Puglisi Fabio, Gerratana Lorenzo, Lambertini Matteo, Ceppi Marcello, Boni Luca, Montemurro Filippo, Russo Stefania, Bighin Claudia, De Laurentiis Michelino, Giuliano Mario, Bisagni Giancarlo, Durando Antonio, Turletti Anna, Garrone Ornella, Ardizzoni Andrea, Gamucci Teresa, Colantuoni Giuseppe, Gravina Adriano, De Placido Sabino, Cognetti Francesco, Del Mastro Lucia
Department of Medicine (DAME), University of Udine, Udine, Italy.
Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano (PN), Italy.
NPJ Breast Cancer. 2021 Jun 28;7(1):82. doi: 10.1038/s41523-021-00286-w.
The GIM2 phase III trial demonstrated the benefit of dose-dense chemotherapy in node-positive early breast cancer (eBC). To better define the dose-dense effect in the hormone receptor-positive subgroup, we evaluated its benefit through a composite measure of recurrence risk. We conducted an ancillary analysis of the GIM2 trial evaluating the absolute treatment effect through a composite measure of recurrence risk (CPRS) in patients with hormone receptor-positive HER2-negative eBC. CPRS was estimated through Cox proportional hazards models applied to the different clinicopathological features. The treatment effect was compared to the values of CPRS by using the Sub-population Treatment Effect Pattern Plot (STEPP) process. The Disease-Free Survival (DFS)-oriented STEPP analysis showed distinct patterns of relative treatment effect with respect to CPRS. Overall, 5-year DFS differed across CPRS quartiles ranging from 95.2 to 66.4%. Each CPRS quartile was characterized by a different patients' composition, especially for age, lymph node involvement, tumor size, estrogen and progesterone receptor expression, and Ki-67. A number needed to treat of 154 and 6 was associated with the lowest and the highest CPRS quartile, respectively. Dose-dense adjuvant chemotherapy showed a consistent benefit in node-positive eBC patients with hormone receptor-positive HER2-negative disease, but its effect varied according to CPRS.
GIM2三期试验证明了剂量密集化疗对淋巴结阳性早期乳腺癌(eBC)的益处。为了更好地确定激素受体阳性亚组中的剂量密集效应,我们通过复发风险的综合指标评估了其益处。我们对GIM2试验进行了一项辅助分析,通过激素受体阳性、HER2阴性eBC患者复发风险的综合指标(CPRS)评估绝对治疗效果。CPRS通过应用于不同临床病理特征的Cox比例风险模型进行估计。通过使用亚组治疗效果模式图(STEPP)方法将治疗效果与CPRS值进行比较。以无病生存期(DFS)为导向的STEPP分析显示了相对于CPRS的不同相对治疗效果模式。总体而言,5年DFS在CPRS四分位数之间有所不同,范围从95.2%到66.4%。每个CPRS四分位数都有不同的患者组成特征,尤其是在年龄、淋巴结受累情况、肿瘤大小、雌激素和孕激素受体表达以及Ki-67方面。治疗所需人数分别为154和6,与最低和最高CPRS四分位数相关。剂量密集辅助化疗对激素受体阳性、HER2阴性疾病的淋巴结阳性eBC患者显示出一致的益处,但其效果因CPRS而异。