Service d'hématologie clinique du Centre Hospitalier Universitaire (CHU) de Nantes, INSERM Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA) Nantes-Angers, Nantes Excellence Trajectory (NeXT) Université de Nantes, Nantes, France.
CHU Lille, Université de Lille, Lille, France.
Blood. 2021 Feb 18;137(7):877-887. doi: 10.1182/blood.2020008727.
Ibrutinib, obinutuzumab, and venetoclax demonstrate synergy in preclinical models of mantle cell lymphoma (MCL). OAsIs (NCT02558816), a single-arm multicenter prospective phase 1/2 trial, aimed to determine the maximum tolerated dose of venetoclax in combination with fixed doses of ibrutinib and obinutuzumab, in relapsed MCL patients. At the venetoclax MTD, extension cohorts were opened for relapsed and untreated patients. Safety and efficacy were secondary objectives. Minimal residual disease (MRD) was assessed by allele-specific oligonucleotide quantitative polymerase chain reaction. Between 14 October 2015 and 29 May 2018, 48 patients were enrolled. No dose-limiting toxicity was reported, and venetoclax at 400 mg per day was chosen for extension. Eighteen (75%) relapsed and 8 (53%) untreated patients experienced grade 3/4 adverse events. The complete response rate assessed by positron emission tomography at the end of cycle 6 was 67% in relapsed and 86.6% in untreated patients. MRD clearance for evaluable patients was seen in 71.5% of relapsed (10/14 patients) and 100% of untreated MRD-evaluable patients (n = 12) at the end of 3 cycles. The median follow-up for relapsed patients was 17 months (range, 10-35 months). The 2-year progression-free survival (PFS) was 69.5% (95% confidence interval [CI], 52.9%-91.4%) and 68.6% (95% CI, 49.5%-95.1%) for overall survival. The median follow-up was 14 months (range, 5-19) for untreated patients, the 1-year PFS was 93.3% (95% CI, 81.5%-100%). The combination of obinutuzumab, ibrutinib, and venetoclax is well tolerated and provides high response rates, including at the molecular level, in relapsed and untreated MCL patients. This trial was registered at www.clinicaltrials.gov as #NCT02558816.
依鲁替尼、奥滨尤妥珠单抗和维奈托克在套细胞淋巴瘤(MCL)的临床前模型中显示出协同作用。OAsIs(NCT02558816)是一项单臂多中心前瞻性 1/2 期试验,旨在确定复发 MCL 患者中维奈托克联合固定剂量依鲁替尼和奥滨尤妥珠单抗的最大耐受剂量。在维奈托克最大耐受剂量时,为复发和未治疗患者开放了扩展队列。安全性和疗效是次要目标。微小残留病(MRD)通过等位基因特异性寡核苷酸定量聚合酶链反应进行评估。在 2015 年 10 月 14 日至 2018 年 5 月 29 日期间,共纳入 48 例患者。未报告剂量限制性毒性,选择维奈托克 400mg/天进行扩展。18 例(75%)复发和 8 例(53%)未治疗患者发生 3/4 级不良事件。在 6 个周期结束时,根据正电子发射断层扫描评估的完全缓解率在复发患者中为 67%,在未治疗患者中为 86.6%。在可评估患者中,在 3 个周期结束时,71.5%(14 例中的 10 例)的复发患者和 100%的可评估 MRD 的未治疗患者(n=12)达到 MRD 清除。复发患者的中位随访时间为 17 个月(范围,10-35 个月)。2 年无进展生存率(PFS)为 69.5%(95%置信区间[CI],52.9%-91.4%)和 68.6%(95%CI,49.5%-95.1%),总生存率为 69.5%(95%CI,52.9%-91.4%)。未治疗患者的中位随访时间为 14 个月(范围,5-19 个月),1 年 PFS 为 93.3%(95%CI,81.5%-100%)。奥滨尤妥珠单抗、依鲁替尼和维奈托克的联合治疗耐受性良好,在复发和未治疗的 MCL 患者中提供了高缓解率,包括在分子水平上。该试验在 www.clinicaltrials.gov 上注册为 #NCT02558816。