Stagno Anna, Vari Sabrina, Annovazzi Alessio, Anelli Vincenzo, Russillo Michelangelo, Cognetti Francesco, Ferraresi Virginia
Department of Medical Oncology 1, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Nuclear Medicine Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Front Oncol. 2021 May 31;11:645008. doi: 10.3389/fonc.2021.645008. eCollection 2021.
The combination of BRAF and MEK inhibitors represents the standard of care treatment for patients with metastatic -mutated melanoma, notwithstanding the high frequency of emergent resistance. Moreover, therapeutic options outside clinical trials are scarce when patients have progressed after both targeted therapy and therapy with immune checkpoint inhibitors. In this article, we report our experience with targeted therapy rechallenging with BRAF and MEK inhibitors in patients with metastatic -mutated melanoma after progression with kinase inhibitors and immunotherapy.
Four patients with metastatic -mutated melanoma were rechallenged with BRAF and MEK inhibitors after progression with targeted therapy and subsequent immunotherapy (checkpoint inhibitors).
Two patients (one of them was heavily pretreated) had partial response over 36 months (with local treatment on oligoprogression disease) and 10 months, respectively. A third patient with multisite visceral disease and high serum levels of lactate dehydrogenase had a short-lived clinical benefit rapidly followed by massive progression of disease (early progressor). The fourth patient, currently on treatment with BRAF/MEK inhibitors, is showing a clinical benefit and radiological stable disease over 3 months of therapy. Adverse events were manageable, similar to those reported during the first targeted therapy; the treatment was better tolerated at rechallenge compared with the first treatment by two out of four patients.
BRAF和MEK抑制剂联合使用是转移性BRAF突变型黑色素瘤患者的标准治疗方案,尽管出现耐药的频率很高。此外,当患者在靶向治疗和免疫检查点抑制剂治疗后病情进展时,临床试验之外的治疗选择很少。在本文中,我们报告了转移性BRAF突变型黑色素瘤患者在激酶抑制剂和免疫治疗进展后,再次使用BRAF和MEK抑制剂进行靶向治疗的经验。
4例转移性BRAF突变型黑色素瘤患者在靶向治疗和随后的免疫治疗(检查点抑制剂)进展后,再次接受BRAF和MEK抑制剂治疗。
2例患者(其中1例接受过大量预处理)分别在36个月(对寡进展性疾病进行局部治疗)和10个月时出现部分缓解。第3例患有多部位内脏疾病且血清乳酸脱氢酶水平高的患者有短暂的临床获益,随后迅速出现疾病大量进展(早期进展者)。第4例患者目前正在接受BRAF/MEK抑制剂治疗,在3个月的治疗中显示出临床获益且影像学疾病稳定。不良事件可控,与首次靶向治疗期间报告的不良事件相似;4例患者中有2例在再次治疗时比首次治疗耐受性更好。