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对于未经化疗的转移性乳腺癌,采用短疗程诱导化疗,随后进行两个周期的大剂量化疗并联合干细胞救援:序贯I/II期研究。

A short course of induction chemotherapy followed by two cycles of high-dose chemotherapy with stem cell rescue for chemotherapy naive metastatic breast cancer: sequential phase I/II studies.

作者信息

Elias A D, Richardson P, Avigan D, Ibrahim J, Joyce R, McDermott D, Levine J, Warren D, McCauley M, Wheeler C, Frei E

机构信息

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

出版信息

Bone Marrow Transplant. 2001 Sep;28(5):447-54. doi: 10.1038/sj.bmt.1703148.

Abstract

Two cycles of high-dose chemotherapy with stem cell support (HDC) may increase the total dose delivered and dose intensity. A brief induction phase and different non-cross-resistant agents for each HDC cycle were used to avoid drug resistance. Twenty-six women with metastatic BC had induction and stem cell mobilization with two cycles of doxorubicin/G-CSF given every 14 days. Patients with stable disease or better after induction received HD CTCb followed by HD melphalan and dose-escalated paclitaxel. At 475 mg/m(2) of paclitaxel by 24-h infusion, dose-limiting transient peripheral sensory neuropathy was encountered. No toxic deaths occurred. Complete and near complete response after completion of therapy was achieved in 22 (85%) of 26 patients. The median EFS was 38 months. The median OS has not yet been reached. At a median follow-up of 33 (25-43) months, actuarial EFS and OS were 54% (95% confidence interval (CI), 39-69%) and 69% (95% CI, 56-79%), respectively. This double transplant approach lasts only 14 weeks and is feasible, safe, and tolerable. Whilst selection biases may in part contribute to favorable EFS and OS, a randomized comparison of standard therapy vs double transplant in both metastatic and locally advanced breast cancer is warranted.

摘要

两个周期的高剂量化疗联合干细胞支持(HDC)可能会增加给药总量和剂量强度。采用了一个简短的诱导期,并为每个HDC周期使用不同的非交叉耐药药物以避免耐药。26例转移性乳腺癌女性患者接受诱导治疗和干细胞动员,每14天给予两个周期的阿霉素/粒细胞集落刺激因子(G-CSF)。诱导后病情稳定或好转的患者接受高剂量环磷酰胺(HD CTCb),随后是高剂量美法仑和剂量递增的紫杉醇。在以24小时输注方式给予475mg/m²紫杉醇时,出现了剂量限制性短暂性周围感觉神经病变。未发生毒性死亡。26例患者中有22例(85%)在治疗完成后达到完全缓解和接近完全缓解。中位无进展生存期(EFS)为38个月。中位总生存期(OS)尚未达到。在中位随访33(25 - 43)个月时,精算的EFS和OS分别为54%(95%置信区间(CI),39 - 69%)和69%(95%CI,56 - 79%)。这种双移植方法仅持续14周,且可行、安全且可耐受。虽然选择偏倚可能部分导致了良好的EFS和OS,但有必要对转移性和局部晚期乳腺癌的标准治疗与双移植进行随机对照比较。

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