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本文引用的文献

1
Anxiety and health-related quality of life among patients with low-tumor burden non-Hodgkin lymphoma randomly assigned to two different rituximab dosing regimens: results from ECOG trial E4402 (RESORT).随机分配至两种不同利妥昔单抗给药方案的低肿瘤负荷非霍奇金淋巴瘤患者的焦虑与健康相关生活质量:东部肿瘤协作组(ECOG)E4402试验(RESORT)结果
J Clin Oncol. 2015 Mar 1;33(7):740-8. doi: 10.1200/JCO.2014.57.6801. Epub 2015 Jan 20.
2
Safety and activity of lenalidomide and rituximab in untreated indolent lymphoma: an open-label, phase 2 trial.来那度胺和利妥昔单抗用于未经治疗的惰性淋巴瘤的安全性及活性:一项开放标签的2期试验
Lancet Oncol. 2014 Nov;15(12):1311-8. doi: 10.1016/S1470-2045(14)70455-3. Epub 2014 Oct 15.
3
Rituximab extended schedule or re-treatment trial for low-tumor burden follicular lymphoma: eastern cooperative oncology group protocol e4402.利妥昔单抗延长给药方案或再治疗用于低肿瘤负荷滤泡性淋巴瘤的试验:东部肿瘤协作组方案E4402
J Clin Oncol. 2014 Oct 1;32(28):3096-102. doi: 10.1200/JCO.2014.56.5853. Epub 2014 Aug 25.
4
Obinutuzumab plus chlorambucil in patients with CLL and coexisting conditions.奥滨尤妥珠单抗联合苯丁酸氮芥治疗伴有合并症的 CLL 患者。
N Engl J Med. 2014 Mar 20;370(12):1101-10. doi: 10.1056/NEJMoa1313984. Epub 2014 Jan 8.
5
Suboptimal dosing of rituximab in male and female patients with DLBCL.男性和女性弥漫性大 B 细胞淋巴瘤患者利妥昔单抗的剂量不足。
Blood. 2014 Jan 30;123(5):640-6. doi: 10.1182/blood-2013-07-517037. Epub 2013 Dec 2.
6
Persistence of minimal residual disease in bone marrow predicts outcome in follicular lymphomas treated with a rituximab-intensive program.骨髓中微小残留病的持续存在可预测采用利妥昔单抗强化方案治疗的滤泡性淋巴瘤的结局。
Blood. 2013 Nov 28;122(23):3759-66. doi: 10.1182/blood-2013-06-507319. Epub 2013 Oct 1.
7
Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia.伊布替尼治疗复发慢性淋巴细胞白血病的 BTK 靶点。
N Engl J Med. 2013 Jul 4;369(1):32-42. doi: 10.1056/NEJMoa1215637. Epub 2013 Jun 19.
8
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9
Phase II trial of individualized rituximab dosing for patients with CD20-positive lymphoproliferative disorders.CD20 阳性淋巴增殖性疾病患者利妥昔单抗个体化给药的 II 期试验。
J Clin Oncol. 2005 Feb 20;23(6):1096-102. doi: 10.1200/JCO.2005.12.171. Epub 2005 Jan 18.
10
Maximizing therapeutic benefit of rituximab: maintenance therapy versus re-treatment at progression in patients with indolent non-Hodgkin's lymphoma--a randomized phase II trial of the Minnie Pearl Cancer Research Network.最大化利妥昔单抗的治疗益处:惰性非霍奇金淋巴瘤患者的维持治疗与病情进展时再治疗——米妮·珀尔癌症研究网络的一项随机II期试验
J Clin Oncol. 2005 Feb 20;23(6):1088-95. doi: 10.1200/JCO.2005.12.191. Epub 2005 Jan 18.

利妥昔单抗延长给药方案或再治疗方案用于低肿瘤负荷非滤泡性惰性B细胞非霍奇金淋巴瘤:东部肿瘤协作组E4402方案

Rituximab extended schedule or retreatment trial for low tumour burden non-follicular indolent B-cell non-Hodgkin lymphomas: Eastern Cooperative Oncology Group Protocol E4402.

作者信息

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

机构信息

University of Virginia Cancer Center, Charlottesville, VA, USA.

Dana Farber Cancer Institute, Boston, MA, USA.

出版信息

Br J Haematol. 2016 Jun;173(6):867-75. doi: 10.1111/bjh.14007. Epub 2016 Mar 11.

DOI:10.1111/bjh.14007
PMID:26970533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4900920/
Abstract

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.

摘要

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。

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