Impact of KRAS G12 mutations on survival with trifluridine/tipiracil plus bevacizumab in patients with refractory metastatic colorectal cancer: post hoc analysis of the phase III SUNLIGHT trial ☆
ESMO Open, ISSN: 2059-7029, Vol: 9, Issue: 3, Page: 102945
2024
- 3Citations
- 13Captures
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- Citations3
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- 13
Article Description
In metastatic colorectal cancer (mCRC), KRAS mutations are often associated with poorer survival; however, the prognostic impact of specific point mutations is unclear. In the phase III SUNLIGHT trial, trifluridine/tipiracil (FTD/TPI) plus bevacizumab significantly improved overall survival (OS) versus FTD/TPI alone. We assessed the impact of KRAS G12 mutational status on OS in SUNLIGHT. In the global, open-label, randomized, phase III SUNLIGHT trial, adults with mCRC who had received no more than two prior chemotherapy regimens were randomized 1 : 1 to receive FTD/TPI alone or FTD/TPI plus bevacizumab. In this post hoc analysis, OS was assessed according to the presence or absence of a KRAS G12 mutation in the overall population and in patients with RAS -mutated tumors. Overall, 450 patients were analyzed, including 302 patients in the RAS mutation subgroup (214 with a KRAS G12 mutation and 88 with a non- KRAS G12 RAS mutation). In the overall population, similar OS outcomes were observed in patients with and without a KRAS G12 mutation [median 8.3 and 9.2 months, respectively; hazard ratio (HR) 1.09, 95% confidence interval (CI) 0.87-1.4]. Similar OS outcomes were also observed in the subgroup analysis of patients with a KRAS G12 mutation versus those with a non- KRAS G12 RAS mutation (HR 1.03, 95% CI 0.76-1.4). FTD/TPI plus bevacizumab improved OS compared with FTD/TPI alone irrespective of KRAS G12 mutational status. Among patients with a KRAS G12 mutation, the median OS was 9.4 months with FTD/TPI plus bevacizumab versus 7.2 months with FTD/TPI alone (HR 0.67, 95% CI 0.48-0.93), and in patients without a KRAS G12 mutation, the median OS was 11.3 versus 7.1 months, respectively (HR 0.59, 95% CI 0.43-0.81). The presence of a KRAS G12 mutation had no detrimental effect on OS among patients treated in SUNLIGHT. The benefit of FTD/TPI plus bevacizumab over FTD/TPI alone was confirmed independently of KRAS G12 status.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2059702924007130; http://dx.doi.org/10.1016/j.esmoop.2024.102945; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85187358653&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38471240; https://linkinghub.elsevier.com/retrieve/pii/S2059702924007130; https://dx.doi.org/10.1016/j.esmoop.2024.102945
Elsevier BV
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