Use of granulocyte colony-stimulating factor after high-dose chemotherapy and autologous peripheral blood stem cell transplantation - What is the optimal timing?

被引:7
作者
Ener, RA
Meglathery, SB
Cuhaci, B
Topolsky, D
Styler, MJ
Crilley, P
Brodsky, I
Kahn, SB
King, RS
机构
[1] Med Coll Penn & Hahnemann Univ, Hahnemann Univ Hosp, Div Hematol & Med Oncol, Philadelphia, PA 19102 USA
[2] Med Coll Penn & Hahnemann Univ, Hahnemann Univ Hosp, Dept Med, Div Nephrol, Philadelphia, PA 19102 USA
[3] Med Coll Penn & Hahnemann Univ, Hahnemann Univ Hosp, Div Hematol & Med Oncol, Philadelphia, PA 19102 USA
[4] Med Coll Penn & Hahnemann Univ, Hahnemann Univ Hosp, Dept Pharm, Philadelphia, PA 19102 USA
[5] Med Coll Penn Hosp, Philadelphia, PA USA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2001年 / 24卷 / 01期
关键词
granulocyte colony-stimulating factor; optimal timing; high-dose chemotherapy; autologous peripheral blood stem cell transplantation; neutrophil recovery; posttransplant hospital days; total hospital days; clinical outcomes;
D O I
10.1097/00000421-200102000-00003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Administration of granulocyte colony-stimulating factor to patients undergoing high-dose chemotherapy and autologous peripheral blood stem cell transplantation accelerates neutrophil recovery and decreases hospitalization time. The optimal timing for granulocyte colony-stimulating factor infusion remains unknown. In this retrospective, case-controlled, two-armed study, we reviewed our experience at Hahnemann University Hospital to determine whether initiating granulocyte colony-stimulating factor infusions on posttransplant day 0 versus day 8 affects neutrophil recovery time, posttransplant discharge date, total hospital days after high-dose chemotherapy, and autologous peripheral blood stem cell transplantation. All patients hospitalized between 1994 and 1998 at Hahnemann University Hospital. Bone Marrow Transplantation Unit with breast cancer or non-Hodgkin's lymphoma, who underwent high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation and received granulocyte colony-stimulating factor either on posttransplant day 0 (16 patients) or day 8 (16 patients). The day 0 and day 8 groups had no statistically significant differences in age, sex, weight, height, body surface area, disease characteristics, pretransplant harvesting or conditioning regimens, or transplant CD34(+) cell counts. Our main outcome measure was the mean time to reach absolute neutrophil count greater than or equal to 0.5 X 10(9)/1, the number of hospital days after transplant, and the total hospital days. The mean days to neutrophil recovery (10.56 versus 9.68, p = 0.48), posttransplant hospital days (13.62 versus 12.81, p = 0.39), acid total hospital days (20.25 versus 20.25. p = 1.00) were not significantly different between day 8 and day 0 groups, respectively. No significant effects on neutrophil recovery time, posttransplant hospital days, or total hospital days were observed with the initial granulocyte colony-stimulating factor infusion on day 0 versus day 8 after transplant. Delayed administration may allow substantial cost savings (US$200 X 8 congruent to US$1,600 per patient) without affecting clinical outcome. More studies are needed to determine whether greater delay is feasible.
引用
收藏
页码:19 / 25
页数:7
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