Ducie Jennifer A, Leitao Mario M
a Gynecology Service, Department of Surgery , Memorial Sloan Kettering Cancer Center , New York , NY , USA.
Expert Rev Anticancer Ther. 2016;16(1):45-55. doi: 10.1586/14737140.2016.1115724. Epub 2015 Nov 26.
Uterine leiomyosarcoma (uLMS) is a rare mesenchymal tumor of the gynecologic tract. Although diagnosed in only 1-3% of patients with uterine cancer, uLMS accounts for the majority of uterine cancer-related deaths. The standard of care for patients with uLMS includes total hysterectomy and bilateral salpingo-oophorectomy (BSO). There are no standard recommendations regarding adjuvant or palliative therapy. Many cytotoxic and targeted agents have been studied in clinical trials in an effort to identify an effective therapy that may alter the natural history of this disease. Unfortunately, as of now, there are no adjuvant therapy regimens that improve overall survival in this patient population. There is, therefore, an unmet need to identify a novel therapy that will improve the survival of women diagnosed with this aggressive disease. Here we summarize the existing literature on adjuvant therapy in uLMS, specifically highlighting advances made in the last 5 years.
子宫平滑肌肉瘤(uLMS)是一种罕见的妇科间叶组织肿瘤。尽管仅在1%-3%的子宫癌患者中被诊断出,但uLMS却占子宫癌相关死亡的大多数。uLMS患者的标准治疗方案包括全子宫切除术和双侧输卵管卵巢切除术(BSO)。关于辅助治疗或姑息治疗尚无标准建议。许多细胞毒性药物和靶向药物已在临床试验中进行研究,以努力确定一种可能改变该疾病自然病程的有效治疗方法。不幸的是,截至目前,尚无辅助治疗方案能改善该患者群体的总生存期。因此,迫切需要确定一种新的治疗方法,以提高被诊断患有这种侵袭性疾病的女性的生存率。在此,我们总结了关于uLMS辅助治疗的现有文献,特别强调了过去5年取得的进展。