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奥妥珠单抗联合来那度胺治疗晚期、既往未治疗且需要全身治疗的滤泡性淋巴瘤:一项LYSA研究。

Obinutuzumab plus lenalidomide in advanced, previously untreated follicular lymphoma in need of systemic therapy: a LYSA study.

作者信息

Bachy Emmanuel, Houot Roch, Feugier Pierre, Bouabdallah Krimo, Bouabdallah Reda, Virelizier Emmanuelle Nicolas, Maerevoet Marie, Fruchart Christophe, Snauwaert Sylvia, Le Gouill Steven, Marolleau Jean-Pierre, Molina Lysiane, Moluçon-Chabrot Cécile, Thieblemont Catherine, Tilly Hervé, Bijou Fontanet, Haioun Corinne, Van den Neste Eric, Fabiani Bettina, Meignan Michel, Cartron Guillaume, Salles Gilles, Casasnovas Olivier, Morschhauser Franck

机构信息

Hematology Department, Hospices Civils de Lyon, Lyon 1 Claude Bernard University, Lyon, France.

Hematology Department, CHU Rennes, Rennes, France.

出版信息

Blood. 2022 Apr 14;139(15):2338-2346. doi: 10.1182/blood.2021013526.

Abstract

Obinutuzumab and lenalidomide (referred to as the GALEN combination) is an active immunomodulatory combination with a manageable safety profile in multiple types of lymphoma. We report efficacy and safety results for the phase 2 GALEN study in previously untreated patients with advanced follicular lymphoma (FL). Eligible patients aged ≥18 years had an Eastern Cooperative Oncology Group performance status ≤2 and high-tumor burden, grade 1 to 3a FL. Induction treatment was obinutuzumab (1000 mg IV, days 8, 15, and 22, cycle 1; day 1, cycles 2-6) plus lenalidomide (20 mg/d, days 1-21, cycle 1; days 2-22, cycles 2-6) for six 28-day cycles. Maintenance included obinutuzumab (1000 mg every 2 cycles) plus lenalidomide (10 mg, days 2-22) for ≤12 cycles (year 1) followed by obinutuzumab (1000 mg every 56 days) for 6 cycles (year 2). The primary end point was complete response rate (CRR) after induction per the 1999 International Working Group criteria. From October 2015 to February 2017, a total of 100 patients were enrolled. CRR after induction was 47%, and the overall response rate (ORR) was 92%. Post hoc analyses per the 2014 Lugano classification, including patients with missing bone marrow assessments, identified an additional 13 patients fulfilling CRR criteria, resulting in a complete metabolic response of 80% and an ORR of 94%. At a median follow-up of 3.7 years, 3-year progression-free survival and overall survival were 82% and 94%, respectively. The most common adverse event was neutropenia (48% any grade; 47% grade ≥3). Only 2% of patients presented with febrile neutropenia; others were mainly grade ≤2. No other specific grade ≥3 toxicity occurred at a frequency >3%. Overall, these results showed promising clinical efficacy for the chemotherapy-free GALEN backbone in previously untreated patients with high tumor burden FL. Except for neutropenia, the safety profile of the combination is remarkable. The study was registered at clinicaltrials.gov as #NCT01582776.

摘要

奥妥珠单抗和来那度胺(称为GALEN组合)是一种具有活性的免疫调节组合,在多种类型淋巴瘤中具有可控的安全性。我们报告了GALEN 2期研究在先前未治疗的晚期滤泡性淋巴瘤(FL)患者中的疗效和安全性结果。符合条件的患者年龄≥18岁,东部肿瘤协作组体能状态≤2且肿瘤负荷高,为1至3a级FL。诱导治疗为奥妥珠单抗(静脉注射1000 mg,第1周期第8、15和22天;第2至6周期第1天)加来那度胺(20 mg/d,第1周期第1至21天;第2至6周期第2至22天),共六个28天周期。维持治疗包括奥妥珠单抗(每2个周期1000 mg)加来那度胺(10 mg,第2至22天),共≤12个周期(第1年),随后奥妥珠单抗(每56天1000 mg),共6个周期(第2年)。主要终点是根据1999年国际工作组标准诱导后的完全缓解率(CRR)。2015年10月至2017年2月,共入组100例患者。诱导后的CRR为47%,总缓解率(ORR)为92%。根据2014年卢加诺分类进行的事后分析,包括骨髓评估缺失的患者,又有13例患者符合CRR标准,导致完全代谢缓解率为80%,ORR为94%。中位随访3.7年时,3年无进展生存率和总生存率分别为82%和94%。最常见的不良事件是中性粒细胞减少(任何级别48%;≥3级47%)。仅2%的患者出现发热性中性粒细胞减少;其他主要为≤2级。无其他特定的≥3级毒性发生率>3%。总体而言,这些结果显示,对于先前未治疗、肿瘤负荷高的FL患者,无化疗的GALEN方案具有良好的临床疗效。除中性粒细胞减少外,该组合的安全性显著。该研究在clinicaltrials.gov上注册为#NCT01582776。

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