Jacobs I J, Skates S J, MacDonald N, Menon U, Rosenthal A N, Davies A P, Woolas R, Jeyarajah A R, Sibley K, Lowe D G, Oram D H
Department of Gynaecological Oncology, St Bartholomew's and Royal London School of Medicine and Dentistry, Queen Mary and Westfield College, UK.
Lancet. 1999 Apr 10;353(9160):1207-10. doi: 10.1016/S0140-6736(98)10261-1.
The value of screening for ovarian cancer is uncertain. We did a pilot randomised trial to assess multimodal screening with sequential CA 125 antigen and ultrasonography.
Postmenopausal women aged 45 years or older were randomised to a control group (n=10,977) or screened group (n=10,958). Women randomised to screening were offered three annual screens that involved measurement of serum CA 125, pelvic ultrasonography if CA 125 was 30 U/mL or more, and referral for gynaecological opinion if ovarian volume was 8.8 mL or more on ultrasonography. All women were followed up to see whether they developed invasive epithelial cancers of the ovary or fallopian tube (index cancers).
Of 468 women in the screened group with a raised CA 125, 29 were referred for a gynaecological opinion; screening detected an index cancer in six and 23 had false-positive screening results. The positive predictive value was 20.7%. During 7-year follow-up, ten further women with index cancers were identified in the screened group and 20 in the control group. Median survival of women with index cancers in the screened group was 72.9 months and in the control group was 41.8 months (p=0.0112). The number of deaths from an index cancer did not differ significantly between the control and screened groups (18 of 10,977 vs nine of 10,958, relative risk 2.0 [95% CI 0.78-5.13]).
These results show that a multimodal approach to ovarian cancer screening in a randomised trial is feasible and justify a larger randomised trial to see whether screening affects mortality.
卵巢癌筛查的价值尚不确定。我们开展了一项试点随机试验,以评估采用CA 125抗原和超声检查的多模式筛查。
将45岁及以上的绝经后女性随机分为对照组(n = 10977)或筛查组(n = 10958)。被随机分配到筛查组的女性接受为期三年的筛查,包括检测血清CA 125,若CA 125≥30 U/mL则进行盆腔超声检查,若超声检查显示卵巢体积≥8.8 mL则转诊至妇科进行评估。对所有女性进行随访,观察她们是否发生卵巢或输卵管浸润性上皮癌(索引癌)。
在筛查组中,468名CA 125升高的女性中有29名被转诊至妇科进行评估;筛查发现6例索引癌,23例筛查结果为假阳性。阳性预测值为20.7%。在7年的随访期间,筛查组又发现10例索引癌患者,对照组发现20例。筛查组中索引癌患者的中位生存期为72.9个月,对照组为41.8个月(p = 0.0112)。对照组和筛查组因索引癌死亡的人数无显著差异(10977例中有18例,10958例中有9例,相对风险2.0 [95% CI 0.78 - 5.13])。
这些结果表明,在随机试验中采用多模式方法进行卵巢癌筛查是可行的,有必要开展更大规模的随机试验以确定筛查是否会影响死亡率。