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一项大型或局部晚期可手术乳腺癌患者接受吉西他滨和多柔比星序贯新辅助化疗后再接受吉西他滨和顺铂治疗的 2 期研究:长期随访结果。

A phase 2 study of sequential neoadjuvant chemotherapy with gemcitabine and doxorubicin followed by gemcitabine and cisplatin in patients with large or locally advanced operable breast cancer: results from long-term follow-up.

机构信息

Department of Radiotherapy and Oncology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Breast Cancer. 2013 Oct;20(4):357-62. doi: 10.1007/s12282-012-0343-4. Epub 2012 Feb 22.

Abstract

BACKGROUND

Neoadjuvant chemotherapy (NACT) is being increasingly used for patients with large-size operable breast cancer. This phase 2 study of sequential NACT with gemcitabine and doxorubicin (Gem + Dox) followed by gemcitabine and cisplatin (Gem + Cis) was conducted in women with large or locally advanced breast cancer. The objectives were to evaluate the pathological complete response (pCR) rate, toxicity, pathological and genetic markers predicting response, the proportion of patients undergoing breast conservation surgery, progression-free survival (PFS) and overall survival (OS) after 5 years, and time to treatment failure (TtTF). In this manuscript, we report the long-term OS, PFS, and TtTF results.

METHODS

Female patients aged at least 18 years with large T2 (at least 3 cm) or locally advanced (T3, T4, or N2) breast carcinoma were included. Treatment consisted of 4 cycles of Gem + Dox (gemcitabine 1,200 mg/m(2) on days 1 and 8 plus doxorubicin 60 mg/m(2) on day 1 of each 21-day cycle), followed by 4 cycles of Gem + Cis (gemcitabine 1,000 mg/m(2) on days 1 and 8 plus cisplatin 70 mg/m(2) on day 1 of each 21-day cycle), and then surgery.

RESULTS

Sixty-five patients were enrolled. The pCR rate was 20%. The 5-year OS probability was 71% (95% CI 56-82%), and the 4-year PFS and TtTF probabilities were 63% (95% CI 48-74%) and 45% (95% CI 32-57%), respectively.

CONCLUSIONS

NACT with Gem + Dox followed by Gem + Cis was efficacious in patients with operable breast cancer.

摘要

背景

新辅助化疗(NACT)越来越多地用于可手术的大尺寸乳腺癌患者。本研究为Ⅱ期临床试验,旨在评估吉西他滨联合多柔比星(Gem+Dox)序贯化疗后行吉西他滨联合顺铂(Gem+Cis)新辅助化疗方案在局部晚期或大尺寸乳腺癌患者中的疗效。该方案中,65 例患者接受 4 周期 Gem+Dox(吉西他滨 1200mg/m2,第 1 天和第 8 天;多柔比星 60mg/m2,第 1 天,每 21 天为 1 周期)治疗,继以 4 周期 Gem+Cis(吉西他滨 1000mg/m2,第 1 天和第 8 天;顺铂 70mg/m2,第 1 天,每 21 天为 1 周期)治疗,随后行手术治疗。本研究报道了该方案的长期总生存(OS)、无进展生存(PFS)和治疗失败时间(TtTF)。

方法

本研究纳入年龄≥18 岁的局部晚期或大尺寸乳腺癌患者(T2 期肿瘤至少 3cm,或 T3、T4 或 N2 期)。主要研究终点为病理完全缓解率(pCR)、毒性、预测疗效的病理及遗传学标志物、保乳手术率、5 年 PFS 和 OS 以及 TtTF。

结果

共纳入 65 例患者,pCR 率为 20%。5 年 OS 率为 71%(95%CI 56%-82%),4 年 PFS 和 TtTF 率分别为 63%(95%CI 48%-74%)和 45%(95%CI 32%-57%)。

结论

对于可手术的乳腺癌患者,Gem+Dox 序贯 Gem+Cis 新辅助化疗方案有效。

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