Long G V, Flaherty K T, Stroyakovskiy D, Gogas H, Levchenko E, de Braud F, Larkin J, Garbe C, Jouary T, Hauschild A, Chiarion-Sileni V, Lebbe C, Mandalà M, Millward M, Arance A, Bondarenko I, Haanen J B A G, Hansson J, Utikal J, Ferraresi V, Mohr P, Probachai V, Schadendorf D, Nathan P, Robert C, Ribas A, Davies M A, Lane S R, Legos J J, Mookerjee B, Grob J-J
Melanoma Institute Australia, The University of Sydney, and Royal North Shore and Mater Hospitals, North Sydney, Australia.
Developmental Therapeutics and Melanoma Programs, Massachusetts General Hospital Cancer Center, Boston, USA.
Ann Oncol. 2017 Jul 1;28(7):1631-1639. doi: 10.1093/annonc/mdx176.
Previous analysis of COMBI-d (NCT01584648) demonstrated improved progression-free survival (PFS) and overall survival (OS) with combination dabrafenib and trametinib versus dabrafenib monotherapy in BRAF V600E/K-mutant metastatic melanoma. This study was continued to assess 3-year landmark efficacy and safety after ≥36-month follow-up for all living patients.
This double-blind, phase 3 study enrolled previously untreated patients with BRAF V600E/K-mutant unresectable stage IIIC or stage IV melanoma. Patients were randomized to receive dabrafenib (150 mg twice daily) plus trametinib (2 mg once daily) or dabrafenib plus placebo. The primary endpoint was PFS; secondary endpoints were OS, overall response, duration of response, safety, and pharmacokinetics.
Between 4 May and 30 November 2012, a total of 423 of 947 screened patients were randomly assigned to receive dabrafenib plus trametinib (n = 211) or dabrafenib monotherapy (n = 212). At data cut-off (15 February 2016), outcomes remained superior with the combination: 3-year PFS was 22% with dabrafenib plus trametinib versus 12% with monotherapy, and 3-year OS was 44% versus 32%, respectively. Twenty-five patients receiving monotherapy crossed over to combination therapy, with continued follow-up under the monotherapy arm (per intent-to-treat principle). Of combination-arm patients alive at 3 years, 58% remained on dabrafenib plus trametinib. Three-year OS with the combination reached 62% in the most favourable subgroup (normal lactate dehydrogenase and <3 organ sites with metastasis) versus only 25% in the unfavourable subgroup (elevated lactate dehydrogenase). The dabrafenib plus trametinib safety profile was consistent with previous clinical trial observations, and no new safety signals were detected with long-term use.
These data demonstrate that durable (≥3 years) survival is achievable with dabrafenib plus trametinib in patients with BRAF V600-mutant metastatic melanoma and support long-term first-line use of the combination in this setting.
之前对COMBI-d(NCT01584648)的分析表明,与达拉非尼单药治疗相比,达拉非尼联合曲美替尼治疗BRAF V600E/K突变型转移性黑色素瘤可改善无进展生存期(PFS)和总生存期(OS)。本研究继续进行,以评估所有存活患者在随访≥36个月后的3年标志性疗效和安全性。
这项双盲3期研究纳入了先前未接受过治疗的BRAF V600E/K突变型不可切除的IIIC期或IV期黑色素瘤患者。患者被随机分配接受达拉非尼(每日两次,每次150mg)联合曲美替尼(每日一次,每次2mg)或达拉非尼联合安慰剂。主要终点为PFS;次要终点为OS、总体缓解率、缓解持续时间、安全性和药代动力学。
在2012年5月4日至11月30日期间,947例筛查患者中的423例被随机分配接受达拉非尼联合曲美替尼(n = 211)或达拉非尼单药治疗(n = 212)。在数据截止时(2016年2月15日),联合治疗的疗效仍然更佳:达拉非尼联合曲美替尼的3年PFS为22%,而单药治疗为12%,3年OS分别为44%和32%。25例接受单药治疗的患者交叉接受联合治疗,并在单药治疗组继续随访(根据意向性分析原则)。在联合治疗组中存活3年的患者中,58%仍在接受达拉非尼联合曲美替尼治疗。在最有利的亚组(乳酸脱氢酶正常且转移器官部位<3个)中,联合治疗的3年OS达到62%,而在不利亚组(乳酸脱氢酶升高)中仅为25%。达拉非尼联合曲美替尼的安全性与之前的临床试验观察结果一致,长期使用未发现新的安全信号。
这些数据表明,BRAF V600突变型转移性黑色素瘤患者使用达拉非尼联合曲美替尼可实现持久(≥3年)生存,并支持在此情况下长期一线使用该联合方案。