Department of Medicine, European Institute of Oncology, Milan, Italy.
Lancet. 2013 Sep 21;382(9897):1021-8. doi: 10.1016/S0140-6736(13)61094-6. Epub 2013 Jul 18.
Trastuzumab has established efficacy against breast cancer with overexpression or amplification of the HER2 oncogene. The standard of care is 1 year of adjuvant trastuzumab, but the optimum duration of treatment is unknown. We compared 2 years of treatment with trastuzumab with 1 year of treatment, and updated the comparison of 1 year of trastuzumab versus observation at a median follow-up of 8 years, for patients enrolled in the HERceptin Adjuvant (HERA) trial.
The HERA trial is an international, multicentre, randomised, open-label, phase 3 trial comparing treatment with trastuzumab for 1 and 2 years with observation after standard neoadjuvant chemotherapy, adjuvant chemotherapy, or both in 5102 patients with HER2-positive early breast cancer. The primary endpoint was disease-free survival. The comparison of 2 years versus 1 year of trastuzumab treatment involved a landmark analysis of 3105 patients who were disease-free 12 months after randomisation to one of the trastuzumab groups, and was planned after observing at least 725 disease-free survival events. The updated intention-to-treat comparison of 1 year trastuzumab treatment versus observation alone in 3399 patients at a median follow-up of 8 years (range 0-10) is also reported. This study is registered with ClinicalTrials.gov, number NCT00045032.
We recorded 367 events of disease-free survival in 1552 patients in the 1 year group and 367 events in 1553 patients in the 2 year group (hazard ratio [HR] 0·99, 95% CI 0·85-1·14, p=0·86). Grade 3-4 adverse events and decreases in left ventricular ejection fraction during treatment were reported more frequently in the 2 year treatment group than in the 1 year group (342 [20·4%] vs 275 [16·3%] grade 3-4 adverse events, and 120 [7·2%] vs 69 [4·1%] decreases in left ventricular ejection fraction, respectively). HRs for a comparison of 1 year of trastuzumab treatment versus observation were 0·76 (95% CI 0·67-0·86, p<0·0001) for disease-free survival and 0·76 (0·65-0·88, p=0·0005) for overall survival, despite crossover of 884 (52%) patients from the observation group to trastuzumab therapy.
2 years of adjuvant trastuzumab is not more effective than is 1 year of treatment for patients with HER2-positive early breast cancer. 1 year of treatment provides a significant disease-free and overall survival benefit compared with observation and remains the standard of care.
F Hoffmann-La Roche (Roche).
曲妥珠单抗对 HER2 癌基因过度表达或扩增的乳腺癌具有明确疗效。标准治疗方法是使用曲妥珠单抗进行 1 年辅助治疗,但最佳治疗持续时间尚不清楚。我们比较了曲妥珠单抗治疗 2 年与 1 年,以及在中位随访 8 年时将 1 年曲妥珠单抗治疗与观察进行比较的更新结果,该研究入组了 HERceptin Adjuvant(HERA)试验的患者。
HERA 试验是一项国际多中心随机开放标签 3 期临床试验,比较了曲妥珠单抗治疗 1 年和 2 年与标准新辅助化疗、辅助化疗或两者联合治疗后进行观察在 5102 例 HER2 阳性早期乳腺癌患者中的疗效。主要终点是无病生存期。2 年与 1 年曲妥珠单抗治疗的比较采用了 3105 例随机分配至曲妥珠单抗组的患者的 12 个月无病生存的里程碑分析,该分析计划在观察到至少 725 例无病生存事件后进行。还报告了中位随访 8 年(范围 0-10)时 3399 例患者的 1 年曲妥珠单抗治疗与单独观察的更新意向治疗比较。该研究在 ClinicalTrials.gov 注册,编号为 NCT00045032。
我们记录了 1 年组的 1552 例患者中有 367 例无病生存事件,2 年组的 1553 例患者中有 367 例(风险比[HR]0·99,95%CI 0·85-1·14,p=0·86)。2 年治疗组与 1 年治疗组相比,3-4 级不良事件和左心室射血分数降低更为常见(342[20.4%]例与 275[16.3%]例 3-4 级不良事件,以及 120[7.2%]例与 69[4.1%]例左心室射血分数降低)。1 年曲妥珠单抗治疗与观察相比,无病生存的 HR 为 0.76(95%CI 0.67-0.86,p<0·0001),总生存的 HR 为 0.76(0.65-0.88,p=0·0005),尽管 884(52%)例观察组患者交叉至曲妥珠单抗治疗。
对于 HER2 阳性早期乳腺癌患者,曲妥珠单抗辅助治疗 2 年并不比治疗 1 年更有效。与观察相比,1 年的治疗可显著改善无病生存和总生存,仍然是标准治疗方法。
F Hoffmann-La Roche(罗氏)。