a Cardinal Bernardin Cancer Center, Loyola University Medical Center , Maywood , IL , USA.
b SWOG Statistical Center , Seattle , WA , USA.
Leuk Lymphoma. 2019 Aug;60(8):1934-1941. doi: 10.1080/10428194.2018.1563691. Epub 2019 Jan 10.
Phase II data suggest a benefit to autotransplantation for aggressive T-cell non-Hodgkin lymphoma (T-NHL) in first remission; randomized trials have yet to validate this. We performed a retrospective analysis of aggressive T-NHL patients in the intergroup randomized consolidative autotransplant trial (SWOG 9704). Of the 370 enrolled, 40 had T-NHL: 12 were not randomized due to ineligibility ( = 1), choice ( = 2), or progression ( = 9), leaving 13 randomized to control and 15 to autologous stem cell transplantation (ASCT). Two ASCT patients refused transplant and one failed mobilization. The 5-year landmark PFS/OS estimates for ASCT vs. control groups were 40% vs. 38% ( = .56), and 40% vs. 45% ( = .98), respectively. No difference was seen based on IPI, or histologic subtype. Only 1/7 receiving BCNU-based therapy survived vs. 4/5 receiving TBI. Aggressive T-NHL autotransplanted in first remission did not appear to benefit from consolidative ASCT. This and the 30% who dropped out pre-randomization mostly to progression, suggests that improved induction regimens be developed.
二期数据表明,在首次缓解期对侵袭性 T 细胞非霍奇金淋巴瘤(T-NHL)进行自体移植有获益;但随机试验尚未证实这一点。我们对随机分组巩固性自体移植试验(SWOG 9704)中的侵袭性 T-NHL 患者进行了回顾性分析。在纳入的 370 例患者中,有 40 例为 T-NHL:12 例因不适合( = 1)、选择( = 2)或进展( = 9)而未随机分组,13 例随机分组至对照组,15 例随机分组至自体造血干细胞移植(ASCT)组。2 例 ASCT 患者拒绝移植,1 例动员失败。ASCT 组与对照组的 5 年 landmark PFS/OS 估计值分别为 40%与 38%( = .56),40%与 45%( = .98)。基于 IPI 或组织学亚型未观察到差异。仅 1/7 例接受 BCNU 为基础的治疗的患者存活,而接受 TBI 治疗的患者中 4/5 例存活。在首次缓解期接受自体移植的侵袭性 T-NHL 似乎并未从巩固性 ASCT 中获益。这与 30%在随机分组前因进展而退出的患者表明,需要开发更好的诱导方案。