Drings P, Fischer J R
Thoraxklinik, LVA Baden, Heidelberg-Rohrbach, Federal Republic of Germany.
Lung. 1990;168 Suppl:1059-68. doi: 10.1007/BF02718244.
Administration of granulocyte macrophage colony-stimulating factor (GM-CSF) has been shown to induce an increase in production of neutrophils, monocytes, and eosinophils. This is reflected in an accelerated recovery of myelopoiesis following cytotoxic chemotherapy and radiation. Human trials completed so far have used patients with many tumor types. It was clearly demonstrated that the leukocyte responses are dose and schedule dependent and that the route of factor administration is important. The results of clinical trials suggest that the acute toxicity of cytotoxic chemotherapy may be decreased. This may result in a higher dose of drugs or in a reduction of treatment interval, and it may increase the rate of complete remissions and the number of patients with long-term disease free survival, particularly in small cell lung cancer. However, up to now a definitive statement as to the value of this supportive treatment in solid tumor chemotherapy is not possible.
粒细胞巨噬细胞集落刺激因子(GM-CSF)的应用已被证明可诱导中性粒细胞、单核细胞和嗜酸性粒细胞的生成增加。这体现在细胞毒性化疗和放疗后骨髓生成的加速恢复上。迄今为止完成的人体试验涉及多种肿瘤类型的患者。已明确表明白细胞反应取决于剂量和给药方案,且因子的给药途径也很重要。临床试验结果表明,细胞毒性化疗的急性毒性可能会降低。这可能导致更高剂量的药物使用或治疗间隔的缩短,并且可能提高完全缓解率以及长期无病生存患者的数量,尤其是在小细胞肺癌中。然而,到目前为止,关于这种支持性治疗在实体瘤化疗中的价值还无法给出明确的定论。