首页> 外文期刊>Leukemia and lymphoma >Stem cell mobilization chemotherapy with gemcitabine is effective and safe in myeloma patients with bortezomib-induced neurotoxicity
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Stem cell mobilization chemotherapy with gemcitabine is effective and safe in myeloma patients with bortezomib-induced neurotoxicity

机译:吉西他滨干细胞动员化疗对硼替佐米引起的神经毒性骨髓瘤患者有效且安全

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Vinorelbine chemotherapy with granulocyte-colony stimulating factor (G-CSF) stimulation is a widely applied non-myelosuppressive mobilization regimen in Switzerland for myeloma patients, but its neurotoxic potential limits its use in patients with bortezomib-induced polyneuropathy. In this single-center study, we alternatively evaluated safety and effectiveness of gemcitabine chemotherapy with G-CSF for mobilization of autologous stem cells. Between March 2012 and February 2013, all bortezomib-pretreated myeloma patients planned to undergo first-line high-dose melphalan chemotherapy received a single dose of 1250mg/m(2) gemcitabine, with G-CSF started on day 4. The 24 patients in this study had received a median of four cycles of bortezomib-dexamethason-based induction. Bortezomib-related polyneuropathy was identified in 21 patients (88%) by clinical evaluation and a standardized questionnaire. Administration of gemcitabine mobilization did not induce new or aggravate pre-existing neuropathy. Stem cell mobilization was successful in all 24 patients, with a single day of apheresis being sufficient in 19 patients (78%). The median yield was 9.51x10(6) CD34+ cells/kg. Stem collection could be accomplished at day 8 in 67%. Our data suggest that single-dose gemcitabine together with G-CSF is an effective mobilization regimen in myeloma patients and a safe alternative non-myelosuppressive mobilization chemotherapy for myeloma patients with bortezomib-induced polyneuropathy.
机译:长春瑞滨联合粒细胞集落刺激因子(G-CSF)刺激化疗是一种广泛使用的非骨髓抑制动员疗法,在瑞士用于骨髓瘤患者,但其神经毒性潜力限制了它​​在硼替佐米引起的多发性神经病患者中的应用。在这项单中心研究中,我们另选了吉西他滨联合G-CSF进行自体干细胞动员的安全性和有效性。在2012年3月至2013年2月期间,所有计划接受一线高剂量美法仑化疗的硼替佐米治疗的骨髓瘤患者均接受1250mg / m(2)吉西他滨单剂量治疗,并于第4天开始使用G-CSF。24名患者这项研究的中位数是基于硼替佐米-地塞米松的四个周期的诱导。通过临床评估和标准化问卷,在21例患者(88%)中发现了硼替佐米相关的多发性神经病。吉西他滨动员的给药未引起新的或加重先前存在的神经病。在所有24例患者中,干细胞动员成功,其中19例(78%)的单日采血就足够了。中位数产量为9.51x10(6)CD34 +细胞/ kg。可以在第8天完成67%的茎收集。我们的数据表明,单剂量吉西他滨联合G-CSF在骨髓瘤患者中是一种有效的动员方案,对于患有硼替佐米引起的多发性神经病的骨髓瘤患者是一种安全的替代性非骨髓抑制性动员化疗。

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