Miner Thomas J, Delgado Ruby, Zeisler Jonathan, Busam Klaus, Alektiar Kaled, Barakat Richard, Poynor Elizabeth
Departments of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Ann Surg Oncol. 2004 Jan;11(1):34-9. doi: 10.1007/BF02524343.
Primary vaginal melanoma is a rare and highly malignant disease. The impact of therapy on outcomes is poorly understood.
Records of all patients treated for primary vaginal melanoma at Memorial Sloan-Kettering Cancer Center from 1977 to 2001 were reviewed. Survival analysis was performed based on appropriate patient, tumor, and treatment variables. Pathologic materials were reviewed to confirm the original diagnosis and examine appropriate clinicopathologic features.
Thirty-five women were treated for vaginal melanoma; the primary treatment selected was surgical for 69% (24) and radiotherapy for 31% (11) of the patients. Surgical removal of the tumor was achieved in 92% (22) of the 24 patients selected for surgical therapy. At operation, radical excision with en bloc removal of involved pelvic organs was performed in 50% (12) of the 24 patients, a wide excision was performed in 42% (10), and a total vaginectomy was performed in 8% (2). Elective pelvic lymph node dissection was performed in 74% (26) of the 35 cases. Lymph node metastasis was found in only 8% (2) of these 26 patients. The overall median survival was 20 months. Primary surgical therapy was associated with longer overall survival (25 vs. 13 months; P =.039). Recurrence-free survival was not associated with the extent of surgery. None of the examined clinicopathologic features were associated with survival differences.
The prognosis is poor for patients with primary vaginal melanoma. Improved clinical outcomes were associated with surgical removal of gross disease whenever possible. Because of the low rate of lymph node metastasis, elective pelvic lymph node dissection is not obligatory. In cases of surgically unresectable disease, primary radiation therapy is indicated.
原发性阴道黑色素瘤是一种罕见且高度恶性的疾病。治疗对预后的影响尚不清楚。
回顾了1977年至2001年在纪念斯隆凯特琳癌症中心接受原发性阴道黑色素瘤治疗的所有患者的记录。根据适当的患者、肿瘤和治疗变量进行生存分析。对病理材料进行回顾以确认原诊断并检查适当的临床病理特征。
35名女性接受了阴道黑色素瘤治疗;所选的主要治疗方法是手术治疗,占69%(24例),放射治疗占31%(11例)。在选择手术治疗的24例患者中,92%(22例)实现了肿瘤的手术切除。手术时,24例患者中有50%(12例)进行了根治性切除并整块切除受累盆腔器官,42%(10例)进行了广泛切除,8%(2例)进行了全阴道切除术。35例中有74%(26例)进行了选择性盆腔淋巴结清扫。在这26例患者中,仅8%(2例)发现有淋巴结转移。总体中位生存期为20个月。原发性手术治疗与更长的总生存期相关(25个月对13个月;P = 0.039)。无复发生存期与手术范围无关。所检查的临床病理特征均与生存差异无关。
原发性阴道黑色素瘤患者的预后较差。只要有可能,手术切除肉眼可见的病灶与改善临床结局相关。由于淋巴结转移率低,选择性盆腔淋巴结清扫并非必需。对于手术无法切除的疾病,应进行原发性放射治疗。