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Safety and Efficacy of Pegylated Liposomal Doxorubicin-based Adjuvant Chemotherapy in Patients with Stage I-III Triple-negative Breast Cancer

机译:聚乙二醇化脂质体阿霉素辅助化疗对I-III期三阴性乳腺癌患者的安全性和有效性

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Background/Aim: Pegylated liposomal doxorubicin (PLD) has been proven to be an effective antitumor drug for metastatic breast cancer, with less toxicity than conventional anthracycline. Our objective was to evaluate the efficacy and safety of PLD-based adjuvant chemotherapy compared to conventional chemotherapy for patients with stages I-III Triple-negative breast cancer (TNBC). Patients and Methods: A total of 162 patients, histologically proven to have TNBC at stages I-III between 2003 and 2010, were enrolled to evaluate the impact of PLD- and non-PLD-based adjuvant chemotherapy by using the end-pint of overall survival (OS) and relapse-free survival (RFS). Results: Forty-nine (30.2%) patients received PLD-based adjuvant chemotherapy and 113 (69.8%) a non-PLD regimen, including 84 (52%) patients receiving non-PLD anthracycline. The Kaplan-Meier calculation indicated no differences in RFS and OS between the PLD and non-PLD groups. Multivariate analysis adjusted for tumor size and lymph node status also revealed similar RFS (HR=0.86, 95% CI=0.43-1.73, p=0.678) and OS (HR=0.86, 95% CI=0.41-1.79, p=0.692) for PLD-based chemotherapy compared with non-PLD-based. Patients receiving PLD-based chemotherapy had a relatively lower incidence of grade 3-4 neutropenia (25% vs. 41.6%, respectively; p=0.054) and significantly higher incidence of hand foot syndrome (16.3% vs. 4.4%, respectively; p=0.010). Conclusion: PLD-based adjuvant chemotherapy was as effective as conventional chemotherapy for patients with TNBC. PLD is an alternative for patients with TNBC when conventional anthracycline is inappropriate.
机译:背景/目的:聚乙二醇脂质体阿霉素(PLD)已被证明是一种有效的抗转移性乳腺癌抗肿瘤药物,其毒性比常规蒽环类药物低。我们的目的是评估I-III期三阴性乳腺癌(TNBC)患者与常规化疗相比基于PLD的辅助化疗的疗效和安全性。患者和方法:纳入了162例经组织学证实在2003年至2010年之间处于I-III期的TNBC的患者,以评估总PLD和非PLD辅助化疗的影响生存期(OS)和无复发生存期(RFS)。结果:四十九(30.2%)的患者接受了基于PLD的辅助化疗,其中113(69.8%)的患者采用了非PLD方案,其中84(52%)的患者接受了非PLD蒽环类药物。 Kaplan-Meier计算表明,PLD和非PLD组之间的RFS和OS没有差异。调整肿瘤大小和淋巴结状态的多变量分析也显示相似的RFS(HR = 0.86,95%CI = 0.43-1.73,p = 0.678)和OS(HR = 0.86,95%CI = 0.41-1.79,p = 0.692)基于PLD的化疗与非基于PLD的化疗相比。接受基于PLD的化学疗法的患者发生3-4级中性粒细胞减少症的发生率相对较低(分别为25%和41.6%; p = 0.054)和明显较高的手足综合征发生率(分别为16.3%和4.4%; p = 0.010)。结论:基于PLD的辅助化疗对TNBC患者的疗效与常规化疗相同。当传统的蒽环类抗生素不合适时,PLD可替代TNBC。

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