BENITIONSClinical Trial Intelligence

Pembrolizumab in MarginalzoneLymphoma A MULTICENTER OPEN LABEL SINGLE-ARM PHASE II STUDY

2期 提前终止 NCT04268277

适应症Marginal Zone Lymphoma
分期2期
申办方University of Ulm
状态提前终止
受试者人数22 人
干预(药物)Rituximab, Pembrolizumab
开始日期2022年3月1日
完成日期2024年12月6日
结果公布日2026年2月27日

摘要

For marginal zone lymphoma (MZL) Rituximab in combination with conventional chemotherapy is widely used for those patients who fail local therapy or do not qualify for such. Depending on the MZL subtype Rituximab/chemotherapy is able to induce in part long remissions, but does not prevent relapse later on. In addition, chemotherapy associated toxicity is often problematic in MZL patients, who are mostly of advanced age. Thus, chemotherapy-free approaches are highly attractive for this patient group. Rituximab single agent is a widely used chemotherapy-free approach in MZL, but was significantly inferior compared to Rituximab/chlorambucil in a large randomized prospective clinical trial in treatment naïve MZL with a CR rate of 55.8% vs. 78.8%, respectively (P \< 0.001). Thus, it is the major aim to develop chemotherapy-free approaches for MZL, which approach or surpass efficacy of rituximab/chemotherapy combinations, but avoid chemotherapy associated toxicities. Checkpoint inhibitors such as Pembrolizumab have revolutionized cancer treatment and have also shown first encouraging results in Non-Hodgkin lymphomas. Based on these observations it is the aim of this study to test the tox

CR Rate

4 weeks after end of treatment (18 cycles), approx. 58 weeks · Participants

Rituximab & Pembrolizumab3 Participants
p-value1.0
CRR value14

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