摘要GS2-05:延迟开始辅助化疗对三阴性乳腺癌预后的影响

Z. Morante, R. Ruiz, G. Ku, F. Namuche, R. Mantilla, M. Luján, H. Fuentes, J. Schwarz, A. Aguilar, S. Neciosup, H. Gómez
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Patients were categorized into 4 groups according to TTC: ≤30, 31-60, 61-90, ≥91 days. We evaluated recurrence-free survival (RFS) and overall survival (OS). Logistic regression and Cox proportional hazard models were used. Results: 687 patients were included. Mean age at diagnosis was 49.15 (range, 21-89) and most patients were stage II (60.1%) or III (29.45%). They received either anthracyclines or anthracyclines and taxane-based chemotherapy (96.1%). Median TTC was 41 days. 189 (27.5%) received chemotherapy at or before 30 days; 329 (47.9%), between 31 and 60 days; 115 (16.7%), between 61 and 90 days and; 54 (7.9%) beyond 90 days. Median follow-up was 101 months. 10y-DFS was 81.4%, 68.6%, 70.8% and 68.1% among patients who received chemotherapy ≤30, 31-60, 61-90, ≥91 days, respectively (p=0.005). Accordingly, 10y-OS was 82%, 67.4%, 67.1% and 65.1% among patients who received chemotherapy ≤30, 31-60, 61-90, ≥91 days, respectively (p=0.003). In the multivariate analysis, TTC was an independent prognostic factor for RFS and OS. Patients with TTC of 31-60 days (HR, 1.92; 95% CI, 1.225 to 2.998), 61-90 days (HR, 2.38; 95% CI, 1.354 to 4.172) and ≥91days (HR, 2.47; 95% CI, 1.250 to 4.886); had worse survival compared with those who initiated treatment in the first 30 days after surgery. Patients with TTC of 31-60 days (HR, 1.94; 95% CI, 1.243 to 3.034), 61-90 days (HR, 2.45; 95% CI, 1.402 to 4.265) and ≥91days (HR, 2.79; 95% CI, 1.418 to 5.506); had worse survival compared with those who initiated treatment in the first 30 days after surgery. Conclusion: Delayed initiation of adjuvant chemotherapy in TNBC patients over 30 days is associated with a decrease in RFS and OS rates. The greater the delay, the worse the outcomes. As this represents a feasible opportunity for improvement, every attempt should be made to avoid delayed adjuvant chemotherapy initiation in this high-risk group of patients. 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引用次数: 6

摘要

背景:辅助化疗可降低复发风险,提高生存率,但尚不清楚延迟化疗是否与不良后果相关。关于三阴性乳腺癌(TNBC)的信息尤其缺乏,这是一个高危群体。我们评估了化疗时间(TTC)对TNBC患者生存结局的影响。方法:回顾性分析2000-2014年在国立肿瘤研究所接受辅助化疗的TNBC患者的病历资料。TTC定义为手术至第一次化疗之间的天数。根据TTC分为≤30天、31-60天、61-90天、≥91天4组。我们评估了无复发生存期(RFS)和总生存期(OS)。采用Logistic回归和Cox比例风险模型。结果:纳入687例患者。诊断时的平均年龄为49.15岁(范围21-89岁),大多数患者为II期(60.1%)或III期(29.45%)。接受蒽环类药物或蒽环类药物联合紫杉烷化疗(96.1%)。中位TTC为41天。189例(27.5%)在30天或之前接受化疗;329人(47.9%),在31至60天之间;115人(16.7%),61至90天;超过90天的54个(7.9%)。中位随访时间为101个月。化疗≤30天、31-60天、61-90天、≥91天患者的10y-DFS分别为81.4%、68.6%、70.8%、68.1% (p=0.005)。在化疗≤30天、31-60天、61-90天、≥91天的患者中,10y-OS分别为82%、67.4%、67.1%和65.1% (p=0.003)。在多变量分析中,TTC是RFS和OS的独立预后因素。TTC为31-60天的患者(HR, 1.92;95% CI, 1.225 ~ 2.998), 61 ~ 90天(HR, 2.38;95% CI, 1.354 ~ 4.172)和≥91天(HR, 2.47;95% CI, 1.250 ~ 4.886);与术后30天内开始治疗的患者相比,生存率更低。TTC为31-60天的患者(HR, 1.94;95% CI, 1.243 ~ 3.034), 61 ~ 90天(HR, 2.45;95% CI, 1.402 ~ 4.265)和≥91天(HR, 2.79;95% CI, 1.418 ~ 5.506);与术后30天内开始治疗的患者相比,生存率更低。结论:TNBC患者延迟开始辅助化疗超过30天与RFS和OS率降低相关。拖延得越久,结果就越糟。由于这是一个可行的改善机会,因此应尽一切努力避免这一高危患者延迟开始辅助化疗。引用格式:Morante Z, Ruiz R, De la Cruz - Ku G, Namuche F, Mantilla R, Lujan MG, Fuentes H, Schwarz J, Aguilar A, Neciosup S, Gomez H.延迟开始辅助化疗对三阴性乳腺癌预后的影响[摘要]。2018年圣安东尼奥乳腺癌研讨会论文集;2018年12月4-8日;费城(PA): AACR;癌症杂志,2019;79(4增刊):摘要nr GS2-05。
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Abstract GS2-05: Impact of the delayed initiation of adjuvant chemotherapy in the outcomes of triple negative breast cancer
Background: Adjuvant chemotherapy decreases the risk of recurrence and improves survival rates but it is unclear whether a delayed initiation is associated with adverse outcomes. Information available is especially scarce for triple negative breast cancer (TNBC) which represents a high-risk group. We evaluated the influence of time to chemotherapy (TTC) on TNBC patient9s survival outcomes. Methods: We retrospectively analyzed the data using the medical records of TNBC patients who received adjuvant chemotherapy at Instituto Nacional de Enfermedades Neoplasicas between 2000-2014. TTC was defined as the number of days between surgery and the first dose of chemotherapy. Patients were categorized into 4 groups according to TTC: ≤30, 31-60, 61-90, ≥91 days. We evaluated recurrence-free survival (RFS) and overall survival (OS). Logistic regression and Cox proportional hazard models were used. Results: 687 patients were included. Mean age at diagnosis was 49.15 (range, 21-89) and most patients were stage II (60.1%) or III (29.45%). They received either anthracyclines or anthracyclines and taxane-based chemotherapy (96.1%). Median TTC was 41 days. 189 (27.5%) received chemotherapy at or before 30 days; 329 (47.9%), between 31 and 60 days; 115 (16.7%), between 61 and 90 days and; 54 (7.9%) beyond 90 days. Median follow-up was 101 months. 10y-DFS was 81.4%, 68.6%, 70.8% and 68.1% among patients who received chemotherapy ≤30, 31-60, 61-90, ≥91 days, respectively (p=0.005). Accordingly, 10y-OS was 82%, 67.4%, 67.1% and 65.1% among patients who received chemotherapy ≤30, 31-60, 61-90, ≥91 days, respectively (p=0.003). In the multivariate analysis, TTC was an independent prognostic factor for RFS and OS. Patients with TTC of 31-60 days (HR, 1.92; 95% CI, 1.225 to 2.998), 61-90 days (HR, 2.38; 95% CI, 1.354 to 4.172) and ≥91days (HR, 2.47; 95% CI, 1.250 to 4.886); had worse survival compared with those who initiated treatment in the first 30 days after surgery. Patients with TTC of 31-60 days (HR, 1.94; 95% CI, 1.243 to 3.034), 61-90 days (HR, 2.45; 95% CI, 1.402 to 4.265) and ≥91days (HR, 2.79; 95% CI, 1.418 to 5.506); had worse survival compared with those who initiated treatment in the first 30 days after surgery. Conclusion: Delayed initiation of adjuvant chemotherapy in TNBC patients over 30 days is associated with a decrease in RFS and OS rates. The greater the delay, the worse the outcomes. As this represents a feasible opportunity for improvement, every attempt should be made to avoid delayed adjuvant chemotherapy initiation in this high-risk group of patients. Citation Format: Morante Z, Ruiz R, De la Cruz - Ku G, Namuche F, Mantilla R, Lujan MG, Fuentes H, Schwarz J, Aguilar A, Neciosup S, Gomez H. Impact of the delayed initiation of adjuvant chemotherapy in the outcomes of triple negative breast cancer [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr GS2-05.
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