Division of Hematology/Oncology, Tufts University School of Medicine, Boston, Massachusetts.
Cancer. 2013 Oct 15;119(20):3662-71. doi: 10.1002/cncr.28243. Epub 2013 Aug 6.
Stem cell transplant (SCT)-related outcomes and prognostication for relapsed/refractory follicular lymphoma (FL) are not well-defined in the post-rituximab era.
Through the National Comprehensive Cancer Network (NCCN) lymphoma outcomes study, 184 patients with relapsed/refractory FL who underwent autologous SCT (autoSCT) or allogenic SCT (alloSCT) following disease relapse after prior rituximab-based therapy were examined.
Patients who underwent autoSCT (N=136) were older compared with patients who underwent alloSCT (N=48) (54 versus 51 years, respectively, P=.01) and more frequently had grade 3 FL (35% versus 8%, respectively, P=.006). Patients who underwent alloSCT received more prior therapies (4 versus 3, respectively, P<.0001) and more often had resistant disease at SCT (19% versus 6%, respectively, P=.008). Cumulative 100-day nonrelapse mortality (NRM) for autoSCT and alloSCT were 1% and 6%, respectively (P<.0001), whereas 3-year NRM rates were 3% versus 24%, respectively (P<.0001). For autoSCT and alloSCT, cumulative rates of relapse, progression, and/or transformation were 32% versus 16%, respectively (P=.03), whereas 3-year overall survival rates were 87% versus 61% (P<.0001); there were no differences in failure-free survival. AlloSCT was associated with increased risk of death on multivariate analysis (hazard ratio=2.77, 95% confidence interval=1.46-5.26, P=.002). This finding persisted on propensity scoring/matching. Multivariate analysis for autoSCT patients identified age>60 years and>3 prior therapies as adverse factors. Furthermore, a survival model was created for the autoSCT cohort based on number of factors present (0, 1, 2); 3-year failure-free survival was 72%, 47%, and 20%, respectively (P=.0003), and 3-year overall survival was 96%, 82%, and 62%, respectively (P<.0001).
AutoSCT remains an effective therapy for patients with FL. For alloSCT, continued strategies to reduce NRM are needed.
在利妥昔单抗时代,干细胞移植(SCT)相关结局和复发性/难治性滤泡淋巴瘤(FL)的预后尚不清楚。
通过国家综合癌症网络(NCCN)淋巴瘤结局研究,对 184 例在先前基于利妥昔单抗的治疗后疾病复发后接受自体 SCT(autoSCT)或同种异体 SCT(alloSCT)的复发性/难治性 FL 患者进行了检查。
接受 autoSCT(N=136)的患者比接受 alloSCT(N=48)的患者年龄更大(分别为 54 岁和 51 岁,P=.01),并且更常患有 3 级 FL(分别为 35%和 8%,P=.006)。接受 alloSCT 的患者接受了更多的先前治疗(分别为 4 次和 3 次,P<.0001),并且在 SCT 时更常患有耐药疾病(分别为 19%和 6%,P=.008)。autoSCT 和 alloSCT 的 100 天累积非复发死亡率(NRM)分别为 1%和 6%(P<.0001),而 3 年 NRM 率分别为 3%和 24%(P<.0001)。对于 autoSCT 和 alloSCT,累积复发、进展和/或转化率分别为 32%和 16%(P=.03),而 3 年总生存率分别为 87%和 61%(P<.0001);无失败生存率无差异。多变量分析显示 alloSCT 与死亡风险增加相关(风险比=2.77,95%置信区间=1.46-5.26,P=.002)。在倾向评分/匹配后,这一发现仍然存在。多变量分析发现年龄>60 岁和>3 次先前治疗是不利因素。此外,根据存在的因素数量(0、1、2)为 autoSCT 队列创建了一个生存模型;3 年无失败生存率分别为 72%、47%和 20%(P=.0003),3 年总生存率分别为 96%、82%和 62%(P<.0001)。
AutoSCT 仍然是 FL 患者的有效治疗方法。对于 alloSCT,需要继续采取策略来降低 NRM。