Luzerner Kantonsspital, Lucerne, Switzerland; University of Berne, Berne, Switzerland; Swiss Group for Clinical Cancer Research (SAKK), Berne, Switzerland.
International Breast Cancer Study Group Statistical Center, Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA; Frontier Science and Technology Research Foundation, Boston, MA, USA.
Lancet Oncol. 2014 Feb;15(2):156-63. doi: 10.1016/S1470-2045(13)70589-8. Epub 2014 Jan 16.
Patients with isolated locoregional recurrences (ILRR) of breast cancer have a high risk of distant metastasis and death from breast cancer. We aimed to establish whether adjuvant chemotherapy improves the outcome of such patients.
The CALOR trial was a pragmatic, open-label, randomised trial that accrued patients with histologically proven and completely excised ILRR after unilateral breast cancer who had undergone a mastectomy or lumpectomy with clear surgical margins. Eligible patients were enrolled from hospitals worldwide and were centrally randomised (1:1) to chemotherapy (type selected by the investigator; multidrug for at least four courses recommended) or no chemotherapy, using permuted blocks, and stratified by previous chemotherapy, oestrogen-receptor and progesterone-receptor status, and location of ILRR. Patients with oestrogen-receptor-positive ILRR received adjuvant endocrine therapy, radiation therapy was mandated for patients with microscopically involved surgical margins, and anti-HER2 therapy was optional. The primary endpoint was disease-free survival. All analyses were by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00074152.
From Aug 22, 2003, to Jan 31, 2010, 85 patients were randomly assigned to receive chemotherapy and 77 were assigned to no chemotherapy. At a median follow-up of 4·9 years (IQR 3·6-6 ·0), 24 (28%) patients had disease-free survival events in the chemotherapy group compared with 34 (44%) in the no chemotherapy group. 5-year disease-free survival was 69% (95% CI 56-79) with chemotherapy versus 57% (44-67) without chemotherapy (hazard ratio 0·59 [95% CI 0·35-0·99]; p=0·046). Adjuvant chemotherapy was significantly more effective for women with oestrogen-receptor-negative ILRR (pinteraction=0·046), but analyses of disease-free survival according to the oestrogen-receptor status of the primary tumour were not statistically significant (pinteraction=0·43). Of the 81 patients who received chemotherapy, 12 (15%) had serious adverse events. The most common adverse events were neutropenia, febrile neutropenia, and intestinal infection.
Adjuvant chemotherapy should be recommended for patients with completely resected ILRR of breast cancer, especially if the recurrence is oestrogen-receptor negative.
US Department of Health and Human Services, Swiss Group for Clinical Cancer Research (SAKK), Frontier Science and Technology Research Foundation, Australian and New Zealand Breast Cancer Trials Group, Swedish Cancer Society, Oncosuisse, Cancer Association of South Africa, Foundation for Clinical Research of Eastern Switzerland (OSKK), Grupo Español de Investigación en Cáncer de Mama (GEICAM), and the Dutch Breast Cancer Trialists' Group (BOOG).
患有孤立性局部区域复发(ILRR)的乳腺癌患者有发生远处转移和死于乳腺癌的高风险。我们旨在确定辅助化疗是否能改善此类患者的预后。
CALOR 试验是一项实用的、开放标签、随机试验,招募了单侧乳腺癌完全切除后发生组织学证实的局部区域复发(ILRR)且接受了保乳手术或乳房切除术且切缘清晰的患者。来自世界各地的医院招募了符合条件的患者,并使用随机化区组(1:1)将其随机分配至接受化疗(研究者选择的类型;建议至少进行四程多药化疗)或不接受化疗,采用置换块,并按先前接受的化疗、雌激素受体和孕激素受体状态以及 ILRR 的位置进行分层。ILRR 为雌激素受体阳性的患者接受辅助内分泌治疗,对于显微镜下有受累切缘的患者需要进行放射治疗,抗 HER2 治疗为可选治疗。主要终点为无病生存。所有分析均基于意向治疗。本研究在 ClinicalTrials.gov 注册,编号为 NCT00074152。
从 2003 年 8 月 22 日至 2010 年 1 月 31 日,共有 85 名患者被随机分配接受化疗,77 名患者被分配接受无化疗。在中位随访 4.9 年(IQR 3.6-6.0)期间,化疗组中有 24 名(28%)患者发生无病生存事件,无化疗组中有 34 名(44%)患者发生。化疗组的 5 年无病生存率为 69%(95%CI 56-79),无化疗组为 57%(44-67)(风险比 0.59 [95%CI 0.35-0.99];p=0.046)。辅助化疗对雌激素受体阴性 ILRR 患者更有效(p 交互=0.046),但根据原发性肿瘤雌激素受体状态进行的无病生存分析没有统计学意义(p 交互=0.43)。在接受化疗的 81 名患者中,有 12 名(15%)发生了严重不良事件。最常见的不良事件是中性粒细胞减少症、发热性中性粒细胞减少症和肠道感染。
对于完全切除的乳腺癌 ILRR 患者,应推荐辅助化疗,特别是在复发为雌激素受体阴性时。
美国卫生与公众服务部、瑞士临床癌症研究组(SAKK)、前沿科学与技术研究基金会、澳大利亚和新西兰乳腺癌试验组、瑞典癌症协会、Oncosuisse、南非癌症协会、瑞士东部临床研究基金会(OSKK)、西班牙乳腺癌研究小组(GEICAM)和荷兰乳腺癌试验组(BOOG)。