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.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] Trifluridine/tipiracil plus bevacizumab as a first-line treatment for elderly patients with metastatic colorectal cancer (KSCC1602): A multicenter phase II trial
    Oki, Eiji
    Makiyama, Akitaka
    Miyamoto, Yuji
    Kotaka, Masahiko
    Kawanaka, Hirofumi
    Miwa, Keisuke
    Kabashima, Akira
    Noguchi, Tomohiro
    Yuge, Kotaro
    Kashiwada, Tomomi
    Ando, Koji
    Shimokawa, Mototsugu
    Saeki, Hiroshi
    Akagi, Yoshito
    Baba, Hideo
    Maehara, Yoshihiko
    Mori, Masaki
    CANCER MEDICINE, 2021, 10 (02): : 454 - 461
  • [32] Trifluridine/tipiracil plus bevacizumab in elderly patients with previously untreated metastatic colorectal cancer (KSCC1602): A multicenter, phase II clinical trial.
    Oki, Eiji
    Makiyama, Akitaka
    Miyamoto, Yuji
    Kotaka, Masahito
    Kawanaka, Hirofumi
    Miwa, Keisuke
    Kabashima, Akira
    Hamanoue, Masahiro
    Ohchi, Takafumi
    Kashiwada, Tomomi
    Shimokawa, Mototsugu
    Saeki, Hiroshi
    Akagi, Yoshito
    Baba, Hideo
    Mori, Masaki
    JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (15)
  • [33] Overall survival results from a phase III trial of trifluridine/tipiracil versus placebo in patients with metastatic gastric cancer refractory to standard therapies (TAGS)
    Tabernero, J.
    Shitara, K.
    Dvorkin, M.
    Mansoor, W.
    Arkenau, H. T.
    Prokharau, A.
    Alsina, M.
    Ghidini, M.
    Faustino, C.
    Gorbunova, V.
    Zhavrid, E.
    Nishikawa, K.
    Hosokawa, A.
    Ganea, D.
    Yalcin, S.
    Fujitani, K.
    Beretta, G.
    Winkler, R.
    Makris, L.
    Doi, T.
    Ilson, D.
    ANNALS OF ONCOLOGY, 2018, 29 : 122 - 122
  • [34] A phase 2 trial of trifluridine/tipiracil plus nivolumab in patients with heavily pretreated microsatellite-stable metastatic colorectal cancer
    Patel, Manish R.
    Falchook, Gerald S.
    Hamada, Kensuke
    Makris, Lukas
    Bendell, Johanna C.
    CANCER MEDICINE, 2021, 10 (04): : 1183 - 1190
  • [35] Predicting Trifluridine/Tipiracil Treatment Outcomes in Refractory Metastatic Colorectal Cancer Patients: A Multicenter Exploratory Analysis
    Prejac, Juraj
    Omcen, Tomislav
    Radic, Jasna
    Vrdoljak, Eduard
    Frobe, Ana
    Plestina, Stjepko
    ONCOLOGY, 2024, 102 (03) : 217 - 227
  • [36] Pooled safety analysis from phase III studies of trifluridine/tipiracil in patients with metastatic gastric or gastroesophageal junction cancer and metastatic colorectal cancer
    Van Cutsem, E.
    Hochster, H.
    Shitara, K.
    Mayer, R.
    Ohtsu, A.
    Falcone, A.
    Yoshino, T.
    Doi, T.
    Ilson, D. H.
    Arkenau, H-T
    George, B.
    Benhadji, K. A.
    Makris, L.
    Tabernero, J.
    ESMO OPEN, 2022, 7 (06)
  • [37] Lonsurf (trifluridine/tipiracil): Assessing the impact of dose related toxicities and progression free survival in (refractory) metastatic colorectal cancer
    Court, Olivia R.
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2022, 28 (05) : 1085 - 1092
  • [38] Survival analysis based on the grade of neutropenia in patients with metastatic colorectal cancer treated with trifluridine-tipiracil
    Avino Tarazona, V.
    Rodriguez Garces, M.
    Amor Urbano, M.
    Bolanos Naranjo, M.
    ANNALS OF ONCOLOGY, 2021, 32 : S140 - S140
  • [39] Trifluridine/Tipiracil Plus Bevacizumab for Vulnerable Patients With Pretreated Metastatic Colorectal Cancer: A Retrospective Study (WJOG14520G)
    Kito, Yosuke
    Kawakami, Hisato
    Mitani, Seiichiro
    Nishina, Shinichi
    Matsumoto, Toshihiko
    Tsuzuki, Takao
    Shinohara, Yudai
    Shimokawa, Hozumi
    Kumanishi, Ryosuke
    Ohta, Takashi
    Katsuya, Hiroo
    Kawakami, Takeshi
    Nishina, Tomohiro
    Hasegawa, Hiroko
    Akiyoshi, Kohei
    Chiba, Yasutaka
    Yamazaki, Kentaro
    Hironaka, Shuichi
    Muro, Kei
    ONCOLOGIST, 2024, 29 (03): : E330 - E336
  • [40] Association between sidedness and survival among chemotherapy refractory metastatic colorectal cancer patients treated with trifluridine/tipiracil or regorafenib
    Hsiao, Kai-Yuan
    Chen, Hsin-Pao
    Rau, Kun-Ming
    Liu, Kuang-Wen
    Shia, Ben-Chang
    Chang, Wei-Shan
    Liang, Hao-Yun
    Hsieh, Meng-Che
    ONCOLOGIST, 2024,