Department of Medical Oncology, La Paz University Hospital, Paseo de la castellana 261, 28046, Madrid, Spain.
Clin Transl Oncol. 2019 Aug;21(8):1061-1066. doi: 10.1007/s12094-018-02028-0. Epub 2019 Jan 3.
The treatment of patients with BRAFv600 mutant melanomas progressing to BRAF inhibitors (BRAFi) and immunotherapy remains challenging. Preclinical studies and a small phase 2 trials have recently suggested that rechallenging with BRAFi may have a roll in these patients. The aim of this systematic review was to summarise the current evidence on the efficacy of BRAF inhibition therapy rechallenge after progression to BRAFi in metastatic BRAFv600 melanoma patients.
We performed a systematic literature search in MEDLINE, Embase and the Cochrane Library CENTRAL up to November 2018. The target was restricted to patients with unresectable and/or metastatic BRAF V600 mutant melanoma that had previously progressed on BRAFi, were off-treatment for a period of time and then retreated with a BRAF inhibition strategy. We included prospective trials, observational studies and case reports. The primary outcomes were overall response rate (ORR), disease control rate (DCR), median progression-free survival (PFS) and median overall survival since the start of the treatment.
Up to November 2018, nine reports met our inclusion criteria: five case reports, three observational studies and a phase 2 trial. No comparative studies have been reported. In total, 188 patients met the inclusion criteria for this review. Efficacy results of the observational reports and the clinical trial are presented. ORR varied between 28 and 43% and DCR between 57 and 72%. Duration of response was reported in 1 retrospective study and was of 14 months. PFS varied between 4.9 and 5 months and OS was not reported in all studies.
Although no comparative studies have been conducted, rechallenging with BRAF inhibition therapy seems a plausible treatment option. Randomized trials are needed to confirm these results.
BRAFv600 突变黑色素瘤患者在进展至 BRAF 抑制剂(BRAFi)和免疫治疗后,其治疗仍然具有挑战性。最近的临床前研究和小型 2 期试验表明,重新使用 BRAFi 可能对这些患者有效。本系统评价的目的是总结目前关于 BRAFv600 突变黑色素瘤患者在进展至 BRAFi 后重新使用 BRAF 抑制治疗的疗效证据。
我们在 MEDLINE、Embase 和 Cochrane 图书馆 CENTRAL 中进行了系统的文献检索,检索时间截至 2018 年 11 月。目标人群为先前接受过 BRAFi 治疗、进展后停药一段时间、然后重新使用 BRAF 抑制策略的不可切除和/或转移性 BRAF V600 突变黑色素瘤患者。我们纳入了前瞻性试验、观察性研究和病例报告。主要结局指标是总缓解率(ORR)、疾病控制率(DCR)、中位无进展生存期(PFS)和治疗开始后的中位总生存期。
截至 2018 年 11 月,有 9 份报告符合我们的纳入标准:5 份病例报告、3 份观察性研究和 1 项 2 期试验。没有报告比较性研究。共有 188 名患者符合本综述的纳入标准。我们呈现了观察性报告和临床试验的疗效结果。ORR 范围为 28%至 43%,DCR 范围为 57%至 72%。1 项回顾性研究报告了缓解持续时间,为 14 个月。PFS 范围为 4.9 至 5 个月,所有研究均未报告 OS。
尽管没有进行比较性研究,但重新使用 BRAF 抑制治疗似乎是一种合理的治疗选择。需要进行随机试验来证实这些结果。