Department of Surgical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Dr Ernest Borges Road, Parel, Mumbai 400 012, Maharashtra, India
Centre for Cancer Epidemiology, Department of Preventive Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Parel, Mumbai, India.
BMJ. 2021 Feb 24;372:n256. doi: 10.1136/bmj.n256.
To test the efficacy of screening by clinical breast examination in downstaging breast cancer at diagnosis and in reducing mortality from the disease, when compared with no screening.
Prospective, cluster randomised controlled trial.
20 geographically distinct clusters located in Mumbai, India, randomly allocated to 10 screening and 10 control clusters; total trial duration was 20 years (recruitment began in May 1998; database locked in March 2019 for analysis).
151 538 women aged 35-64 with no history of breast cancer.
Women in the screening arm (n=75 360) received four screening rounds of clinical breast examination (conducted by trained female primary health workers) and cancer awareness every two years, followed by five rounds of active surveillance every two years. Women in the control arm (n=76 178) received one round of cancer awareness followed by eight rounds of active surveillance every two years.
Downstaging of breast cancer at diagnosis and reduction in mortality from breast cancer.
Breast cancer was detected at an earlier age in the screening group than in the control group (age 55.18 (standard deviation 9.10) 56.50 (9.10); P=0.01), with a significant reduction in the proportion of women with stage III or IV disease (37% (n=220) 47% (n=271), P=0.001). A non-significant 15% reduction in breast cancer mortality was observed in the screening arm versus control arm in the overall study population (age 35-64; 20.82 deaths per 100 000 person years (95% confidence interval 18.25 to 23.97) 24.62 (21.71 to 28.04); rate ratio 0.85 (95% confidence interval 0.71 to 1.01); P=0.07). However, a post hoc subset analysis showed nearly 30% relative reduction in breast cancer mortality in women aged 50 and older (24.62 (20.62 to 29.76) 34.68 (27.54 to 44.37); 0.71 (0.54 to 0.94); P=0.02), but no significant reduction in women younger than 50 (19.53 (17.24 to 22.29) 21.03 (18.97 to 23.44); 0.93 (0.79 to 1.09); P=0.37). A 5% reduction in all cause mortality was seen in the screening arm versus the control arm, but it was not statistically significant (rate ratio 0.95 (95% confidence interval 0.81 to 1.10); P=0.49).
These results indicate that clinical breast examination conducted every two years by primary health workers significantly downstaged breast cancer at diagnosis and led to a non-significant 15% reduction in breast cancer mortality overall (but a significant reduction of nearly 30%in mortality in women aged ≥50). No significant reduction in mortality was seen in women younger than 50 years. Clinical breast examination should be considered for breast cancer screening in low and middle income countries.
Clinical Trials Registry of India CTRI/2010/091/001205; ClinicalTrials.gov NCT00632047.
通过临床乳房检查来检测乳腺癌降期,并降低乳腺癌死亡率,与不进行筛查相比。
前瞻性、整群随机对照试验。
印度孟买的 20 个地理位置不同的集群,随机分配到 10 个筛查组和 10 个对照组;总试验持续时间为 20 年(招募于 1998 年 5 月开始;数据库于 2019 年 3 月锁定进行分析)。
151538 名年龄在 35-64 岁之间、无乳腺癌病史的女性。
筛查组(n=75360)接受了 4 轮临床乳房检查(由经过培训的女性初级卫生工作者进行)和每两年一次的癌症意识教育,随后每两年进行 5 轮主动监测。对照组(n=76178)接受了一轮癌症意识教育,随后每两年进行 8 轮主动监测。
乳腺癌降期诊断和降低乳腺癌死亡率。
与对照组相比,筛查组的乳腺癌发病年龄更早(年龄 55.18(标准差 9.10) 56.50(9.10);P=0.01),III 期或 IV 期疾病的比例显著降低(37%(n=220) 47%(n=271);P=0.001)。在整个研究人群中(年龄 35-64 岁),筛查组与对照组相比,乳腺癌死亡率降低了 15%,但无统计学意义(20.82 例/100000 人年(95%置信区间 18.25 至 23.97) 24.62(21.71 至 28.04);率比 0.85(95%置信区间 0.71 至 1.01);P=0.07)。然而,事后亚组分析显示,年龄在 50 岁及以上的女性乳腺癌死亡率降低了近 30%(24.62(20.62 至 29.76) 34.68(27.54 至 44.37);0.71(0.54 至 0.94);P=0.02),但年龄在 50 岁以下的女性无显著降低(19.53(17.24 至 22.29) 21.03(18.97 至 23.44);0.93(0.79 至 1.09);P=0.37)。与对照组相比,筛查组的全因死亡率降低了 5%,但无统计学意义(率比 0.95(95%置信区间 0.81 至 1.10);P=0.49)。
这些结果表明,由初级卫生工作者每两年进行一次的临床乳房检查显著降低了乳腺癌的诊断分期,并导致乳腺癌死亡率总体降低了 15%(但在 50 岁及以上的女性中,死亡率显著降低了近 30%)。在年龄小于 50 岁的女性中,死亡率没有显著降低。在中低收入国家,临床乳房检查可用于乳腺癌筛查。
印度临床试验注册中心 CTRI/2010/091/001205;ClinicalTrials.gov NCT00632047。