Department of Investigational Cancer Therapeutics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Mol Cancer. 2024 Mar 26;23(1):64. doi: 10.1186/s12943-024-01982-4.
Previous studies have shown the clinical benefit of rechallenging the RAF pathway in melanoma patients previously treated with BRAF inhibitors. 44 patients with multiple tumors harboring RAF alterations were rechallenged with a second RAF inhibitor, either as monotherapy or in combination with other therapies, after prior therapy with a first RAF inhibitor. This retrospective observational study results showed that rechallenging with RAFi(s) led to an overall response rate of 18.1% [PR in thyroid (1 anaplastic; 3 papillary), 1 ovarian, 2 melanoma, 1 cholangiocarcinoma, and 1 anaplastic astrocytoma]. The clinical benefit rate was 54.5%; more than 30% of patients had durable responses with PR and SD lasting > 6 months. The median progression-free survival on therapy with second RAF inhibitor in the rechallenge setting either as monotherapy or combination was shorter at 2.7 months (0.9-30.1 m) compared to 8.6 months (6.5-11.5 m) with RAF-1i. However, the median PFS with RAF-2i responders (PFS-2) improved at 12.8 months compared to 11.4 months with RAF-1i responders. The median OS from retreatment with RAF-2i was 15.5 months (11.1-30.8 m). Further prospective studies are needed to validate these results and expand targeted therapy options for RAF-aberrant cancers.
先前的研究表明,在先前接受 BRAF 抑制剂治疗的黑色素瘤患者中重新挑战 RAF 通路具有临床获益。44 例携带 RAF 改变的多灶肿瘤患者在先前接受 BRAF 抑制剂治疗后,接受了第二种 RAF 抑制剂的再次挑战,包括单药治疗或联合其他疗法。这项回顾性观察性研究结果表明,重新挑战 RAFi(s)导致总体缓解率为 18.1%[甲状腺(1 例间变性;3 例乳头状)、1 例卵巢、2 例黑色素瘤、1 例胆管癌和 1 例间变性星形细胞瘤的 PR]。临床获益率为 54.5%;超过 30%的患者有持久的反应,PR 和 SD 持续时间超过 6 个月。在再次挑战设置中,第二种 RAF 抑制剂单药或联合治疗的中位无进展生存期为 2.7 个月(0.9-30.1 m),明显短于 RAF-1i 的 8.6 个月(6.5-11.5 m)。然而, RAF-2i 应答者的中位 PFS(PFS-2)改善至 12.8 个月,而 RAF-1i 应答者为 11.4 个月。从 RAF-2i 再次治疗的中位 OS 为 15.5 个月(11.1-30.8 m)。需要进一步的前瞻性研究来验证这些结果,并扩大 RAF 异常癌症的靶向治疗选择。