Blanc-Durand Felix, Ngoi Natalie, Lim Diana, Ray-Coquard Isabelle, Tan David Sp
Department of Haematology-Oncology, National University Cancer Institute, Singapore (NCIS), National University Hospital; Cancer Science Institute (CSI), National University of Singapore (NUS), Singapore; Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.
Department of Haematology-Oncology, National University Cancer Institute, Singapore (NCIS), National University Hospital; Cancer Science Institute (CSI), National University of Singapore (NUS), Singapore.
Cancer Treat Rev. 2025 Jul;138:102977. doi: 10.1016/j.ctrv.2025.102977. Epub 2025 Jun 13.
This review aims to consolidate the current understanding of Clear Cell Ovarian Carcinoma (CCOC), a rare yet distinct subtype of epithelial ovarian cancer. CCOC exhibits unique epidemiological, clinical and molecular features, being one of the most frequent subtypes in East Asia, often diagnosed at an early stage and frequently affecting younger women. Its hallmark characteristics include high resistance to conventional chemotherapy, poor prognosis in advanced stage and a molecular profile distinct from high-grade serous histotype. Specifically, CCOC is characterized by a low prevalence of TP53 mutations, BRCA1/2 mutations and homologous-recombination deficiency, but a high frequency of ARID1A, along with other SWI/SNF alterations, and PIK3CA mutations, both of which represent promising therapeutic targets. Despite the absence of validated therapies for CCOC so far, significant advancements in preclinical research and emerging clinical strategies including immunotherapy combinations offer hope for improved outcomes. Given the rarity of this cancer type, collaborative research and global partnerships have enabled robust studies and the implementation of trials with innovative personalized therapeutic approaches. The objective of this report is to explore the epidemiology, clinical and molecular characteristics, current standard of care and evolving therapeutic strategies for CCOC patients. It will not only highlight the progress made so far, but most importantly identifies critical research priorities to optimizing patient outcomes.
本综述旨在巩固目前对透明细胞卵巢癌(CCOC)的认识,这是一种罕见但独特的上皮性卵巢癌亚型。CCOC具有独特的流行病学、临床和分子特征,是东亚地区最常见的亚型之一,通常在早期被诊断出来,且经常影响年轻女性。其标志性特征包括对传统化疗的高抗性、晚期预后不良以及与高级别浆液性组织学类型不同的分子特征。具体而言,CCOC的特点是TP53突变、BRCA1/2突变和同源重组缺陷的发生率较低,但ARID1A以及其他SWI/SNF改变和PIK3CA突变的频率较高,这两者均代表有前景的治疗靶点。尽管目前尚无针对CCOC的有效疗法,但临床前研究的重大进展以及包括免疫疗法联合在内的新兴临床策略为改善预后带来了希望。鉴于这种癌症类型的罕见性,合作研究和全球伙伴关系使得开展有力的研究以及实施具有创新个性化治疗方法的试验成为可能。本报告的目的是探讨CCOC患者的流行病学、临床和分子特征、当前的护理标准以及不断发展的治疗策略。它不仅将突出迄今取得的进展,而且最重要的是确定优化患者预后的关键研究重点。