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造血生长因子能否用于提高细胞毒性化疗的成功率?

Can hematopoietic growth factors be used to improve the success of cytotoxic chemotherapy?

作者信息

Bronchud M

机构信息

Department of Haematology/Oncology, Hospital of San Pablo, Barcelona, Spain.

出版信息

Anticancer Drugs. 1993 Apr;4(2):127-39. doi: 10.1097/00001813-199304000-00002.

Abstract

Hematopoietic growth factors (HGFs) have provided oncologists with powerful tools to investigate questions of chemotherapy dose and treatment outcome in cancer patients. Agents such as recombinant granulocyte colony-stimulating factor (e.g. G-CSF; filgrastim) significantly accelerate neutrophil recovery after chemotherapy and therefore allow the delivery of a planned dose on time. Moreover, it is possible to investigate the effects of escalated dose chemotherapy with HGF support. This can be done using the HGF alone or in conjunction with stem cell rescue. HGFs significantly reduce morbidity following bone marrow transplantation (BMT) and may also be used to mobilize peripheral blood progenitor cells (PBPC) to support high-dose chemotherapy. Growth factor-mobilized PBPC have practical and clinical advantages over BMT and may be a more effective method of allowing the delivery of high-dose therapy, but for some patients (who for reasons not yet clear, display a poor mobilization response) a combination of autologous bone marrow and PBPC might be more effective at reconstituting hematopoiesis. Whether more intensive treatment approaches will significantly improve survival remains to be determined.

摘要

造血生长因子(HGFs)为肿瘤学家提供了强大的工具,用以研究癌症患者化疗剂量与治疗结果相关的问题。诸如重组粒细胞集落刺激因子(如G-CSF;非格司亭)等药物可显著加速化疗后中性粒细胞的恢复,从而使按时给予计划剂量成为可能。此外,还能够研究在HGF支持下增加化疗剂量的效果。这可以单独使用HGF或与干细胞救援联合进行。HGFs可显著降低骨髓移植(BMT)后的发病率,也可用于动员外周血祖细胞(PBPC)以支持高剂量化疗。生长因子动员的PBPC相较于BMT具有实际和临床优势,可能是实现高剂量治疗的更有效方法,但对于一些患者(原因尚不清楚,动员反应较差),自体骨髓和PBPC联合使用在重建造血方面可能更有效。强化治疗方法是否会显著提高生存率仍有待确定。

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