A randomized, multicenter study of G-CSF starting on day +1 vs day +5 after autologous peripheral blood progenitor cell transplantation

被引:0
作者
AM de Azevedo
M Nucci
A Maiolino
AC Vigorito
BP Simões
FJP Aranha
DG Tabak
J Voltarelli
CA de Souza
机构
[1] University Hospital,
[2] Universidade Federal do Rio de Janeiro,undefined
[3] Universidade Estadual de Campinas,undefined
[4] Universidade de São Paulo,undefined
[5] CEMO,undefined
[6] Instituto Nacional de Câncer,undefined
[7] CEMO,undefined
[8] Instituto Nacional de Câncer,undefined
来源
Bone Marrow Transplantation | 2002年 / 29卷
关键词
G-CSF; autologous; bone marrow transplant; randomized; clinical trial;
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摘要
In order to assess the effect of delaying G-CSF administration after autologous peripheral blood progenitor cell (PBPC) transplantation on the duration of neutropenia, 87 patients were randomized to receive G-CSF 5 μg/kg/day starting on day +1 (n = 45) or +5 (n = 42) following PBPC transplantation, until recovery of the neutrophils. The duration of neutropenia (<0.5 × 109/l) was shorter in the day +1 group (7 vs 8 days; P = 0.02), especially in patients receiving melphalan 200 mg/m2 and CD34+ cell doses >3.0 × 106/kg. These patients had a later onset of neutropenia after transplant. There were no differences in time to neutrophil and platelet engraftment, or in the incidence of fever and documentation of infection. Although the duration of antibiotic therapy (7 vs 10.5 days; P = 0.01) and time to hospital discharge (13 vs 15 days; P = 0.02) were shorter in the day +1 group, these differences could not be predicted by the day of G-CSF initiation in multivariate analysis. Starting G-CSF on day +1 does not result in faster neutrophil engraftment but in later onset and consequently, slightly shorter duration of neutropenia in patients who receive melphalan 200 mg/m2 and CD34+ cell doses >3.0 × 106/kg.
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页码:745 / 751
页数:6
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  • [1] Kirk JL(1998)Analysis of early infectious complications after autologous bone marrow transplantation Cancer 62 2445-2450
  • [2] Greenfield RA(1966)Quantitative relationship between circulating leukocytes and infection in patients with acute leukemia Ann Intern Med 64 328-340
  • [3] Slease RB(1996)Early infectious complications in autologous bone marrow transplantation: a review of 219 patients Bone Marrow Transplant 18 265-271
  • [4] Bodey GP(1989)Granulocyte colony-stimulating factor and neutrophil recovery after high-dose chemotherapy and autologous bone marrow transplantation Lancet 2 891-895
  • [5] Buckley M(1989)Recombinant human granulocyte colony-stimulating factor hastens granulocyte recovery after high-dose chemotherapy and autologous bone marrow transplantation in Hodgkin's disease J Clin Oncol 7 1791-1799
  • [6] Sathe YS(1994)Randomized study of recombinant human granulocyte colony-stimulating factor after high-dose chemotherapy and autologous bone marrow transplantation for high-risk lymphoid malignancies J Clin Oncol 12 1931-1938
  • [7] Mossad SB(1994)Placebo-controlled phase III trial of lenograstim in bone marrow transplantation Lancet 343 696-700
  • [8] Longworth DL(1995)G-CSF after autologous bone marrow transplantation for malignant diseases in children Bone Marrow Transplant 15 349-351
  • [9] Goormastic M(1995)Results of a randomised, controlled, multicentre study of recombinant human granulocyte colony-stimulating factor (filgrastim) in patients with Hodgkin's disease and non-Hodgkin's lymphoma undergoing autologous bone marrow transplantation Bone Marrow Transplant 15 261-266
  • [10] Sheridan WP(1995)Granulocyte colony-stimulating factor accelerates neutrophil engraftment following peripheral blood stem cell transplantation: a prospective, randomized trial J Clin Oncol 13 1323-1327