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卵巢癌的筛查与检测

Screening and detection of ovarian cancer.

作者信息

Breedlove Ginger, Busenhart Cara

机构信息

University of Kansas School of Nursing, Kansas City, KS 66160, USA.

出版信息

J Midwifery Womens Health. 2005 Jan-Feb;50(1):51-4. doi: 10.1016/j.jmwh.2004.10.002.

Abstract

According to the National Cancer Institute, ovarian cancer is the sixth most common cancer in women and the leading cause of death from gynecologic malignancies. Most often the disease is advanced before symptoms are evident. It is estimated that only 15% to 30% of women in advanced stages will survive 5 years, whereas, of women in stage I at the time of diagnosis, 95% are likely to be alive in 5 years, and most are cured following surgery. Current screening techniques recommended for women with known strong risk factors include combination transvaginal sonography with cancer antigen (CA-125). Transvaginal sonography and serum CA-125 have limited diagnostic predictability. A new early detection method that uses proteomic technology will soon be available. The OvaCheck test, as researchers purport, is a highly specific and sensitive early detection method for ovarian cancer in women with strong risk factors. The Food and Drug Administration has yet to approve nationwide marketing of OvaCheck for early detection, because trials are not yet complete. Anticipated commercial availability is scheduled for early 2005.

摘要

根据美国国家癌症研究所的数据,卵巢癌是女性中第六大常见癌症,也是妇科恶性肿瘤的主要死因。大多数情况下,在症状明显之前疾病就已进展。据估计,晚期女性中只有15%至30%能存活5年,而在诊断时处于I期的女性,95%在5年后可能存活,且大多数在手术后可治愈。目前推荐给已知有高风险因素女性的筛查技术包括经阴道超声检查联合癌抗原(CA - 125)检测。经阴道超声检查和血清CA - 125的诊断预测性有限。一种使用蛋白质组学技术的新的早期检测方法即将问世。研究人员称,OvaCheck检测是一种针对有高风险因素女性的卵巢癌高度特异性和敏感性的早期检测方法。美国食品药品监督管理局尚未批准OvaCheck在全国范围内用于早期检测的市场推广,因为试验尚未完成。预计商业上市时间定在2005年初。

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