Pérol Maurice, Solomon Benjamin J, Goto Koichi, Park Keunchil, Nadal Ernest, Bria Emilio, Martin Claudio, Bar Jair, Williams Justin N, Puri Tarun, Li Jian, Uh Minji K, Lin Boris K, Zhou Caicun
Centre Léon Bérard, Lyon, France.
Peter MacCallum Cancer Institute, Melbourne, VIC, Australia.
J Clin Oncol. 2024 Jul 20;42(21):2500-2505. doi: 10.1200/JCO.24.00724. Epub 2024 Jun 3.
JCO .Although the CNS activity of selpercatinib in patients with fusion-positive non-small cell lung cancer (NSCLC) has been previously described, the ability of potent RET inhibition to prevent new CNS metastases from developing has been challenging to measure without randomized data. Serial CNS scans were studied from LIBRETTO-431, a randomized phase III trial of selpercatinib versus platinum/pemetrexed ± pembrolizumab whose primary results have been previously disclosed. Intracranial outcomes were assessed by neuroradiologic blinded independent central review in patients with baseline and ≥1 postbaseline CNS scans. Of the 192 patients within the intention-to-treat pembrolizumab population with baseline CNS scans, 150 patients were without baseline CNS metastases. The cumulative incidence of CNS progression in these patients was reduced with selpercatinib versus chemotherapy + pembrolizumab (cause-specific hazard ratio [HR], 0.17 [95% CI, 0.04 to 0.69]). The HR for intracranial progression-free survival (PFS) was 0.46 (95% CI, 0.18 to 1.18). Among the 42 patients with baseline CNS metastases, similar trends were observed in the cumulative incidence of CNS progression (cause-specific HR, 0.61 [95% CI, 0.19 to 1.92]) and intracranial PFS (HR, 0.74 [95% CI, 0.28 to 1.97]). These data demonstrate that selpercatinib effectively treats existing CNS disease and prevents or delays the formation of new CNS metastases. These results reinforce the importance of identifying fusions in first-line patients with NSCLC and treating with selpercatinib.
《临床肿瘤学杂志》。虽然先前已描述过塞尔帕替尼在融合阳性非小细胞肺癌(NSCLC)患者中的中枢神经系统活性,但在缺乏随机数据的情况下,强效RET抑制预防新的中枢神经系统转移发生的能力一直难以衡量。对LIBRETTO-431研究中的系列中枢神经系统扫描结果进行了分析,该研究是一项塞尔帕替尼对比铂类/培美曲塞±帕博利珠单抗的随机III期试验,其主要结果此前已公布。对有基线及≥1次基线后中枢神经系统扫描的患者,通过神经放射学盲法独立中央审查评估颅内结局。在意向性分析的帕博利珠单抗治疗人群中,有192例患者进行了基线中枢神经系统扫描,其中150例患者基线时无中枢神经系统转移。与化疗+帕博利珠单抗相比,塞尔帕替尼降低了这些患者中枢神经系统进展的累积发生率(病因特异性风险比[HR],0.17[95%CI,0.04至0.69])。颅内无进展生存期(PFS)的HR为0.46(95%CI,0.18至1.18)。在42例有基线中枢神经系统转移的患者中,中枢神经系统进展的累积发生率(病因特异性HR,0.61[95%CI,0.19至1.92])和颅内PFS(HR,0.74[95%CI,0.28至1.97])也观察到类似趋势。这些数据表明,塞尔帕替尼可有效治疗现有的中枢神经系统疾病,并预防或延迟新的中枢神经系统转移的形成。这些结果强化了在一线NSCLC患者中识别融合并使用塞尔帕替尼治疗的重要性。
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