Clear cell carcinoma of the ovary (ovarian clear cell carcinoma [OvCCC]), one of subtypes of epithelial ovarian carcinoma (EOC), is often accompanied with endometriosis, which is also called as endometriosis-associated EOC (EAEOC) and frequently occurs in younger women. [1][2][3][4][5] Unsimilar to other subtypes of EOC (high-grade serous carcinoma of the ovary as an example) which are considered as a "silent killer" because symptoms of patients are often vague or asymptomatic, of short duration, often misdiagnosed as less deadly gastrointestinal diseases, and absence of an effective screening strategies, and additionally heterogeneous in nature, accounting for late diagnosis in their advanced stages, the majority of patients with OvCCC are detected in the early stage (the International Federation of Gynecology and Obstetrics stage I, especially for those patients are accompanied with endometriosis). [5][6][7][8] However, an early stage of OvCCC is not reflective of a better prognosis, since compared to other subtypes of EOC, OvCCC is always presented with its hereditary chemo-resistance status, contributing to worse prognosis. 5,9 The mechanisms of chemo-resistance status of OvCCC are extensively studied, including basic genetic changes, epigenetic modification, glycosylation, and tumor microenvironment (TME), and all of them attempt to provide a more reliable, sensitive, and specific biomarker to facilitate the purpose of screening, prompt diagnosis and/or predicting untoward outcome for patients with OvCCC, especially to distinguish OvCCC or EAEOC from pure endometriosis. 7,8,10,11 In the current issue of the Journal of the Chinese Medical Association, Dr. Chen and colleagues tried to use serum level of alpha 1-antitrypsin (AAT) isoforms (isoAAT) to examine whether this serum biomarker can be used for the aforementioned purpose. 12