Williams Michael E, Hong Fangxin, Gascoyne Randy D, Wagner Lynne I, Krauss John C, Habermann Thomas M, Swinnen Lode J, Schuster Stephen J, Peterson Christopher G, Sborov Mark D, Martin S Eric, Weiss Matthias, Ehmann W Christopher, Horning Sandra J, Kahl Brad S
University of Virginia Cancer Center, Charlottesville, VA, USA.
Dana Farber Cancer Institute, Boston, MA, USA.
Br J Haematol. 2016 Jun;173(6):867-75. doi: 10.1111/bjh.14007. Epub 2016 Mar 11.
The rituximab extended schedule or retreatment trial (RESORT; E4402) was a phase 3 randomized prospective trial comparing maintenance rituximab (MR) versus a retreatment (RR) dosing strategy in asymptomatic, low tumour burden indolent lymphoma. A planned exploratory sub-study compared the two strategies for small lymphocytic (SLL) and marginal zone lymphomas (MZL). Patients responding to rituximab weekly × 4 were randomized to MR (single dose rituximab every 3 months until treatment failure) or RR (rituximab weekly × 4) at the time of each progression until treatment failure. The primary endpoint was time to treatment failure (TTTF). Patients with SLL (n = 57), MZL (n = 71) and unclassifiable small B-cell lymphoma (n = 3) received induction rituximab. The overall response rate (ORR) was 40% [95% confidence interval (CI) 31-49%; SLL ORR 22·8%; MZL ORR 52·1%]; all 52 responders were randomized. At a median of 4·3 years from randomization, treatment failure occurred in 18/23 RR and 15/29 MR. The median TTTF was 1·4 years for RR and 4·8 years for MR (P = 0·012); median time to first cytotoxic therapy was 6·3 years for RR and not reached for MR (P = 0·0002). Survival did not differ (P = 0·72). In low tumour burden SLL and MZL patients responding to rituximab induction, MR significantly improved TTTF as compared with RR.
利妥昔单抗延长给药方案或再治疗试验(RESORT;E4402)是一项3期随机前瞻性试验,比较了在无症状、低肿瘤负荷的惰性淋巴瘤中维持使用利妥昔单抗(MR)与再治疗(RR)给药策略。一项计划中的探索性子研究比较了小淋巴细胞淋巴瘤(SLL)和边缘区淋巴瘤(MZL)的这两种策略。对每周一次×4次利妥昔单抗治疗有反应的患者,在每次病情进展时随机分为MR组(每3个月单剂量利妥昔单抗,直至治疗失败)或RR组(每周一次×4次利妥昔单抗),直至治疗失败。主要终点是至治疗失败时间(TTTF)。SLL患者(n = 57)、MZL患者(n = 71)和无法分类的小B细胞淋巴瘤患者(n = 3)接受了诱导性利妥昔单抗治疗。总缓解率(ORR)为40%[95%置信区间(CI)31 - 49%;SLL的ORR为22.8%;MZL的ORR为52.1%];所有52名缓解者均被随机分组。随机分组后中位4.3年时,RR组23例中有18例出现治疗失败,MR组29例中有15例出现治疗失败。RR组的中位TTTF为1.4年,MR组为4.8年(P = 0.012);RR组至首次细胞毒性治疗的中位时间为6.3年,MR组未达到(P = 0.0002)。生存率无差异(P = 0.72)。在对利妥昔单抗诱导治疗有反应的低肿瘤负荷SLL和MZL患者中,与RR相比,MR显著改善了TTTF。