Swalduz Aurélie, Beau-Faller Michèle, Planchard David, Mazieres Julien, Bayle-Bleuez Sophie, Debieuvre Didier, Fallet Vincent, Geier Margaux, Cortot Alexis, Couraud Sébastien, Daniel Catherine, Domblides Charlotte, Pichon Eric, Fabre Elizabeth, Larivé Sébastien, Lerolle Ulrike, Tomasini Pascale, Wislez Marie, Missy Pascale, Morin Franck, Westeel Virginie, Auliac Jean-Bernard
Centre Léon Bérard, Department of Medical Oncology, Lyon, France.
Centre Hospitalier Universitaire Strasbourg, Laboratoire d'Onco-Biologie & Oncologie Thoracique Hôpital de Hautepierre & Nouvel Hôpital Civil, INSERM UMR 1260 - Nanomédecine Régénérative, Université de Strasbourg - CRBS, Strasbourg, France.
Lung Cancer. 2025 Jan;199:108038. doi: 10.1016/j.lungcan.2024.108038. Epub 2024 Nov 26.
BRAF V600E mutations occur in 2-5 % of advanced non-small cell lung cancer (NSCLC) patients. The dabrafenib-trametinib (D-T) combination was associated with improved and durable OS in patients in phase II. This study (IFCT-2004 BLaDE study) reported the efficacy of D-T combination in a large retrospective French real-world multicenter cohort of patients with advanced BRAF V600E-mutated NSCLC.
Patients with advanced BRAF V600E-mutated NSCLC diagnosed between 01.01.2016 and 31.12.2019 and treated with D-T in combination, regardless of the treatment line, were included. The primary endpoint was the 12-month OS rate (%) in patients receiving D-T as a second-line therapy or beyond.
A total of 163 patients were included: 50.3 % were female, 30.2 % were never smokers, 95.1 % had adenocarcinoma, and 78.2 % had a PDL1 ≥ 1 %. The median age was 68.3 years. At D-T initiation, 80.8 % of patients had a PS of 0/1, 78.6 % had stage IV disease, and 20.9 % had brain metastasis. At the cutoff, the median follow-up was 27.4 months. The 12-month OS rate in patients receiving D + T as a second-line therapy or beyond (n = 119) was 67.4 %, with a median progression-free survival (mPFS) of 10.4 months. Among the 44 patients who received D + T as a first-line therapy, the 12-month OS rate was 67.4 %, with an mPFS of 18.2 months. D-T discontinuation for toxicity was reported in 10.3 % of patients.
To our knowledge, this is the largest retrospective cohort of BRAF-mutated patients reported. The findings confirmed the significant efficacy of D-T in combination with BRAF V600E-mutated metastatic NSCLC in pretreated and untreated patients. These results under real-world conditions are consistent with those of other registered studies.
BRAF V600E 突变发生在 2%-5% 的晚期非小细胞肺癌(NSCLC)患者中。在 II 期研究中,达拉非尼-曲美替尼(D-T)联合用药可改善并延长患者的总生存期(OS)。本研究(IFCT-2004 BLaDE 研究)报告了 D-T 联合用药在法国一项大型回顾性真实世界多中心队列中的疗效,该队列中的患者均为晚期 BRAF V600E 突变的 NSCLC 患者。
纳入 2016 年 1 月 1 日至 2019 年 12 月 31 日期间诊断为晚期 BRAF V600E 突变 NSCLC 并接受 D-T 联合治疗的患者,无论其治疗线数。主要终点是接受 D-T 作为二线或更后线治疗的患者的 12 个月总生存率(%)。
共纳入 163 例患者:50.3% 为女性,30.2% 为从不吸烟者,95.1% 患有腺癌,78.2% 的患者程序性死亡受体 1(PDL1)≥1%(译者注:原文中 “PDL1” 有误,应为 “PD-L1”)。中位年龄为 68.3 岁。开始使用 D-T 时,80.8% 的患者体力状况(PS)评分为 0/1,78.6% 为 IV 期疾病,20.9% 有脑转移。截至分析时,中位随访时间为 27.4 个月。接受 D+T 作为二线或更后线治疗的患者(n = 119)的 12 个月总生存率为 67.4%,中位无进展生存期(mPFS)为 10.4 个月。在 44 例接受 D+T 作为一线治疗的患者中,12 个月总生存率为 67.4%,mPFS 为 18.2 个月。10.3% 的患者报告因毒性而停用 D-T。
据我们所知,这是报告的最大规模的 BRAF 突变患者回顾性队列。研究结果证实了 D-T 联合用药对 BRAF V600E 突变的转移性 NSCLC 患者(无论是否接受过治疗)具有显著疗效。这些真实世界条件下的结果与其他注册研究的结果一致。