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高剂量化疗后回输选择的CD34+外周血细胞用于预后不良乳腺癌患者:一项随机多中心研究

High-dose chemotherapy followed by reinfusion of selected CD34+ peripheral blood cells in patients with poor-prognosis breast cancer: a randomized multicentre study.

作者信息

Chabannon C, Cornetta K, Lotz J P, Rosenfeld C, Shlomchik M, Yanovitch S, Marolleau J P, Sledge G, Novakovitch G, Srour E F, Burtness B, Camerlo J, Gravis G, Lee-Fischer J, Faucher C, Chabbert I, Krause D, Maraninchi D, Mills B, Kunkel L, Oldham F, Blaise D, Viens P

机构信息

Institut Paoli-Calmettes, Marseilles, France.

出版信息

Br J Cancer. 1998 Oct;78(7):913-21. doi: 10.1038/bjc.1998.601.

DOI:10.1038/bjc.1998.601
PMID:9764583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2063121/
Abstract

Seventy-one patients with poor-prognosis breast cancer were enrolled after informed consent in a multicentre randomized study to evaluate the use of selected peripheral blood CD34+ cells to support haematopoietic recovery following high-dose chemotherapy. Patients who responded to conventional chemotherapy were mobilized with chemotherapy (mainly high-dose cyclophosphamide) and/or recombinant human granulocyte colony-stimulating factor (rhG-CSF). Patients who reached the threshold of 20 CD34+ cells per microl of peripheral blood underwent apheresis and were randomized at that time to receive either unmanipulated mobilized blood cells or selected CD34+ cells. For patients in the study arm, CD34+ cells were selected from aphereses using the Isolex300 device. Fifteen patients failed to mobilize peripheral blood progenitors and nine other patients were excluded for various reasons. Forty-seven eligible patients were randomized into two comparable groups. CD34+ cells were selected from aphereses in the study group. Haematopoietic recovery occurred at similar times in both groups. No side-effect related to the infusion of selected cells was observed. The frequency of epithelial tumour cells in aphereses was low (8 out of 42 evaluated patients), as determined by immunocytochemistry. We conclude that selected CD34+ cells safely support haematopoietic recovery following high-dose chemotherapy in patients with poor-prognosis breast cancer.

摘要

71例预后不良的乳腺癌患者在签署知情同意书后,被纳入一项多中心随机研究,以评估使用选定的外周血CD34+细胞来支持大剂量化疗后造血功能恢复的效果。对传统化疗有反应的患者,采用化疗(主要是大剂量环磷酰胺)和/或重组人粒细胞集落刺激因子(rhG-CSF)进行动员。外周血每微升CD34+细胞达到20个阈值的患者接受单采,并在此时随机分组,分别接受未处理的动员血细胞或选定的CD34+细胞。对于研究组的患者,使用Isolex300设备从单采物中筛选CD34+细胞。15例患者未能动员外周血祖细胞,另有9例患者因各种原因被排除。47例符合条件的患者被随机分为两个可比组。研究组从单采物中筛选CD34+细胞。两组造血功能恢复时间相似。未观察到与输注选定细胞相关的副作用。通过免疫细胞化学测定,单采物中上皮肿瘤细胞的频率较低(42例评估患者中有8例)。我们得出结论,选定的CD34+细胞能安全地支持预后不良的乳腺癌患者在大剂量化疗后造血功能的恢复。

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High-dose chemotherapy followed by reinfusion of selected CD34+ peripheral blood cells in patients with poor-prognosis breast cancer: a randomized multicentre study.高剂量化疗后回输选择的CD34+外周血细胞用于预后不良乳腺癌患者:一项随机多中心研究
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Mobilization of hematopoietic progenitor cells with paclitaxel (taxol) as a single chemotheraupetic agent, associated with rhG-CSF.以紫杉醇(泰素)作为单一化疗药物并联合重组人粒细胞集落刺激因子动员造血祖细胞。
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