Fornier Monica, Norton Larry
Breast Cancer Medicine Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Breast Cancer Res. 2005;7(2):64-9. doi: 10.1186/bcr1007. Epub 2005 Feb 10.
Adjuvant chemotherapy has been proven to reduce significantly the risk for relapse and death in women with operable breast cancer. Nevertheless, the prognosis for patients presenting with extensive axillary lymph node involvement remains suboptimal. In an attempt to improve on the efficacy of existing chemotherapy, a phase III intergroup trial led by the Cancer and Leukemia Group B (CALGB 97-41) was designed, which tested a mathematical model of tumor growth based on the Norton-Simon hypothesis. This hypothesis, developed about 3 decades ago, and the kinetic model derived from it, created the basis of the concepts of dose density and sequential therapy, both of which were tested in CALGB 97-41. This large prospective randomized trial demonstrated that shortening the time interval between each chemotherapy cycle while maintaining the same dose size resulted in significant improvements in disease-free and overall survival in patients with node-positive breast carcinoma. This finding is highly relevant and has immediate implications for clinical practice.
辅助化疗已被证明可显著降低可手术乳腺癌女性的复发和死亡风险。然而,出现广泛腋窝淋巴结受累的患者预后仍不理想。为了提高现有化疗的疗效,由癌症与白血病B组(CALGB 97-41)牵头开展了一项III期组间试验,该试验测试了基于诺顿-西蒙假说的肿瘤生长数学模型。这个大约30年前提出的假说及其衍生的动力学模型,构成了剂量密度和序贯治疗概念的基础,这两个概念均在CALGB 97-41中进行了测试。这项大型前瞻性随机试验表明,在保持相同剂量大小的同时缩短每个化疗周期之间的时间间隔,可显著改善淋巴结阳性乳腺癌患者的无病生存期和总生存期。这一发现具有高度相关性,对临床实践具有直接影响。