Ostby Stuart A, Daniel Saige, Kalogera Eleftheria, De Vitis Luigi, Fought Angela J, McGree Michaela E, Langstraat Carrie L, Block Matthew S
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Mayo Clinic, Rochester, MN, USA.
Department of Internal Medicine, University of California San Francisco, San Francisco, CA, USA.
Gynecol Oncol Rep. 2024 Aug 13;55:101483. doi: 10.1016/j.gore.2024.101483. eCollection 2024 Oct.
Vulvar melanoma and vaginal melanoma are rare and difficult to treat. We describe the last three decades in a cohort predominantly treated surgically with adjuvant therapy.
All new patients between 1993 and 2021 followed until 2024. Collection of demographic and oncologic data allowed comparisons and Kaplan-Meier method was used to evaluate overall survival (OS) and progression free survival (PFS) stratified by adjuvant therapy type, diagnosis before and after 2011, and between vulvar and vaginal melanomas.
Consultation for 63/72 patients (87.5 %) were for primary treatment. Most patients had vulvar melanoma (50/72, 69.4 %), received surgery (65/72, 90.3 %), and adjuvant treatment (40/72, 55.6 %) with immunotherapy, chemotherapy, and/or targeted therapy. Median survival for 63 patients presenting for primary treatment was 54.2 months, and 9/13 patients who were disease free after five years later received adjuvant immunotherapy. Survival did not vary by adjuvant therapy type or diagnosis after 2011 but was significantly less for vaginal melanoma. Following recurrence seven patients experienced complete response including three patients receiving combined nivolumab with ipilimumab and two nivolumab alone experienced.
Survival was not significantly different by adjuvant therapy type or after 2011. Most patients who were disease-free five years after surgery had received adjuvant therapy. Seven patients experienced complete responses to therapy after recurrence of whom five received immune checkpoint inhibitors. Although survival is not improved as in cutaneous melanomas by immune checkpoint inhibitors, signal continues for the use of immune checkpoint inhibitors in gynecologic melanomas.
外阴黑色素瘤和阴道黑色素瘤较为罕见且难以治疗。我们描述了过去三十年中一组主要接受手术及辅助治疗的患者情况。
纳入1993年至2021年期间所有新患者并随访至2024年。收集人口统计学和肿瘤学数据进行比较,采用Kaplan-Meier方法评估总生存期(OS)和无进展生存期(PFS),并按辅助治疗类型、2011年前后的诊断以及外阴和阴道黑色素瘤进行分层。
63/72例患者(87.5%)因初次治疗前来咨询。大多数患者患有外阴黑色素瘤(50/72,69.4%),接受了手术(65/72,90.3%)以及免疫治疗、化疗和/或靶向治疗的辅助治疗(40/72,55.6%)。63例接受初次治疗患者的中位生存期为54.2个月,13例五年后无疾病患者中有9例接受了辅助免疫治疗。生存期不因辅助治疗类型或2011年后的诊断而有所不同,但阴道黑色素瘤患者的生存期明显较短。复发后,7例患者出现完全缓解,其中3例接受纳武单抗联合伊匹木单抗治疗,2例仅接受纳武单抗治疗。
辅助治疗类型或2011年后的生存期无显著差异。大多数术后五年无疾病的患者接受了辅助治疗。7例患者复发后对治疗产生完全缓解,其中5例接受免疫检查点抑制剂治疗。尽管免疫检查点抑制剂并未如皮肤黑色素瘤那样提高生存率,但在妇科黑色素瘤中使用免疫检查点抑制剂仍有一定迹象。