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吡柔比星与表柔比星联合环磷酰胺和多西他赛用于乳腺癌新辅助化疗的对比研究

Neoadjuvant chemotherapy of breast cancer with pirarubicin versus epirubicin in combination with cyclophosphamide and docetaxel.

作者信息

Gu Xi, Jia Shi, Wei Wei, Zhang Wen-Hai

机构信息

Department of Breast Surgery, Shengjing Hospital, China Medical University, Sanhao Road No.36, Heping District, Shenyang, 110022, People's Republic of China.

出版信息

Tumour Biol. 2015 Jul;36(7):5529-35. doi: 10.1007/s13277-015-3221-9. Epub 2015 Feb 15.

Abstract

Breast cancers (BC) are treated with surgery, radiotherapy, and chemotherapy. Neoadjuvant chemotherapy (NACT) is an emerging treatment option in many cancers and is given before primary therapy to shrink tumor size. The efficacy of NACT in varied settings of BC, such as inoperable tumors, borderline resectable tumors, and breast-conserving surgery, has been debated extensively in literature, and the results remain unclear and depended on a wide variety of factors such as cancer type, disease extent, and the specific combination of chemotherapy drugs. This study was performed to examine the efficacy, toxicity, and tolerability of pirarubicin (THP) and epirubicin (EPI) in combination with docetaxel and cyclophosphamide in a NACT setting for BC. A total of 48 patients with stage II or III breast cancers were randomly divided into two groups: THP group and EPI group. The patients in THP group received 2-4 cycles of neoadjuvant chemotherapy with DTC regimen (docetaxel, THP, cyclophosphamide), while patients in the EPI group received 2-4 cycles of DEC regimen (docetaxel, EPI, cyclophosphamide) before surgery. The incidence of adverse reactions and the efficacy of the treatment regimen were compared between the two groups. Prognostic evaluation indexes were estimated by Kaplan-Meier survival analysis, including the 5-year disease-free survival (DFS) and overall survival (OS). The overall response rate in THP group was 83.3 %, and the EPI group showed a response rate of 79.2 %, with no statistically significant difference in response rate between the two groups. The incidence of cardiac toxicity, myelosuppression, nausea, and vomiting in the THP group was significantly lower than the EPI group (all P < 0.05). The incidence of hepatic toxicity, alopecia, and diarrhea in the THP group was also lower than the EPI group, but these differences were not statistically significant. The 5-year DFS and OS in THP versus EPI groups were 80 versus 76 % (DFS) and 86 versus 81 % (OS), respectively. Our study found that NACT with DTC regimen and DEC regimen were both very effective in treatment of BC. However, THP-based combination therapy was associated with significantly lower incidence of cardiac toxicity, myelosuppression, nausea, and vomiting.

摘要

乳腺癌(BC)的治疗方法包括手术、放疗和化疗。新辅助化疗(NACT)是许多癌症中一种新兴的治疗选择,在 primary therapy 之前进行以缩小肿瘤大小。NACT 在 BC 的各种情况下的疗效,如不可切除肿瘤、边界可切除肿瘤和保乳手术,在文献中已被广泛讨论,结果仍不明确,且取决于多种因素,如癌症类型、疾病范围和化疗药物的具体组合。本研究旨在探讨吡柔比星(THP)和表柔比星(EPI)联合多西他赛和环磷酰胺在 BC 的 NACT 环境中的疗效、毒性和耐受性。共有 48 例 II 期或 III 期乳腺癌患者被随机分为两组:THP 组和 EPI 组。THP 组患者接受 2 - 4 周期的 DTC 方案(多西他赛、THP、环磷酰胺)新辅助化疗,而 EPI 组患者在手术前接受 2 - 4 周期的 DEC 方案(多西他赛、EPI、环磷酰胺)。比较两组不良反应的发生率和治疗方案的疗效。通过 Kaplan - Meier 生存分析估计预后评估指标,包括 5 年无病生存率(DFS)和总生存率(OS)。THP 组的总缓解率为 83.3%,EPI 组的缓解率为 79.2%,两组缓解率无统计学显著差异。THP 组心脏毒性、骨髓抑制、恶心和呕吐的发生率显著低于 EPI 组(所有 P < 0.05)。THP 组肝毒性、脱发和腹泻的发生率也低于 EPI 组,但这些差异无统计学意义。THP 组与 EPI 组的 5 年 DFS 和 OS 分别为 80%对 76%(DFS)和 86%对 81%(OS)。我们的研究发现,DTC 方案和 DEC 方案的 NACT 在治疗 BC 方面都非常有效。然而,基于 THP 的联合治疗与心脏毒性、骨髓抑制、恶心和呕吐的发生率显著降低相关。

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