乳腺癌的新辅助化疗:法国癌症中心16年来临床实践的演变和根据肿瘤亚型和临床肿瘤大小的病理反应率:回顾性队列研究。

Gilles Houvenaeghel, Alexandre de Nonneville, Monique Cohen, Frédéric Viret, Sandrine Rua, Laura Sabiani, Max Buttarelli, Emmanuelle Charaffe, Audrey Monneur, Aurélie Jalaguier-Coudray, Marie Bannier, Renaud Sabatier, Anthony Gonçalves
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引用次数: 1

摘要

我们研究了16年来接受新辅助化疗(NAC)的早期乳腺癌患者的特征趋势。我们的主要目的是分析肿瘤分期和亚型随时间的变化。次要目的包括分析手术类型和病理反应,从2005年1月到2021年5月,1623例接受NAC的患者被确定。确定了三个时期:2005-2009年(P1)、2010-2014年(P2)、2015-2021年(P3)。在单因素和多因素分析中评估周期和患者特征与cT分期、病理乳房和腋窝淋巴结反应、病理完全缓解(pCR)和手术类型之间的相关性。我们观察到cT0-1和N0分期的月经显著增加(分别从P1的6.8%增加到P3的21.2%,从P1的43.2%增加到P3的55.9%),HER2+和三阴性(TN)亚型的比例也显著增加。在多因素分析中,HER2+患者在P3期cT2-3-4肿瘤减少(OR:0.174;p=0.004)和TN肿瘤(OR:0.287;p = 0.042)。在所有患者中,分别有40.8%和34.4%的患者观察到乳腺内pCR和pCR与肿瘤亚型有很强的相关性,但在多变量分析中与肿瘤大小无关(cT0-1肿瘤中有37.0%的pCR, cT2肿瘤中有36.4%的pCR, cT3肿瘤中有29.1%的pCR (cT0-1与cT≥2;p = 0.222)。pCR与cN1分期呈负相关(OR:1.499;p
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neoadjuvant Chemotherapy for Breast Cancer: Evolution of Clinical Practice in a French Cancer Center Over 16 Years and Pathologic Response Rates According to Tumor Subtypes and Clinical Tumor Size: Retrospective Cohort Study.

Neoadjuvant Chemotherapy for Breast Cancer: Evolution of Clinical Practice in a French Cancer Center Over 16 Years and Pathologic Response Rates According to Tumor Subtypes and Clinical Tumor Size: Retrospective Cohort Study.

Neoadjuvant Chemotherapy for Breast Cancer: Evolution of Clinical Practice in a French Cancer Center Over 16 Years and Pathologic Response Rates According to Tumor Subtypes and Clinical Tumor Size: Retrospective Cohort Study.

We examined characteristics trends in early breast cancer patients receiving neoadjuvant chemotherapy (NAC) over a 16-year period. Our primary objective was to analyze variations in tumor stage and subtype over time. Secondary objectives included analyses of type of surgery and pathological response, from January 2005 to May 2021, 1623 patients receiving NAC were identified. Three periods were determined: 2005-2009 (P1), 2010-2014 (P2), 2015-2021 (P3). Correlations between periods and patient features with cT stage, pathological breast and axillary node response, pathological complete response (pCR), and type of surgery were assessed in univariate and multivariate analyses. We observed a significant increase in cT0-1 and N0 stages with periods (from 6.8% at P1 to 21.2% at P3, and from 43.2% at P1 to 55.9% at P3, respectively) and in the proportion of HER2+ and triple negative (TN) subtypes. In a multivariate analysis, a decrease of cT2-3-4 tumors during P3 was observed for HER2+ (OR:0.174; p=0.004) and TN tumors (OR:0.287; p=0.042). In-breast pCR and pCR were observed in 40.8% and 34.4% of all patients, respectively, with strong association with tumor subtypes, but not with tumor size in multivariate analysis (37.0% pCR for cT0-1 tumors, 36.4% for cT2 tumors, 29.1% for cT3 tumors (cT0-1 versus cT≥2; p=0.222)). pCR was negatively associated with cN1 stage (OR:1.499; p<0.001 for cN1 patients compared to cN0). We observed an increase in the proportion of small cT0-1 and N0 stages treated with NAC, especially in HER2+ and TN subtypes. No significant impact of tumor size on pCR rates was found.

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