Department of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Comprehensive Cancer Center Ulm, Institute of Experimental Cancer Research, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
BMC Cancer. 2021 Jun 29;21(1):749. doi: 10.1186/s12885-021-08464-6.
Advanced stage marginal zone lymphoma (MZL) is an incurable indolent B-cell lymphoma, for which a wide variety of treatments ranging from single agent rituximab to more dose intense immunochemotherapy exists. One of the major goals in this palliative setting is to develop chemotherapy-free treatments, which approach the efficacy of immunochemotherapies, but avoid chemotherapy associated toxicity in this often elderly patient population. The PI3K inhibitor copanlisib has recently shown remarkable clinical activity in refractory or relapsed indolent B-cell lymphomas, among them MZL. Based on these data, copanlisib monotherapy was granted breakthrough designation by the FDA for the treatment of adult patients with relapsed marginal zone lymphoma who have received at least two prior therapies. However, data are still limited in particular for MZL. Based on this, the COUP-1 trial aims at testing the toxicity and efficacy of copanlisib in combination with rituximab in treatment naive and relapsed MZL.
COUP-1 is a prospective, multicenter, single-arm, open-label, non-randomized phase II trial of 6 cycles (28 days cycle) of copanlisib (60 mg intravenous day 1, 8, 15) and rituximab (375 mg/m intravenous day 1) in the induction phase followed by a maintenance phase of copanlisib (d1, d15 every 4 weeks for a maximum of 12 cycles) and rituximab (d1 every 8 weeks for a maximum of 12 cycles) in patients aged ≥18 years with previously untreated or relapsed MZL in need of treatment. A total of 56 patients are to be enrolled. Primary endpoint is the complete response (CR) rate determined 12 months after start of induction therapy. Secondary endpoints include the overall response (OR) rate, progression free survival (PFS), overall survival (OS), safety and patient related outcome with quality of life. The study includes a translational bio-sampling program with the prospect to measure minimal residual disease. The study was initiated in November 2019.
The COUP-1 trial evaluates the efficacy and toxicity of the treatment of copanlisib in combination with rituximab in patients with MZL and additionally offers the chance for translational research in this heterogenous type of lymphoma.
ClinicalTrials.gov : NCT03474744 . Registration date: 03/23/2018.
晚期边缘区淋巴瘤(MZL)是一种无法治愈的惰性 B 细胞淋巴瘤,对于这种疾病,存在各种治疗方法,从单一药物利妥昔单抗到更强化的免疫化疗都有。在这种姑息治疗环境下,一个主要目标是开发无化疗治疗方法,这些方法在疗效上可与免疫化疗相当,但在这类常为老年患者人群中避免化疗相关毒性。PI3K 抑制剂 copanlisib 最近在复发性或难治性惰性 B 细胞淋巴瘤中显示出显著的临床活性,其中包括 MZL。基于这些数据,copanlisib 单药治疗被 FDA 授予突破性指定,用于治疗至少接受过两种先前治疗的复发性边缘区淋巴瘤成年患者。然而,目前数据在 MZL 方面仍然有限。基于此,COUP-1 试验旨在测试 copanlisib 联合利妥昔单抗在初治和复发性 MZL 中的毒性和疗效。
COUP-1 是一项前瞻性、多中心、单臂、开放标签、非随机的 II 期试验,共 6 个周期(28 天周期),在诱导期给予 copanlisib(60mg 静脉注射,第 1、8、15 天)和利妥昔单抗(375mg/m 静脉注射,第 1 天),随后给予 copanlisib(d1、d15,每 4 周一次,最多 12 个周期)和利妥昔单抗(d1,每 8 周一次,最多 12 个周期)维持治疗,入组年龄≥18 岁、未经治疗或复发需要治疗的 MZL 患者。共计划入组 56 例患者。主要终点是诱导治疗开始后 12 个月确定的完全缓解(CR)率。次要终点包括总缓解(OR)率、无进展生存期(PFS)、总生存期(OS)、安全性和患者相关结局(生活质量)。该研究包括一个转化生物样本采集计划,有机会测量微小残留疾病。该研究于 2019 年 11 月启动。
COUP-1 试验评估了 copanlisib 联合利妥昔单抗治疗 MZL 患者的疗效和毒性,此外还为这种异质性淋巴瘤类型的转化研究提供了机会。
ClinicalTrials.gov:NCT03474744。注册日期:2018 年 3 月 23 日。