Kanthan Rani, Senger Jenna-Lynn
Department of Pathology and Laboratory Medicine, University of Saskatchewan, Saskatoon, SK, Canada S7N 0W8.
Obstet Gynecol Int. 2011;2011:470795. doi: 10.1155/2011/470795. Epub 2011 Oct 5.
Uterine carcinosarcomas (MMMT-malignant mixed Müllerian tumours) are highly aggressive, rare, biphasic tumours composed of epithelial and mesenchymal elements believed to arise from a monoclonal origin. While hysterectomy with bilateral salpingo-oophorectomy remains the mainstay treatment, high rates of recurrence and metastases suggest a need for lymphadenectomy and postoperative adjuvant treatment. There are no established consensus guidelines for therapeutic patient management. Though well recognized that it improves locoregional control, the role of radiation in improving overall survival outcomes remains undecided. Although various combinations of chemotherapy have been explored, an optimal therapeutic modality is yet to be determined. As overall survival rates have not improved in thirty years, it is suggested that targeted chemotherapy and/or a multimodality approach may yield better outcomes. This paper provides a summary of the aetiopathogenesis of carcinosarcomas (MMMT) limited to the uterus with special emphasis on the controversies in the management of these patients.
子宫癌肉瘤(恶性混合性苗勒管肿瘤)是一种侵袭性很强、罕见的双相肿瘤,由上皮和间充质成分组成,被认为起源于单克隆。虽然子宫切除术加双侧输卵管卵巢切除术仍然是主要治疗方法,但高复发率和转移率表明需要进行淋巴结清扫术和术后辅助治疗。目前尚无针对治疗患者管理的既定共识指南。尽管人们普遍认识到放疗可改善局部控制,但放疗在改善总体生存结果方面的作用仍未确定。虽然已经探索了各种化疗组合,但尚未确定最佳治疗方式。由于三十年来总体生存率没有提高,有人建议靶向化疗和/或多模式方法可能会产生更好的结果。本文总结了局限于子宫的癌肉瘤(恶性混合性苗勒管肿瘤)的病因发病机制,特别强调了这些患者管理中的争议。