当前位置: X-MOL 学术Int. J. Hematol. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Successful outcome with reduced-intensity condition regimen followed by allogeneic hematopoietic stem cell transplantation for relapsed or refractory anaplastic large-cell lymphoma.
International Journal of Hematology ( IF 2.1 ) Pub Date : 2019-10-18 , DOI: 10.1007/s12185-019-02748-1
Reiji Fukano 1, 2 , Tetsuya Mori 3 , Naoto Fujita 4 , Ryoji Kobayashi 5 , Tetsuo Mitsui 6 , Koji Kato 7 , Ritsuro Suzuki 8 , Junji Suzumiya 8 , Takahiro Fukuda 9 , Motohiro Shindo 10 , Nobuo Maseki 11 , Tatsu Shimoyama 12 , Keiko Okada 13 , Masami Inoue 14 , Jiro Inagaki 1 , Yoshiko Hashii 15 , Atsushi Sato 16 , Ken Tabuchi 17
Affiliation  

We report a retrospective analysis of 38 patients (age ≤ 30 years) who underwent allogeneic hematopoietic stem cell transplantation (allo-SCT) for relapsed or refractory anaplastic large-cell lymphoma (ALCL). Median follow-up for survivors after undergoing allo-SCT was 72 months (range, 35-96 months). Eight patients received reduced-intensity conditioning (RIC) regimens, including three patients with fludarabine plus melphalan-based regimens and five patients with fludarabine plus busulfan-based regimens. The remaining 30 patients received myeloablative conditioning (MAC) regimens. Median ages in the RIC and MAC groups were 24 and 15 years, respectively. The 5-year overall survival rates in the RIC and MAC groups were 100% and 49%, respectively (P = 0.018). The 5-year event-free survival rates in the RIC and MAC groups were 88% and 43%, respectively (P = 0.039). In the RIC group, four of the eight patients showed residual disease at allo-SCT, but all eight patients survived with complete remission (CR), including one patient with relapse. This result suggests that allo-SCT using the RIC regimen may be effective for relapsed or refractory ALCL in children, adolescents, and young adults, even in non-CR cases.

中文翻译:

强度降低的治疗方案的成功结果,然后是异基因造血干细胞移植,用于复发性或难治性间变性大细胞淋巴瘤。

我们报告回顾性分析38例(年龄≤30岁)接受异基因造血干细胞移植(allo-SCT)治疗的复发性或难治性间变性大细胞淋巴瘤(ALCL)。接受异基因SCT后幸存者的中位随访时间为72个月(范围为35-96个月)。8例患者接受了降低强度调理(RIC)方案,包括3例氟达拉滨加美法仑治疗方案的患者和5例氟达拉滨加白消安方案的患者。其余30例患者接受了清髓治疗(MAC)方案。RIC和MAC组的中位年龄分别为24岁和15岁。RIC和MAC组的5年总生存率分别为100%和49%(P = 0.018)。RIC和MAC组的5年无事件生存率分别为88%和43%,分别为(P = 0.039)。在RIC组中,八名患者中有四名在allo-SCT上表现出残留病灶,但八名患者全部存活下来,完全缓解(CR),包括一名复发患者。该结果表明,使用RIC方案的allo-SCT可能对儿童,青少年和年轻人的复发或难治性ALCL有效,即使在非CR病例中也是如此。
更新日期:2019-10-16
down
wechat
bug