Sawada K I, Sato N, Kohno M, Hannda H, Yasukouchi T, Tanngo M, Hirayama A, Koike T
Department of Medicine II, Hokkaido University School of Medicine, Sapporo, Japan.
Leuk Lymphoma. 1995 Dec;20(1-2):103-9. doi: 10.3109/10428199509054760.
Bone marrow toxicity is a great challenge for physicians treating patients with non-Hodgkin's lymphoma (NHL) and prescribed chemotherapy. Granulocyte colony-stimulating factor (G-CSF) prevents myelotoxicity, but the optimal timing and scheduling of G-CSF administration has not been ascertained. We investigated leukocyte count oriented G-CSF administration schedules, as related to full dose administration of cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP) chemotherapy, with shortened intervals. Thirty-eight Japanese patients with NHL were included in this study. The standard CHOP combination was administered in six cycles. Patients were given G-CSF in a dose of 2 micrograms/kg/day, subcutaneously starting the day when total leukocytes were < 3,000/microliters. When leukocyte count remained at > 3,000/microliters, G-CSF was started 10 days following CHOP. Treatment with G-CSF was discontinued after the leucocyte count reached > 10,000/microliters, and CHOP was started the next day (CHOP-G treatment; CHOP-G). Doses were not modified in any patient. Patients over 70 years of age received 2/3 of the standard dosage. In the first cycle of CHOP, the day of initiation of G-CSF was 9.6 days following CHOP in the first cycle and 7.7 to 8.5 days during 2 to 6 cycles. The mean duration of G-CSF injection was 7.4 days with a range from 6.8 to 8.0 days, in each CHOP cycle. The mean intervals of CHOP-G was 14.7 days during six consecutive courses, and there was no prolongation of the intervals, even in later cycles. In 23 patients who received all six cycles of CHOP-G, the overall response rate was 91.3% (73.9% complete remission; CR and 17.4% partial remission; PR). In 32 patients with intermediate grade NHL, the overall response rate was 84.4% (65.5% CR and 18.8% PR). Thus, the full dose CHOP with G-CSF, based on the leukocyte count oriented schedule, can be achieved with shortened intervals, an approach which will increase the quality of life (QOL) for the patients by reducing the days of treatment as well as the cost of G-CSF.
骨髓毒性对于治疗非霍奇金淋巴瘤(NHL)患者并开具化疗药物的医生而言是一项巨大挑战。粒细胞集落刺激因子(G-CSF)可预防骨髓毒性,但G-CSF给药的最佳时机和方案尚未确定。我们研究了与环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗全剂量给药相关的、间隔缩短的以白细胞计数为导向的G-CSF给药方案。本研究纳入了38例日本NHL患者。标准CHOP方案分六个周期给药。当全白细胞计数<3000/微升时,患者开始皮下注射G-CSF,剂量为2微克/千克/天。当白细胞计数保持>3000/微升时,在CHOP治疗后10天开始使用G-CSF。白细胞计数达到>10000/微升后停止使用G-CSF治疗,次日开始CHOP治疗(CHOP-G治疗;CHOP-G)。所有患者的剂量均未调整。70岁以上患者接受标准剂量的2/3。在CHOP的第一个周期中,G-CSF开始使用的时间在第一个周期为CHOP治疗后9.6天,在第2至6个周期为7.7至8.5天。在每个CHOP周期中,G-CSF注射的平均持续时间为7.4天,范围为6.8至8.0天。在连续六个疗程中,CHOP-G的平均间隔时间为14.7天,即使在后续周期中,间隔时间也没有延长。在接受了全部六个周期CHOP-G治疗的23例患者中,总缓解率为91.3%(完全缓解率;CR为73.9%,部分缓解率;PR为17.4%)。在32例中度NHL患者中,总缓解率为84.4%(CR为65.5%,PR为18.8%)。因此,基于以白细胞计数为导向的方案,全剂量CHOP联合G-CSF可在缩短间隔时间的情况下实现,这种方法将通过减少治疗天数以及G-CSF的费用来提高患者的生活质量(QOL)。