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粒细胞集落刺激因子(G-CSF)作为成人急性淋巴细胞白血病(ALL)诱导化疗的辅助用药。

Granulocyte colony-stimulating factor (G-CSF) as an adjunct to induction chemotherapy of adult acute lymphoblastic leukemia (ALL).

作者信息

Scherrer R, Geissler K, Kyrle P A, Gisslinger H, Jäger U, Bettelheim P, Laczika K, Locker G, Scholten C, Sillaber C

机构信息

Division of Hematology, First Medical Department, University of Vienna, Austria.

出版信息

Ann Hematol. 1993 Jun;66(6):283-9. doi: 10.1007/BF01695970.

Abstract

Our purpose was to evaluate the ability of recombinant human granulocyte colony-stimulating factor (r-metHuG-CSF) as an adjunct to induction chemotherapy of acute lymphoblastic leukemia (ALL) to ameliorate chemotherapy-induced neutropenia and thus allow patients to receive full doses of chemotherapy on time. Sixteen consecutive patients with adult ALL (13 de novo, three relapsed) were treated with induction chemotherapy according to the BMFT protocol and received in addition r-metHuG-CSF (200 micrograms/m2/day). Patients who were treated with the same induction chemotherapy but without G-CSF between 1982 and 1990 served as controls. Fifteen of the 16 patients achieved complete hematological remission. One patient died because of fungal septicemia. Compared with historical controls, G-CSF-treated patients had a significantly faster neutrophil recovery in phase I, resulting in neutrophil counts > 1000/microliters at day 17 vs day 26 (in median) in controls. In phase II, the onset of severe leukocytopenia (< 1500/microliters) was significantly (p = 0.01) delayed and the degree of leukocytopenia less pronounced (mean nadir 3300/microliters) in G-CSF-treated patients compared with controls (1880/microliters). The number of days of febrile neutropenia was not different in phase I. In phase II it was lower in study patients (0 vs 1.1 days), but the difference did not reach statistical significance (p = 0.09). Full doses of chemotherapy could be given on time to 11/13 (85%) G-CSF patients but to only 7/30 (23%) controls. These data indicate that (a) G-CSF can be given along with chemotherapy in induction treatment of ALL without compromising efficacy; (b) the duration of neutropenia in phase I is markedly shortened and the degree of leukocytopenia in phase II ameliorated; (c) these beneficial effects allow patients to receive full doses of chemotherapy on time.

摘要

我们的目的是评估重组人粒细胞集落刺激因子(r-metHuG-CSF)作为急性淋巴细胞白血病(ALL)诱导化疗辅助药物,改善化疗引起的中性粒细胞减少症,从而使患者能够按时接受全剂量化疗的能力。16例连续性成年ALL患者(13例初发,3例复发)按照BMFT方案接受诱导化疗,并额外接受r-metHuG-CSF(200微克/平方米/天)治疗。1982年至1990年间接受相同诱导化疗但未使用G-CSF的患者作为对照。16例患者中有15例实现了完全血液学缓解。1例患者因真菌败血症死亡。与历史对照相比,接受G-CSF治疗的患者在第一阶段中性粒细胞恢复明显更快,导致第17天中性粒细胞计数>1000/微升,而对照组中位数为第26天。在第二阶段,与对照组(1880/微升)相比,接受G-CSF治疗的患者严重白细胞减少症(<1500/微升)的发作明显延迟(p = 0.01),白细胞减少程度较轻(平均最低点3300/微升)。第一阶段发热性中性粒细胞减少症的天数没有差异。在第二阶段,研究患者的天数较低(0天对1.1天),但差异未达到统计学意义(p = 0.09)。13例接受G-CSF治疗的患者中有11例(85%)能够按时给予全剂量化疗,而对照组中只有7/30(23%)能够按时给予。这些数据表明:(a)在ALL诱导治疗中,G-CSF可与化疗同时使用而不影响疗效;(b)第一阶段中性粒细胞减少的持续时间明显缩短,第二阶段白细胞减少的程度得到改善;(c)这些有益效果使患者能够按时接受全剂量化疗。

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