[1] Chen W,Zheng R,Baade PD,et al.Cancer statistics in China,2015[J].CA Cancer J Clin,2016,66(2):115-132.[2] Zazove P,Reed BD,Gregoire L,et al.Low false-negative rate of PCR analysis for detecting human papillomavirus-related cervical lesions[J].J Clin Microbiol,1998,36(9):2708-2713.[3] Nanda K,McCrory DC,Myers ER,et al.Accuracy of the Papanicolaou test in screening for and follow-up of cervical cytologic abnormalities:a systematic review[J].Annals Int Med,2000,132(10):810-819.[4] Katki HA,Kinney WK,Fetterman K.Cervical cancer risk for women undergoing concurrent testing for human papillomavirus and cervical cytology:a population-based study in routine clinical practice[J].Lancet Oncol,2011,12(8):722-728.[5] Castle PE,Glass AG,Rush BB,et al.Clinical human papillomavirus detection forecasts cervical cancer risk in women over 18 years of follow-up[J].J Clin Oncol,2012,30(25):3044-3050.[6] Smith RA,Manassaram-Baptiste D,Brooks D,et al.Cancer screening in the United States,2015:a review of current American cancer society guidelines and current issues in cancer screening[J].CA Cancer J Clin,2015,65(1):30-54.[7] Wentzensen N,Fetterman B,Castle PE,et al.p16/Ki-67 dual stain cytology for detection of cervical precancer in HPV-positive women[J].J Natl Cancer Inst,2015,107(12):257-261.[8] Przybycin CG, Kurman RJ, Ronnett BM,et al.Are All pelvic (nonuterine)erous carcinomas of tubal origin?[J].Am J Surg Pathol, 2010,34(10):1407-1416.[9] Kurman RJ,Shih IM.Molecular pathogenesis and extraovarian origin of epithelial ovarian cancer-shifting the paradigm[J].Hum Pathol,2011,42(7):918-931.[10] Cancer Genome Atlas Research.Integrated genomic analyses of ovarian carcinoma[J].Nature,2011,474(7353):609-615.[11] Rubin SC,Blackwood MA,Bandera C,et al.BRCA1,BRCA2,and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population:relationship to family history and implications for genetic testing[J].Am J Obstet Gynecol,1998,178(4):670-677.[12] Kauff ND,Satagopan JM,Robson ME,et al.Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation[J].New Engl J Med,2002,346(21):1609-1615.[13] Lheureux S,Shaw PA,Karakasis K,et al.Cancer precursor lesions in the BRCA population at the time of prophylactic salpingo-oophorectomy:accuracy of assessment and potential surrogate marker for prevention[J].Gynecol Oncol,2015,138(2):235-237.[14] Barton CA,Hacker NF,Clark SJ,et al.DNA methylation changes in ovarian cancer:implications for early diagnosis,prognosis and treatment[J].Gynecol Oncol,2008,109(1):129-139.[15] de Caceres II,Battagli C,Esteller M,et al.Tumor cell-specific BRCA1 and RASSF1A hypermethylation in serum,plasma,and peritoneal fluid from ovarian cancer patients[J].Cancer Res,2004,64(18):6476-6481.[16] Collins Y,Dicioccio R,Keitz B,et al.Methylation of death-associated protein kinase in ovarian carcinomas[J].Int J Gynecol Cancer,2006,16:195-199.[17] Liu B,Parsons R,Papadopoulos N,et al.Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients[J].Nature Med,1996,2(2):169-174.[18] Boland CR.A national cancer institute workshop on microsatellite instability for cancer detection and familial predisposition:development of international criteria for the determination of microsatellite instability in colorectal cancer[J].Cancer Res,1999,59(1):249-256.[19] Karlan BY,Berchuck A,Mutch D.The role of genetic testing for cancer susceptibility in gynecologic practice[J].Obstet Gynecol,2007,110(1):155-167.[20] Dove-Edwin I,Boks D,Goff S,et al.The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma[J].Cancer,2002,94(6):1708-1712.(2016-02-25收稿)