = 0·03). Conversely, although those with non-CR at allogeneic HSCT had a lower EFS rate, this was not significant (44% vs. 63%, P = 0·26). Reduced-intensity conditioning regimens were used for three of the 16 allogeneic HSCTs received by patients with non-CR. These three patients achieved CR, surviving 32-65 months after HSCT. These results demonstrated that allogeneic HSCT might be a treatment option for patients who do not achieve CR through conventional chemotherapy.
AB - Summary: To evaluate haematopoietic stem cell transplantation (HSCT) in children and adolescents, we reviewed the records of 47 patients who were ≤18 years, had relapsed or refractory anaplastic large cell lymphoma, and received HSCT between 1990 and 2010. At HSCT, complete remission (CR) was less common in allogeneic HSCT recipients (n = 24) than in autologous HSCT recipients (n = 23) (P = 0·01). The autologous and allogeneic HSCT groups differed in terms of 5-year event-free survival (EFS) (38% vs. 50%, P = 0·63), cumulative incidence of progress or relapse (49% vs. 28%, P = 0·25), and treatment-related mortality (12% vs. 25%, P = 0·40). However, these differences were not significant. Patients with non-CR at autologous HSCT had a significantly lower EFS rate (14% vs. 48%, P = 0·03). Conversely, although those with non-CR at allogeneic HSCT had a lower EFS rate, this was not significant (44% vs. 63%, P = 0·26). Reduced-intensity conditioning regimens were used for three of the 16 allogeneic HSCTs received by patients with non-CR. These three patients achieved CR, surviving 32-65 months after HSCT. These results demonstrated that allogeneic HSCT might be a treatment option for patients who do not achieve CR through conventional chemotherapy.
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U2 - 10.1111/bjh.13167
DO - 10.1111/bjh.13167
M3 - Article
C2 - 25312752
AN - SCOPUS:84923091418
SN - 0007-1048
VL - 168
SP - 557
EP - 563
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 4
ER -