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Ancestim(r-metHuSCF)联合非格司亭和/或化疗动员 513 例动员不佳的癌症患者的血液祖细胞:法国同情用药经验。

Ancestim (r-metHuSCF) plus filgrastim and/or chemotherapy for mobilization of blood progenitors in 513 poorly mobilizing cancer patients: the French compassionate experience.

机构信息

Institut Gustave Roussy, Villejuif, France.

出版信息

Bone Marrow Transplant. 2011 Jul;46(7):936-42. doi: 10.1038/bmt.2010.231. Epub 2010 Oct 18.

Abstract

Ancestim (r-MetHuSCF) is available in France for compassionate use in patients who are candidates for high-dose chemotherapy and autologous transplantation, and who failed in previous attempts at mobilization and collection. We report here data from 513 adult patients who benefited from this program, between January 1998 and July 2007. Given with systematic premedication, ancestim was generally well tolerated, although severe but not life-threatening adverse events were reported in 12 individuals. Overall, a graft was obtained or completed for 235 patients (46%). The median number of collected CD34+ cells was 3.00 × 10(6)/kg (range: 0.03-39.50). The target threshold of 2 × 10(6) CD34+ cells/kg was reached in 161 patients (31%). Factors associated with collection were diagnosis of myeloma, no previous autologous transplant, no more than one previous failed attempt and a mobilization regimen including cytotoxic agents. A total of 207 patients (40%) proceeded to high-dose chemotherapy and autologous transplantation. The median time to reach 0.5 × 10(9)/L neutrophils and 20 × 10(9)/L platelets was 12 (6-40) and 13 (0-31) days, respectively. We conclude that a combination of ancestim with filgrastim successfully mobilized CD34+ cells in peripheral blood, and allowed adequate collection in preparation for autologous transplantation in approximately one-third of poorly mobilizing patients.

摘要

Ancestim(r-MetHuSCF)在法国可用于同情用药,适用于那些高剂量化疗和自体移植候选患者,以及那些在前几次动员和采集尝试中失败的患者。我们报告了 1998 年 1 月至 2007 年 7 月期间,513 名接受该方案治疗的成年患者的数据。在系统预处理的情况下,ancestim 通常耐受性良好,尽管有 12 名患者报告了严重但无生命威胁的不良事件。总体而言,有 235 名患者(46%)获得或完成了移植物。采集的 CD34+细胞中位数为 3.00×10(6)/kg(范围:0.03-39.50)。161 名患者(31%)达到了 2×10(6)CD34+细胞/kg 的目标阈值。与采集相关的因素包括多发性骨髓瘤诊断、无先前自体移植、无多次先前失败尝试以及包括细胞毒性药物在内的动员方案。共有 207 名患者(40%)进行了高剂量化疗和自体移植。达到中性粒细胞 0.5×10(9)/L 和血小板 20×10(9)/L 的中位时间分别为 12(6-40)和 13(0-31)天。我们得出结论,ancestim 联合粒细胞集落刺激因子成功动员了外周血中的 CD34+细胞,并在大约三分之一的动员能力较差的患者中,为自体移植做好了充分采集的准备。

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