Noiver Graciano, Lucelly López, Carlos A Rodriguez, Katherine Montoya, Diego M González, Luis Rodolfo Gómez, Maycos L Zapata, Javier Cortés
{"title":"化疗时间对三阴性乳腺癌的影响:一项真实世界的证据研究。","authors":"Noiver Graciano, Lucelly López, Carlos A Rodriguez, Katherine Montoya, Diego M González, Luis Rodolfo Gómez, Maycos L Zapata, Javier Cortés","doi":"10.1007/s10549-025-07716-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Triple-negative breast cancer (TNBC) is an aggressive, heterogeneous malignancy with poor prognosis. The optimal timing of chemotherapy-neoadjuvant (NACT) versus adjuvant (ACT)-remains controversial. This study assessed real-world outcomes in non-metastatic TNBC patients according to chemotherapy timing.</p><p><strong>Methods: </strong>This retrospective study (2008-2023) evaluated the impact of chemotherapy timing on overall survival (OS) and event-free survival (EFS) in a cohort of 711 patients. Propensity score (PS) matching with preoperative variables was used to adjust for baseline imbalances, and Cox regression models were applied to account for treatment-related variables.</p><p><strong>Results: </strong>NACT was administered to 525 patients (73.8%), with a 37.3% pathological complete response (pCR) rate. PS matching yielded 177 patient pairs; tumor stage, age and histologic grade remained unbalanced. In the unadjusted analysis, NACT was associated with worse OS (HR 1.56, 95% CI1.08-2.25, p = 0.018). However, multivariate analysis adjusting for unmatched and postoperative variables showed a potential benefit of NACT for OS (HR 0.53, 95% CI 0.07-4.13, p = 0.545) and EFS (HR 0.94, 95% CI 0.21-4.17, p = 0.932). Tumor stage acted as an effect modifier, and stratified analyses revealed that NACT was superior to ACT in patients with advanced-stage disease who achieved pCR (HR 0.22, 95% CI 0.07-0.7, p < 0.010).</p><p><strong>Conclusions: </strong>In our TNBC cohort, chemotherapy timing significantly influenced OS and EFS, particularly in relation to initial tumor stage and pCR status. NACT was more beneficial than ACT in patients with advanced disease who achieve pCR, underscoring its role in both prognostic stratification and therapeutic decision-making.</p>","PeriodicalId":9133,"journal":{"name":"Breast Cancer Research and Treatment","volume":" ","pages":"225-236"},"PeriodicalIF":3.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of chemotherapy timing in triple-negative breast cancer: a real-world evidence study.\",\"authors\":\"Noiver Graciano, Lucelly López, Carlos A Rodriguez, Katherine Montoya, Diego M González, Luis Rodolfo Gómez, Maycos L Zapata, Javier Cortés\",\"doi\":\"10.1007/s10549-025-07716-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Triple-negative breast cancer (TNBC) is an aggressive, heterogeneous malignancy with poor prognosis. The optimal timing of chemotherapy-neoadjuvant (NACT) versus adjuvant (ACT)-remains controversial. This study assessed real-world outcomes in non-metastatic TNBC patients according to chemotherapy timing.</p><p><strong>Methods: </strong>This retrospective study (2008-2023) evaluated the impact of chemotherapy timing on overall survival (OS) and event-free survival (EFS) in a cohort of 711 patients. Propensity score (PS) matching with preoperative variables was used to adjust for baseline imbalances, and Cox regression models were applied to account for treatment-related variables.</p><p><strong>Results: </strong>NACT was administered to 525 patients (73.8%), with a 37.3% pathological complete response (pCR) rate. PS matching yielded 177 patient pairs; tumor stage, age and histologic grade remained unbalanced. In the unadjusted analysis, NACT was associated with worse OS (HR 1.56, 95% CI1.08-2.25, p = 0.018). However, multivariate analysis adjusting for unmatched and postoperative variables showed a potential benefit of NACT for OS (HR 0.53, 95% CI 0.07-4.13, p = 0.545) and EFS (HR 0.94, 95% CI 0.21-4.17, p = 0.932). Tumor stage acted as an effect modifier, and stratified analyses revealed that NACT was superior to ACT in patients with advanced-stage disease who achieved pCR (HR 0.22, 95% CI 0.07-0.7, p < 0.010).</p><p><strong>Conclusions: </strong>In our TNBC cohort, chemotherapy timing significantly influenced OS and EFS, particularly in relation to initial tumor stage and pCR status. 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引用次数: 0
摘要
目的:三阴性乳腺癌(TNBC)是一种侵袭性、异质性、预后差的恶性肿瘤。化疗的最佳时机-新辅助(NACT)还是辅助(ACT)-仍然存在争议。该研究根据化疗时间评估了非转移性TNBC患者的实际预后。方法:本回顾性研究(2008-2023)评估了化疗时间对711例患者总生存期(OS)和无事件生存期(EFS)的影响。倾向评分(PS)与术前变量匹配用于调整基线失衡,Cox回归模型用于解释治疗相关变量。结果:525例患者(73.8%)接受NACT治疗,病理完全缓解率(pCR)为37.3%。PS配对得到177对患者;肿瘤分期、年龄和组织学分级仍不平衡。在未经调整的分析中,NACT与较差的OS相关(HR 1.56, 95% CI1.08-2.25, p = 0.018)。然而,调整未匹配变量和术后变量的多变量分析显示,NACT对OS (HR 0.53, 95% CI 0.07-4.13, p = 0.545)和EFS (HR 0.94, 95% CI 0.21-4.17, p = 0.932)有潜在的益处。肿瘤分期是一个效应修饰因子,分层分析显示,在获得pCR的晚期疾病患者中,NACT优于ACT (HR 0.22, 95% CI 0.07-0.7, p)。结论:在我们的TNBC队列中,化疗时间显著影响OS和EFS,特别是与初始肿瘤分期和pCR状态有关。在达到pCR的晚期疾病患者中,NACT比ACT更有益,强调了其在预后分层和治疗决策中的作用。
Effect of chemotherapy timing in triple-negative breast cancer: a real-world evidence study.
Purpose: Triple-negative breast cancer (TNBC) is an aggressive, heterogeneous malignancy with poor prognosis. The optimal timing of chemotherapy-neoadjuvant (NACT) versus adjuvant (ACT)-remains controversial. This study assessed real-world outcomes in non-metastatic TNBC patients according to chemotherapy timing.
Methods: This retrospective study (2008-2023) evaluated the impact of chemotherapy timing on overall survival (OS) and event-free survival (EFS) in a cohort of 711 patients. Propensity score (PS) matching with preoperative variables was used to adjust for baseline imbalances, and Cox regression models were applied to account for treatment-related variables.
Results: NACT was administered to 525 patients (73.8%), with a 37.3% pathological complete response (pCR) rate. PS matching yielded 177 patient pairs; tumor stage, age and histologic grade remained unbalanced. In the unadjusted analysis, NACT was associated with worse OS (HR 1.56, 95% CI1.08-2.25, p = 0.018). However, multivariate analysis adjusting for unmatched and postoperative variables showed a potential benefit of NACT for OS (HR 0.53, 95% CI 0.07-4.13, p = 0.545) and EFS (HR 0.94, 95% CI 0.21-4.17, p = 0.932). Tumor stage acted as an effect modifier, and stratified analyses revealed that NACT was superior to ACT in patients with advanced-stage disease who achieved pCR (HR 0.22, 95% CI 0.07-0.7, p < 0.010).
Conclusions: In our TNBC cohort, chemotherapy timing significantly influenced OS and EFS, particularly in relation to initial tumor stage and pCR status. NACT was more beneficial than ACT in patients with advanced disease who achieve pCR, underscoring its role in both prognostic stratification and therapeutic decision-making.
期刊介绍:
Breast Cancer Research and Treatment provides the surgeon, radiotherapist, medical oncologist, endocrinologist, epidemiologist, immunologist or cell biologist investigating problems in breast cancer a single forum for communication. The journal creates a "market place" for breast cancer topics which cuts across all the usual lines of disciplines, providing a site for presenting pertinent investigations, and for discussing critical questions relevant to the entire field. It seeks to develop a new focus and new perspectives for all those concerned with breast cancer.