Phillipps Jordan, Nassief George, Morecroft Renee, Adeyelu Tolulope, Elliott Andrew, Abdulla Farah, Vanderwalde Ari, Park Soo, Butt Omar, Zhou Alice, Ansstas George
Division of Medical Oncology, Department of Medicine, Washington University in Saint Louis, Saint Louis, MO 63130, USA.
Caris Life Sciences, Phoenix, AZ, USA.
NPJ Precis Oncol. 2024 Sep 5;8(1):187. doi: 10.1038/s41698-024-00684-w.
Modern advancements in targeted therapy and immunotherapy have significantly improved survival outcomes for advanced melanoma; however, there remains a need for novel approaches to overcome disease progression and treatment resistance. In recent years, PARPi therapy has shown great promise both as a single regimen and in combination with other therapeutics in melanoma. Here, we describe three unique cases of advanced BRAF V600 mutated melanoma that progressed on targeted BRAF/MEK agents that subsequently exhibited partial to near-complete responses to combinatory PARPi and BRAF/MEK inhibitors. This highlights both a potential synergy underlying this combinatory approach and its efficacy as a treatment option for patients with advanced melanoma refractory to targeted and/or immunotherapies. Prospective clinical trials are needed to explore this synergic effect in larger melanoma cohorts to investigate this combination for treating refractory advanced melanoma.
靶向治疗和免疫治疗的现代进展显著改善了晚期黑色素瘤的生存结果;然而,仍需要新的方法来克服疾病进展和治疗耐药性。近年来,PARPi疗法在黑色素瘤中作为单一疗法以及与其他疗法联合使用都显示出了巨大的前景。在此,我们描述了三例晚期BRAF V600突变黑色素瘤的独特病例,这些病例在靶向BRAF/MEK药物治疗下病情进展,随后对PARPi与BRAF/MEK抑制剂联合治疗表现出部分至近乎完全的反应。这突出了这种联合方法潜在的协同作用及其作为对靶向和/或免疫疗法难治的晚期黑色素瘤患者的治疗选择的疗效。需要进行前瞻性临床试验,以在更大的黑色素瘤队列中探索这种协同效应,研究这种联合疗法用于治疗难治性晚期黑色素瘤。