Olaparib with or without bevacizumab or bevacizumab and 5-fluorouracil in advanced colorectal cancer: Phase III LYNK-003

Author:

Kim Tae Won1ORCID,Taieb Julien2ORCID,Gurary Ellen B3ORCID,Lerman Nati3ORCID,Cui Karen4ORCID,Yoshino Takayuki5ORCID

Affiliation:

1. Department of Oncology, Asan Medical Center, University of Ulsan, Seoul 05505, South Korea

2. Georges Pompidou European Hospital, SIRIC-CARPEM, Université de Paris, Paris 75015, France

3. Oncology Late Stage Development, Merck & Co., Inc., Kenilworth, NJ 07033, USA

4. Late Development Oncology, Oncology R&D, AstraZeneca, Gaithersburg, MD 20878, USA

5. Department of Gastrointestinal Medicine, National Cancer Center Hospital East, Kashiwa 277-8577, Japan

Abstract

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. Clinical trial registration: NCT04456699

Funder

AstraZeneca

Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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