Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, and the Department of Biostatistics, Biostatistics and Bioinformatics Shared Resource Facility, University of Kentucky Chandler Medical Center-Markey Cancer Center, Lexington, Kentucky.
Obstet Gynecol. 2018 Nov;132(5):1091-1100. doi: 10.1097/AOG.0000000000002921.
To estimate the effect of ultrasound screening on stage at detection and long-term disease-specific survival of at-risk women with epithelial ovarian cancer.
Eligibility included all asymptomatic women 50 years of age or older and women 25 years of age or older with a documented family history of ovarian cancer. From 1987 to 2017, 46,101 women received annual ultrasound screening in a prospective cohort trial. Women with a persisting abnormal screen underwent tumor morphology indexing, serum biomarker analysis, and surgery.
Seventy-one invasive epithelial ovarian cancers and 17 epithelial ovarian tumors of low malignant potential were detected. No women with a low malignant potential tumor experienced recurrent disease. Stage distribution for screen-detected invasive epithelial ovarian cancers was stage I-30 (42%), stage II-15 (21%), stage III-26 (37%), and stage IV-0 (0%). Follow-up varied from 9.2 months to 27 years (mean 7.9 years). Disease-specific survival at 5, 10, and 20 years for women with invasive epithelial ovarian cancer detected by screening was 86±4%, 68±7%, and 65±7%, respectively, vs 45±2%, 31±2%, and 19±3%, respectively, for unscreened women with clinically detected ovarian cancer from the same geographic area who were treated at the same institution by the same treatment protocols (P<.001). Twenty-seven percent of screen-detected malignancies were type I and 73% were type II. The disease-specific survival of women with type I and type II screen-detected tumors was significantly higher than that of women with clinically detected type I and type II tumors and was related directly to earlier stage at detection.
Annual ultrasound screening of at-risk asymptomatic women was associated with lower stage at detection and increased 5-, 10-, and 20-year disease-specific survival of women with both type I and type II epithelial ovarian cancer.
OnCore Clinical Trials Management System, NCI-2013-01954.
评估超声筛查对高危上皮性卵巢癌女性的检出期和长期疾病特异性生存的影响。
合格的患者包括所有无症状的 50 岁及以上女性和有记录的卵巢癌家族史的 25 岁及以上女性。1987 年至 2017 年,46101 名女性参加了一项前瞻性队列试验,每年接受超声筛查。持续性异常筛查的女性进行肿瘤形态学索引、血清生物标志物分析和手术。
共发现 71 例侵袭性上皮性卵巢癌和 17 例低恶性潜能上皮性卵巢肿瘤。无一例低恶性潜能肿瘤患者出现疾病复发。筛查发现的侵袭性上皮性卵巢癌的分期分布为 I 期-30 例(42%)、II 期-15 例(21%)、III 期-26 例(37%)和 IV 期-0 例(0%)。随访时间为 9.2 个月至 27 年(平均 7.9 年)。通过筛查发现的侵袭性上皮性卵巢癌患者的 5 年、10 年和 20 年疾病特异性生存率分别为 86±4%、68±7%和 65±7%,而来自同一地理区域的相同机构按照相同治疗方案治疗的临床发现卵巢癌的未筛查女性的相应生存率分别为 45±2%、31±2%和 19±3%(P<.001)。27%的筛查性恶性肿瘤为 I 型,73%为 II 型。I 型和 II 型筛查发现肿瘤的患者疾病特异性生存率明显高于临床发现的 I 型和 II 型肿瘤患者,且与较早的检出期直接相关。
对高危无症状女性进行年度超声筛查与降低检出期和提高 I 型和 II 型上皮性卵巢癌女性的 5 年、10 年和 20 年疾病特异性生存率有关。
OnCore 临床试验管理系统,NCI-2013-01954。