Skin and Renal Units, The Royal Marsden Hospital NHS Foundation Trust, London, UK; Melanoma and Kidney Cancer Team, The Institute of Cancer Research, London, UK.
Cancer Research UK Manchester Institute, The University of Manchester, Manchester, UK.
Cell Rep Med. 2024 Mar 19;5(3):101435. doi: 10.1016/j.xcrm.2024.101435. Epub 2024 Feb 27.
Mucosal (MM) and acral melanomas (AM) are rare melanoma subtypes of unmet clinical need; 15%-20% harbor KIT mutations potentially targeted by small-molecule inhibitors, but none yet approved in melanoma. This multicenter, single-arm Phase II trial (NICAM) investigates nilotinib safety and activity in KIT mutated metastatic MM and AM. KIT mutations are identified in 39/219 screened patients (18%); of 29/39 treated, 26 are evaluable for primary analysis. Six patients were alive and progression free at 6 months (local radiology review, 25%); 5/26 (19%) had objective response at 12 weeks; median OS was 7.7 months; ddPCR assay correctly identifies KIT alterations in circulating tumor DNA (ctDNA) in 16/17 patients. Nilotinib is active in KIT-mutant AM and MM, comparable to other KIT inhibitors, with demonstrable activity in nonhotspot KIT mutations, supporting broadening of KIT evaluation in AM and MM. Our results endorse further investigations of nilotinib for the treatment of KIT-mutated melanoma. This clinical trial was registered with ISRCTN (ISRCTN39058880) and EudraCT (2009-012945-49).
黏膜(MM)和肢端黑色素瘤(AM)是未满足临床需求的罕见黑色素瘤亚型;15%-20%的患者存在潜在的小分子抑制剂靶点 KIT 突变,但在黑色素瘤中尚未有药物获批。本多中心、单臂 II 期试验(NICAM)研究了尼洛替尼在 KIT 突变转移性 MM 和 AM 中的安全性和活性。在 39/219 例筛选患者中确定了 KIT 突变(18%);在 29/39 例治疗患者中,26 例可用于主要分析。6 例患者在 6 个月时存活且无疾病进展(局部放射学审查,25%);12 周时 5/26 例(19%)有客观缓解;中位 OS 为 7.7 个月;ddPCR 检测法可在 17/17 例患者的循环肿瘤 DNA(ctDNA)中正确识别 KIT 改变。尼洛替尼在 KIT 突变的 AM 和 MM 中具有活性,与其他 KIT 抑制剂相当,对非热点 KIT 突变具有明显的活性,支持在 AM 和 MM 中扩大 KIT 评估。我们的结果支持进一步研究尼洛替尼治疗 KIT 突变型黑色素瘤。这项临床试验已在 ISRCTN(ISRCTN39058880)和 EudraCT(2009-012945-49)注册。