Ciaravino G., Kapp D. S., Vela A. M., Fulton R. S., Lum B. L., Teng N. N. H., Roberts J. A.
Division of Gynecologic Oncology, Department of Gynecology and Obstetrics, Stanford University School of Medicine, and Departments of Radiation Oncology and Pathology, Clinical Cancer Center, Stanford University Hospital, Stanford, California.
Int J Gynecol Cancer. 2000 Jul;10(4):340-347. doi: 10.1046/j.1525-1438.2000.010004340.x.
Primary vaginal leiomyosarcoma is a rare tumor. We report a unique case of a 27-year-old woman with stage I, high-grade primary leiomyosarcoma of the vagina treated with surgical resection and adjuvant radiation therapy. She returned within 6 months with an abdominal-pelvic recurrence and lung metastases. The patient died of disease 9 months after diagnosis. A comprehensive review of primary vaginal leiomyosarcoma was performed and factors affecting survival were analyzed. A Medline search of the English-language literature revealed 66 previously reported cases. Forty-eight of these had follow-up data. Survival probabilities were calculated using the Kaplan-Meier method, and the effects of age, stage, grade, tumor location, and treatment modality were analyzed. Stage III and IV data were combined. The overall 5-year survival rate was 43%. Patients more than 50 years of age had a 5-year survival rate of 26% compared with 51% for those less than 40 years. Five-year survival for stage I and II tumors was 55% and 44%, respectively. Patients with stage III/IV disease had 25% survival at 18 months. No patient treated primarily with chemotherapy or radiation therapy survived beyond 36 months. In contrast, patients treated primarily with surgery had a 5-year survival rate of 57%. Only stage remained an independent predictor of survival on Cox regression analysis. We continue to recommend surgical resection as primary treatment. Exenteration may be an option for select patients, but ultimately management should continue on a case-by-case basis.
原发性阴道平滑肌肉瘤是一种罕见的肿瘤。我们报告了一例独特的病例,一名27岁女性患有I期高级别原发性阴道平滑肌肉瘤,接受了手术切除及辅助放疗。她在6个月内出现腹盆腔复发及肺转移。患者在诊断后9个月死于疾病。我们对原发性阴道平滑肌肉瘤进行了全面回顾,并分析了影响生存的因素。通过对英文文献进行Medline检索,发现了66例先前报道的病例。其中48例有随访数据。使用Kaplan-Meier方法计算生存概率,并分析年龄、分期、分级、肿瘤位置和治疗方式的影响。III期和IV期数据合并分析。总体5年生存率为43%。50岁以上患者的5年生存率为26%,而40岁以下患者为51%。I期和II期肿瘤的5年生存率分别为55%和44%。III/IV期疾病患者在18个月时的生存率为25%。主要接受化疗或放疗的患者无一存活超过36个月。相比之下,主要接受手术治疗的患者5年生存率为57%。在Cox回归分析中,只有分期仍然是生存的独立预测因素。我们继续推荐手术切除作为主要治疗方法。对于部分患者,盆腔脏器清除术可能是一种选择,但最终的治疗仍应根据具体情况逐例进行。