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DOI 10.1016/j.cllc.2019.03.007

Медицинская библиотека · Clinical lung cancer · 2019

Efficacy and Safety of BRAF Inhibitors With or Without MEK Inhibitors in BRAF-Mutant Advanced Non-Small-Cell Lung Cancer: Findings From a Real-Life Cohort.

Dudnik Elizabeth, Bar Jair, Peled Nir, Bshara Elias, Kuznetsov Teodor, Cohen Aharon Yonathan, Shochat Tzippy, Nechushtan Hovav, Onn Amir, Agbarya Abed, Moskovitz Mor, Keren Shoshana, Popovits-Hadar Noa, Urban Damien, Mishaeli Moshe, Rabinovich Natalie Maimon, Brenner Ronen, Zer Alona, Rotem Ofer, Roisman Laila C, Wollner Mira, Israel Lung Cancer Group

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Аннотация

BACKGROUND

Real-life comparative data on BRAF inhibitors (BRAFi) and BRAFi + MEK inhibitors (MEKi) combination in BRAF-mutant (BRAFm) non-small-cell lung cancer (NSCLC) is lacking.

PATIENTS AND

METHODS

Consecutive BRAFm advanced NSCLC patients (n = 58) treated in 9 Israeli centers in 2009-2018 were identified. These were divided according to mutation subtype and treatment into groups A1 (V600E, BRAFi; n = 5), A2 (V600E, BRAFi + MEKi; n = 15), A3 (V600E, no BRAFi; n = 7), B1 (non-V600E, BRAFi ± MEKi; n = 7), and B2 (non-V600E, no BRAFi; n = 23); one patient received both BRAFi and BRAFi + MEKi. Safety, objective response rate, progression-free survival with BRAFi ± MEKi, and overall survival were assessed.

RESULTS

Objective response rate was 40%, 67%, and 33% in groups A1, A2, and B1, respectively (P = .5 for comparison between groups A1 and A2). In group B1, G469A and L597R mutations were associated with response to BRAFi + MEKi. Median progression-free survival was 1.2 months (95% confidence interval [CI], 0.5-5.3), 5.5 months (95% CI, 0.7-9.3), and 3.6 months (95% CI, 1.5-6.7) for groups A1, A2, and B1, respectively (log-rank for comparison between groups A1 and A2, P = .04). Median overall survival with BRAFi ± MEKi was 1.7 months (95% CI, 0.5-NR), 9.5 months (95% CI, 0.2-14.9), and 7.1 months (95% CI, 1.8-NR) in groups A1, A2, and B1, respectively (log-rank for comparison between groups A1 and A2, P = .6). Safety profiles differed slightly, and similar treatment discontinuation rates were observed with BRAFi and BRAFi + MEKi.

CONCLUSION

In the real-life setting, activity and safety of BRAFi + MEKi in V600E BRAFm NSCLC are comparable to those observed in prospective clinical trials; the combination of BRAFi + MEKi is superior to monotherapy with a BRAFi. Further research should be done to explore the impact of BRAFi + MEKi treatment on the natural history of BRAFm NSCLC.

Для цитирования: Dudnik Elizabeth, Bar Jair, Peled Nir, Bshara Elias, Kuznetsov Teodor, Cohen Aharon Yonathan, Shochat Tzippy, Nechushtan Hovav, Onn Amir, Agbarya Abed, Moskovitz Mor, Keren Shoshana, Popovits-Hadar Noa, Urban Damien, Mishaeli Moshe, Rabinovich Natalie Maimon, Brenner Ronen, Zer Alona, Rotem Ofer, Roisman Laila C, Wollner Mira, Israel Lung Cancer Group. Efficacy and Safety of BRAF Inhibitors With or Without MEK Inhibitors in BRAF-Mutant Advanced Non-Small-Cell Lung Cancer: Findings From a Real-Life Cohort.. Clinical lung cancer. 2019. DOI: 10.1016/j.cllc.2019.03.007.

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