卵巢癌筛查

P. Jani, R. Iyer
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引用次数: 0

摘要

卵巢癌通常在晚期被诊断出来,并且与较差的生存率有关。筛查的目的是发现早期疾病,以提高总体生存率。卵巢癌的发病率在低危人群中约为1-2%,在高危人群中约为10-40%。经阴道超声(TVS)和血清CA125水平已被用于早期检测。每年进行TVS和血清CA125水平筛查(使用临界值)并不能在早期发现卵巢癌。使用序列CA125水平(使用卵巢癌风险算法roca解释风险)和超声作为二线检测的多模式筛查(MMS)与每年一次的超声检测卵巢癌相比,具有更高的灵敏度。然而,没有证据表明对生存有影响,因此,不建议在一般人群或高危人群中进行筛查。现在有证据表明,高级别浆液性癌起源于输卵管,那里已经发现了前体病变。较新的筛查策略可能会将重点转移到使用新技术检测这些前体病变,如剥脱细胞学,循环肿瘤DNA和使用超声成像中的微泡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening for Ovarian Cancer
Ovarian cancer is often diagnosed at an advanced stage and is associated with poor survival. Screening aims at detection of early stage disease with a view of improving overall survival. Incidence of ovarian cancer is about 1–2% in the low-risk and 10–40% in the high-risk population. Transvaginal ultrasound (TVS) and serum CA125 levels have been used for early detection. Annual screening with TVS and serum CA125 levels (using a cutoff value) has not demonstrated detection of ovarian cancer at an early stage. Multimodal screening (MMS) using sequential CA125 levels (with interpretation of risk using Risk of Ovarian Cancer Algorithm—ROCA) and ultrasound as the second-line test have been shown to have improved sensitivity when compared to annual ultrasound in the detection of ovarian cancer. However, no impact on survival has been demonstrated, and therefore, screening cannot be recommended in the general or high-risk population. There is evidence now to suggest that high-grade serous cancers originate from the fallopian tube where precursor lesions have been identified. Newer screening strategies are likely to shift the focus to detecting these precursor lesions with novel techniques such as exfoliative cytology, circulating tumour DNA and use of microbubbles in ultrasound imaging.
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