医学
癌肉瘤
恶性肿瘤
癌症研究
卵巢癌
化疗
体内
免疫疗法
血管内皮生长因子
癌症
前药
肿瘤科
内科学
癌
血管内皮生长因子受体
遗传学
药理学
生物
作者
Kristy Ramphal,Matthew J. Hadfield,Christina A. Bandera,Jesse Hart,Don S. Dizon
标识
DOI:10.1097/coc.0000000000001056
摘要
Ovarian carcinosarcoma (OCS) is a rare malignancy with a poor prognosis. It is a biphasic tumor with malignant epithelial and mesenchymal components. A few mutations commonly seen in cancer have been identified in OCS, including TP53, PIK3CA, c-myc, ZNF217, ARID1A, and CTNNB1. Some OCS tumors have shown vascular endothelial growth factor positivity and limited HER2 expression. There is evidence of homologous recombination deficiency in OCS. This malignancy can be categorized as copy number high but has not been shown to have a high tumor mutational burden. There are mixed findings regarding the presence of biomarkers targeted by immune checkpoint inhibitors in OCS. For treatments other than systemic chemotherapy, the data available are largely based on in vitro and in vivo studies. In addition, there are case reports citing the use of poly-ADP ribose polymerase inhibitors, vascular endothelial growth factor inhibitors, and immunotherapy with varying degrees of success. This review paper will discuss the molecular and genomic characteristics of OCS, which can guide future treatment strategies.
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