Pinsky Paul F, Yu Kelly, Kramer Barnett S, Black Amanda, Buys Saundra S, Partridge Edward, Gohagan John, Berg Christine D, Prorok Philip C
Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, United States.
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, United States.
Gynecol Oncol. 2016 Nov;143(2):270-275. doi: 10.1016/j.ygyno.2016.08.334. Epub 2016 Sep 9.
The Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial originally reported no mortality benefit of ovarian cancer screening after a median of 12.4years of follow-up. The UKCTOCS screening trial failed to show a statistically significant mortality reduction in the primary analysis but reported an apparent increased mortality benefit in trial years 7-14 compared to 0-7. Here we report an updated analysis of PLCO with extended mortality follow-up.
Participants were randomized from 1993 to 2001 at ten U.S. centers to an intervention or usual care arm. Intervention arm women were screened for ovarian cancer with annual trans-vaginal ultrasound (TVU) (4years) and CA-125 (6years), with a fixed cutoff at 35U/mL for CA-125. The original follow-up period was for up to 13years (median follow-up 12.4years); in this analysis follow-up for mortality was extended by up to 6years.
39,105 (intervention) and 39,111 (usual care) women were randomized, of which 34,253 and 34,304, respectively, had at least one ovary at baseline. Median follow-up was 14.7years in each arm and maximum follow-up 19.2years in each arm. A total of 187 (intervention) and 176 (usual care) deaths from ovarian cancer were observed, for a risk-ratio of 1.06 (95% CI: 0.87-1.30). Risk-ratios were similar for study years 0-7 (RR=1.04), 7-14 (RR=1.06) and 14+ (RR=1.09). The risk ratio for all-cause mortality was 1.01 (95% CI: 0.97-1.05). Ovarian cancer specific survival was not significantly different across trial arms (p=0.16).
Extended follow-up of PLCO indicated no mortality benefit from screening for ovarian cancer with CA-125 and TVU.
前列腺、肺、结直肠癌和卵巢癌(PLCO)筛查试验最初报告称,在中位随访12.4年后,卵巢癌筛查未显示出对死亡率的益处。英国癌症筛查协作组(UKCTOCS)筛查试验在初步分析中未显示出统计学上显著的死亡率降低,但报告称与0至7年相比,在试验的第7至14年有明显增加的死亡率益处。在此,我们报告了对PLCO进行延长死亡率随访后的更新分析。
1993年至2001年期间,美国十个中心的参与者被随机分配到干预组或常规护理组。干预组的女性每年接受经阴道超声检查(TVU)(共4年)和CA-125检测(共6年)进行卵巢癌筛查,CA-125的固定临界值为35U/mL。最初的随访期长达13年(中位随访12.4年);在本次分析中,死亡率随访延长至6年。
39,105名(干预组)和39,111名(常规护理组)女性被随机分组,其中分别有34,253名和34,304名在基线时至少有一个卵巢。每组的中位随访时间为14.7年,每组的最长随访时间为19.2年。共观察到187例(干预组)和176例(常规护理组)卵巢癌死亡病例,风险比为1.06(95%置信区间:0.