Impact of KRASG12 mutations on survival with trifluridine/tipiracil plus bevacizumab in patients with refractory metastatic colorectal cancer: post hoc analysis of the phase III SUNLIGHT trial

被引:2
|
作者
Tabernero, J. [1 ,12 ]
Taieb, J. [2 ]
Fakih, M. [3 ]
Prager, G. W. [4 ]
Van Cutsem, E. [5 ,6 ]
Ciardiello, F. [7 ]
Mayer, R. J. [8 ]
Amellal, N. [9 ]
Skanji, D. [9 ]
Calleja, E. [10 ]
Yoshino, T. [11 ]
机构
[1] Vall dHebron Inst Oncol VHIO, Vall dHebron Hosp Campus, Barcelona, Spain
[2] Paris Cite Univ, Georges Pompidou European Hosp, AP HP, SIR CARPEM Comprehens Canc Ctr, Paris, France
[3] City Hope Comprehens Canc Ctr, Duarte, CA USA
[4] Med Univ Vienna, Dept Med 1, Vienna, Austria
[5] Univ Hosp Gasthuisberg, Leuven, Belgium
[6] Katholieke Univ Leuven, Leuven, Belgium
[7] Univ Campania Luigi Vanvitelli, Naples, Italy
[8] Dana Farber Canc Inst, Boston, MA USA
[9] Servier Int Res Inst, Suresnes, France
[10] Taiho Oncol Inc, Princeton, NJ USA
[11] Natl Canc Ctr Hosp East, Kashiwa, Japan
[12] Vall dHebron Inst Oncol VHIO, Vall dHebron Hosp Campus, Med Oncol Dept, P Vall dHebron 119-129, Barcelona 08035, Spain
关键词
bevacizumab; KRAS mutation; metastatic colorectal cancer; overall survival; phase III; trifluridine/tipiracil; RAS MUTATIONS; TAS-102; ASSOCIATION; CETUXIMAB; THERAPY;
D O I
10.1016/j.esmoop.2024.102945
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: 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 KRASG12 mutational status on OS in SUNLIGHT. Patients and methods: 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 KRASG12 mutation in the overall population and in patients with RAS-mutated tumors. Results: Overall, 450 patients were analyzed, including 302 patients in the RAS mutation subgroup (214 with a KRASG12 mutation and 88 with a non-KRASG12 RAS mutation). In the overall population, similar OS outcomes were observed in patients with and without a KRASG12 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 KRASG12 mutation versus those with a non-KRASG12 RAS mutation (HR 1.03, 95% CI 0.76-1.4). FTD/TPI plus bevacizumab improved OS compared with FTD/TPI alone irrespective of KRASG12 mutational status. Among patients with a KRASG12 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 KRASG12 mutation, the median OS was 11.3 versus 7.1 months, respectively (HR 0.59, 95% CI 0.43-0.81). Conclusions: The presence of a KRASG12 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 KRASG12 status.
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页数:8
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