Department of Oncology, Asan Medical Center, University of Ulsan, Seoul 05505, South Korea.
Georges Pompidou European Hospital, SIRIC-CARPEM, Université de Paris, Paris 75015, France.
Future Oncol. 2021 Dec;17(36):5013-5022. doi: 10.2217/fon-2021-0899. Epub 2021 Nov 15.
Oxaliplatin-based chemotherapy with a regimen such as FOLFOX with or without targeted therapy is a standard of care option for advanced colorectal cancer; however, long-term exposure to oxaliplatin is associated with cumulative toxicity. Growing evidence suggests maintenance therapy with a less intensive regimen after platinum-based induction therapy can provide continuing benefit with reduced toxicity. We describe the rationale and design of the Phase III LYNK-003 trial, which will evaluate the efficacy and safety of olaparib with or without bevacizumab compared with 5-fluoruracil plus bevacizumab in patients with unresectable or metastatic colorectal cancer that has not progressed on an induction course of FOLFOX plus bevacizumab. The primary end point is progression-free survival by independent central review; secondary end points include overall survival, objective response, duration of response and safety. NCT04456699.
奥沙利铂为基础的化疗方案,如 FOLFOX 联合或不联合靶向治疗,是晚期结直肠癌的标准治疗选择;然而,长期接触奥沙利铂与累积毒性有关。越来越多的证据表明,在铂类诱导治疗后使用强度较低的维持治疗可以在降低毒性的同时提供持续的益处。我们描述了 III 期 LYNK-003 试验的原理和设计,该试验将评估奥拉帕利联合或不联合贝伐珠单抗与 5-氟尿嘧啶联合贝伐珠单抗在接受 FOLFOX 联合贝伐珠单抗诱导治疗后疾病未进展的不可切除或转移性结直肠癌患者中的疗效和安全性。主要终点是独立中心审查的无进展生存期;次要终点包括总生存期、客观缓解率、缓解持续时间和安全性。NCT04456699。