From the Departments of Gynecologic Oncology and Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas; and Hospital de Clínicas "José de San Martín," Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina.
Obstet Gynecol. 2010 Dec;116(6):1358-1365. doi: 10.1097/AOG.0b013e3181fb8045.
To describe the clinical and pathologic features of vaginal melanoma and to determine predictors of outcome in patients with this disease.
Thirty-seven women with clinical and radiographic stage I vaginal melanoma treated at one institution between 1980 and 2009 were included in this retrospective study. Treatment modalities were assigned to one of three categories: pelvic exenteration, wide excision, and nonsurgical (primary radiation therapy, chemotherapy, or both). Overall survival and progression-free survival were calculated from the date of the surgical diagnosis.
The median age was 60.6 years. Eighty-four percent of patients were white. Vaginal bleeding was the most common presenting symptom. Lesions were located in the distal third of the vagina in the majority (65%) of patients. Initial management included a wide local or radical excision (76% of patients); pelvic exenteration (14%); and radiotherapy, chemotherapy, or radiotherapy and chemotherapy (10%). At a median follow-up of 17.4 months, 33 women experienced disease recurrence. Recurrence was local only in seven patients (22%), distant only in 20 (63%), and both in five (15%). The most common sites of distant recurrence were lungs and liver. Median progression-free survival was 11.4 months, and median overall survival was 19 months. The 5-year progression-free and overall survival rates were 9.5% and 20.0%, respectively. Patients treated surgically had significantly longer survival than those treated nonsurgically (P=.01). Radiotherapy after wide excision reduced local recurrence risk and increased survival from 16.1 months to 29.4 months, although the increase was not significant (P=.46).
Malignant vaginal melanoma, even when localized at presentation, has a very poor prognosis. Patients treated surgically have longer survival than those treated nonsurgically. Radiotherapy after wide excision reduces local but not distant recurrences.
描述阴道黑色素瘤的临床和病理特征,并确定该病患者的预后预测因素。
本回顾性研究纳入了 1980 年至 2009 年期间在一家机构接受治疗的 37 名临床和影像学 I 期阴道黑色素瘤女性患者。治疗方式分为以下三类:盆腔切除术、广泛切除术和非手术治疗(单纯放疗、化疗或联合治疗)。从手术诊断日期开始计算总生存期和无进展生存期。
中位年龄为 60.6 岁。84%的患者为白人。阴道出血是最常见的首发症状。病变位于阴道远端三分之一的患者占大多数(65%)。初始治疗包括广泛局部或根治性切除术(76%的患者)、盆腔切除术(14%)以及放疗、化疗或放化疗(10%)。中位随访时间为 17.4 个月时,33 名患者出现疾病复发。7 名患者(22%)仅出现局部复发,20 名患者(63%)仅出现远处复发,5 名患者(15%)同时出现局部和远处复发。远处复发最常见的部位是肺和肝。中位无进展生存期为 11.4 个月,中位总生存期为 19 个月。5 年无进展生存率和总生存率分别为 9.5%和 20.0%。手术治疗患者的生存时间明显长于非手术治疗患者(P=.01)。广泛切除术后放疗降低了局部复发风险,将生存时间从 16.1 个月延长至 29.4 个月,但差异无统计学意义(P=.46)。
即使在发病时局限性的阴道黑色素瘤,预后也非常差。手术治疗患者的生存时间长于非手术治疗患者。广泛切除术后放疗可降低局部复发率,但不能降低远处复发率。