Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, UK
University of Birmingham, Birmingham, UK.
Int J Gynecol Cancer. 2019 Jan;29(1):195-200. doi: 10.1136/ijgc-2018-000016.
Ovarian cancer carries a lifetime risk of approximately 2% for women and is the leading cause of death from any gynecologic malignancy. Currently, no screening program for ovarian cancer exists for the general population in the UK. This review focuses on the evidence surrounding the efficacy of current markers and discusses future improvements in screening for this disease. One-off cancer antigen 125 (CA125) measurements for detecting ovarian cancer have been well researched. However, studies have highlighted low positive predictive values (5%) and high false positive rates leading to patient anxiety and unnecessary invasive follow-up. Commonly, in the UK, CA125 is combined with transvaginal ultrasound, but there is little evidence that this approach can decrease mortality from ovarian cancer. Recently the Risk of Ovarian Cancer Algorithm, involving a combination of serial CA125 measurements and age, has been shown to detect more early stage cancers. Nevertheless, these measures are not robust in decreasing mortality from ovarian cancer and are costly to implement. Newer markers, such as human epididymis protein 4, have shown greater specificity. Its combination with CA125 and menopausal status in the Risk of Ovarian Malignancy Algorithm can predict the risk of malignancy but provides no additional benefit as a screening tool. Advanced techniques are emerging, including ultrasound molecular imaging techniques using microbubbles targeted to kinase domain receptors, and fallopian tube cytology. To reduce mortality from ovarian cancer, detection of pre-invasive lesions is imperative as ovarian cancer may develop in the fallopian tube and spread to the peritoneal cavity before being detected systemically. It seems that screening tools for ovarian cancer are currently not worthwhile for implementation into a national program. An emphasis on reducing false positives rates, associated anxiety and subsequent overdiagnosis is needed.
卵巢癌使女性终生罹患该疾病的风险约为 2%,是导致妇科恶性肿瘤死亡的主要原因。目前,英国普通人群中尚无卵巢癌筛查计划。本综述重点关注当前标志物的有效性证据,并讨论了该疾病筛查的未来改进。单次检测癌抗原 125(CA125)用于诊断卵巢癌的研究已经很多。然而,研究强调了其阳性预测值(5%)低和假阳性率高的问题,这导致了患者的焦虑和不必要的侵入性随访。在英国,CA125 通常与经阴道超声联合使用,但几乎没有证据表明这种方法可以降低卵巢癌的死亡率。最近,卵巢癌风险算法(涉及连续 CA125 测量值和年龄的组合)已被证明可以检测更多早期癌症。然而,这些方法并不能有效降低卵巢癌的死亡率,且实施成本高昂。较新型标志物,如人附睾蛋白 4,特异性更高。其与 CA125 和绝经状态在卵巢恶性肿瘤风险算法中的联合使用可以预测恶性肿瘤的风险,但作为筛查工具并无额外获益。新技术正在涌现,包括使用靶向激酶结构域受体的微泡的超声分子成像技术,以及输卵管细胞学检查。为了降低卵巢癌的死亡率,必须检测出癌前病变,因为卵巢癌可能在输卵管中发展,并在系统检测之前扩散到腹膜腔。目前,似乎卵巢癌的筛查工具并不值得在全国范围内实施。需要重点关注降低假阳性率、相关焦虑和随后的过度诊断问题。