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A phase II study of the PI3K inhibitor copanlisib in combination with the anti-CD20 monoclonal antibody rituximab for patients with marginal zone lymphoma: treatment rationale and protocol design of the COUP-1 trial

机译:PI3K抑制剂Copanlisib与抗CD20单克隆抗体Rituximab与边缘区淋巴瘤患者组合的II期研究:治疗理论和协议设计的COUP-1试验

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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/m2 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.
机译:先进的阶段边缘区淋巴瘤(MZL)是一种可治区惰性的B细胞淋巴瘤,其中各种各样的处理从单粒rituximab到更多剂量强烈的免疫化学疗法。这种姑息地区的主要目标之一是开发无疗法的免疫疗法治疗,避免在这种经常老年患者人群中进行化疗相关的毒性。 PI3K抑制剂Copanlisib最近在难敏或复发的惰性B细胞淋巴瘤中显示出显着的临床活性,其中MZL。基于这些数据,Copanlisib单疗法被FDA授予突破性指定用于治疗成年患者,该患者已经收到至少两个先前疗法。然而,数据仍然有限于MZL。基于此,COUP-1试验旨在测试Copanlisib与Rituximab在治疗Naive和复发后的MZL中的毒性和功效。 COUP-1是一种前瞻性,多中心,单臂,开放标签,非随机化第二次试验6?循环(28?天?循环)的Copanlisib(60?Mg静脉内第1,8,15)和Rituximab (375?mg / m 2静脉内第1天)在诱导阶段,然后进行Copanlisib的维持阶段(D1,D15每4?周最多为12?循环)和rituximab(每8个月,最多每8个时间为12个循环)≥18岁的患者,以前未经治疗或复发的MZL需要治疗。共有56名患者才能注册。主要终点是在感应治疗开始后12个月的完全响应(CR)速率。次要终点包括总体响应(或)率,进展免费存活(PFS),整体存活(OS),安全性和患者相关结果与生活质量。该研究包括一个平移生物抽样计划,具有措施来衡量最小的残留疾病。该研究于2019年11月开始。粮食委员会试验评估了与MZL患者的Rituximab联合治疗Copanlisib的疗效和毒性,另外为这种异质类型的淋巴瘤提供了转化研究的机会。 ClinicalTrials.gov:NCT03474744。注册日期:03/23/2018。

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