Clinical practice and future needs in recombinant human granulocyte colony-stimulating factor treatment: a review of randomized trials in clinical haemato-oncology

被引:11
作者
Johnsen, HE [1 ]
机构
[1] Univ Copenhagen, Herlev Hosp, Dept Haematol, Stem Cell Lab, DK-2730 Herlev, Denmark
关键词
rHuG-CSF; randomized trials; haemato-oncology; febrile neutropenia; chemotherapy;
D O I
10.1177/147323000102900205
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recombinant human granulocyte colony-stimulating factor (rHuG-CSF) may have a significant impact on preventing infections associated with chemotherapy-induced neutropenia, as well as shortening time to tree lineage engraftment following high-dose chemotherapy and progenitor transplantation. However, the scientific literature documenting evidence-based practice is insufficient and often misinterpreted. This review presents data and discusses the evidence for actual clinical practice in the use of rHuG-CSF in conventional cyclic chemotherapy, either prophylactic or therapeutic, and high-dose therapy, either in priming for mobilization or post-transplantation. In the past decade, many reports have based their conclusions on surrogate markers, and it is time to move towards evaluation of clinically relevant factors. Data must be generated prospectively based on current clinical practice, and several issues must be considered and evaluated to define the true clinical benefit of rHuG-CSF with or without stem-cell support. Evaluation should include complications and needs for resources as well as impact on toxicity and efficacy of conventional or high-dose chemotherapy.
引用
收藏
页码:87 / 99
页数:13
相关论文
共 76 条
[1]  
[Anonymous], 1996, J CLIN ONCOL, V14, P1957
[2]  
[Anonymous], 1994, J CLIN ONCOL, V12, P2471
[3]   Molecular analysis of the granulocyte colony-stimulating factor receptor [J].
Avalos, BR .
BLOOD, 1996, 88 (03) :761-777
[4]   Rapid hematopoietic recovery after multicycle high-dose chemotherapy: Enhancement of filgrastim-induced progenitor-cell mobilization by recombinant human stem-cell factor [J].
Basser, RL ;
To, LB ;
Begley, CG ;
Maher, D ;
Juttner, C ;
Cebon, J ;
Mansfield, R ;
Olver, I ;
Duggan, G ;
Szer, J ;
Collins, J ;
Schwartz, B ;
Marty, J ;
Menchaca, D ;
Sheridan, WP ;
Fox, RM ;
Green, MD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (05) :1899-1908
[5]   A randomized trial of granulocyte colony-stimulating factor (Neupogen) starting day 1 vs day 7 post-autologous stem cell transplantation [J].
Bence-Bruckler, I ;
Bredeson, C ;
Atkins, H ;
McDiarmid, S ;
Hamelin, L ;
Hopkins, H ;
Perry, G ;
Genest, P ;
Huebsch, L .
BONE MARROW TRANSPLANTATION, 1998, 22 (10) :965-969
[6]   Use of hematopoietic colony-stimulating factors: Comparison of the 1994 and 1997 American Society of Clinical Oncology surveys regarding ASCO clinical practice guidelines [J].
Bennett, CL ;
Weeks, JA ;
Somerfield, MR ;
Feinglass, J ;
Smith, TJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (11) :3676-3681
[7]   HEMATOPOIETIC RESCUE AFTER HIGH-DOSE CHEMOTHERAPY USING AUTOLOGOUS PERIPHERAL-BLOOD PROGENITOR CELLS OR BONE-MARROW - A RANDOMIZED COMPARISON [J].
BEYER, J ;
SCHWELLA, N ;
ZINGSEM, J ;
STROHSCHEER, I ;
SCHWANER, I ;
OETTLE, H ;
SERKE, S ;
HUHN, D ;
SIEGERT, W .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (06) :1328-1335
[8]   LENOGRASTIM PREVENTS MORBIDITY FROM INTENSIVE INDUCTION CHEMOTHERAPY IN THE TREATMENT OF INFLAMMATORY BREAST-CANCER [J].
CHEVALLIER, B ;
CHOLLET, P ;
MERROUCHE, Y ;
ROCHE, H ;
FUMOLEAU, P ;
KERBRAT, P ;
GENOT, Y ;
FARGEOT, P ;
OLIVIER, JP ;
FIZAMES, C ;
CLAVEL, M ;
YVER, A ;
CHABERNAUD, VC .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (07) :1564-1571
[9]   REDUCTION BY GRANULOCYTE COLONY-STIMULATING FACTOR OF FEVER AND NEUTROPENIA INDUCED BY CHEMOTHERAPY IN PATIENTS WITH SMALL-CELL LUNG-CANCER [J].
CRAWFORD, J ;
OZER, H ;
STOLLER, R ;
JOHNSON, D ;
LYMAN, G ;
TABBARA, I ;
KRIS, M ;
GROUS, J ;
PICOZZI, V ;
RAUSCH, G ;
SMITH, R ;
GRADISHAR, W ;
YAHANDA, A ;
VINCENT, M ;
STEWART, M ;
GLASPY, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (03) :164-170
[10]  
Damiani D, 1997, BLOOD, V90, P36