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转移性乳腺癌患者在接受大剂量化疗及自体造血干细胞移植后获得完全缓解可带来生存获益。

Complete response after high-dose chemotherapy and autologous hemopoietic stem cell transplatation in metastatic breast cancer results in survival benefit.

作者信息

Kurian Sobha, Qazilbash Muzzafar, Fay Joseph, Wolff S, Herzig Roger, Hobbs Gerry, Bunner Pam, Weisenborn Robin, Aya-Ay Melanie, Lynch Joseph, Ericson Solveig

机构信息

West Virginia University, Morgantown, West Virginia 26505, USA.

出版信息

Breast J. 2006 Nov-Dec;12(6):531-5. doi: 10.1111/j.1524-4741.2006.00341.x.

Abstract

Metastatic breast cancer is an incurable disease even with high-dose chemotherapy (HDC) and autologous hematopoietic stem cell transplantation (ASCT). Even though phase III studies have not shown a survival advantage for this group as a whole, it is possible that a small subset of patients may benefit from HDC/ASCT with careful patient selection. A total of 198 patients from three different institutions were treated with HDC/ASCT. After complete staging, patients with central nervous system or bone marrow involvement were excluded. The HDC regimen consisted of: Carboplatin 600 mg/m(2) IV infusion over 48 hours, Thiotepa 300 mg/m(2) IV infusion over 2 hours, and Cytoxan 60 mg/kg IV infusion given over 2 hours x3 days. The median age at the time of transplant was 46 (24-62) years and median follow-up was 20 months. Hormone receptor status was known in 148 patients, of whom 84 had estrogen receptor (ER) and/or progestrone receptor (PgR)-positive tumors. Eighty patients had no evidence of disease at the time of HDC/ASCT (CR1). At the completion of HDC and ASCT, complete responses (CR) were seen in an additional 57 patients (CR2). Using Kaplan-Meier analysis, the median relapse-free survival (RFS) for the entire group was 15 months and overall survival (OS) was 27 months. The patients in CR1 had a median RFS and OS of 20.7 and 50.6 months, respectively. This was very similar to the RFS and OS in patients achieving CR2 after HDC/ASCT (p < 0.001; median: 19 and 40 months, respectively). In contrast, the patients with persistent residual disease had an RFS and OS of 7 and 12 months (p < 0.001). These data show that patients achieving a CR after HDC/ASCT have a better relapse-free and OS, when compared to patients with persistent residual disease after HDC/ASCT. This study suggests that a subset of patients with residual metastatic breast cancer after standard chemotherapy can achieve CR with HDC and ASCT which may result in better long-term outcome.

摘要

转移性乳腺癌即使采用大剂量化疗(HDC)和自体造血干细胞移植(ASCT)也是一种无法治愈的疾病。尽管III期研究尚未显示该组患者总体有生存优势,但通过仔细挑选患者,一小部分患者可能会从HDC/ASCT中获益。来自三个不同机构的198例患者接受了HDC/ASCT治疗。在完成全面分期后,排除有中枢神经系统或骨髓受累的患者。HDC方案包括:卡铂600mg/m²静脉输注48小时,噻替派300mg/m²静脉输注2小时,环磷酰胺60mg/kg静脉输注2小时,共3天。移植时的中位年龄为46(24 - 62)岁,中位随访时间为20个月。148例患者的激素受体状态已知,其中84例患者的肿瘤为雌激素受体(ER)和/或孕激素受体(PgR)阳性。80例患者在接受HDC/ASCT时无疾病证据(CR1)。在HDC和ASCT完成时,另外57例患者出现完全缓解(CR2)。使用Kaplan-Meier分析,整个组的中位无复发生存期(RFS)为15个月,总生存期(OS)为27个月。CR1组患者的中位RFS和OS分别为20.7个月和50.6个月。这与HDC/ASCT后达到CR2的患者的RFS和OS非常相似(p < 0.001;中位值分别为19个月和40个月)。相比之下,有持续性残留疾病的患者的RFS和OS分别为7个月和12个月(p < 0.001)。这些数据表明,与HDC/ASCT后有持续性残留疾病的患者相比,HDC/ASCT后达到CR的患者有更好的无复发生存期和总生存期。这项研究表明,标准化疗后有残留转移性乳腺癌的一部分患者可以通过HDC和ASCT达到CR,这可能会带来更好的长期结果。

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