Pharmacologic rationale for early G-CSF prophylaxis in cancer patients and role of pharmacogenetics in treatment optimization

被引:24
作者
Crea, Francesco [1 ,2 ]
Giovannetti, Elisa [1 ]
Zinzani, Pier Luigi [3 ]
Danesi, Romano [1 ]
机构
[1] Univ Pisa, Div Pharmacol & Chemotherapy, Dept Internal Med, I-56126 Pisa, Italy
[2] Scuola Super Sant Anna, Pisa, Italy
[3] Univ Bologna, L & A Seragnoli Inst Hematol & Oncol, Bologna, Italy
关键词
G-CSF; G-CSF receptor; Signalling pathways; Proliferation; Cytotoxic chemotherapy; Neutropenia; Bone marrow; Cellular compartments; Pharmacogenetics; COLONY-STIMULATING-FACTOR; ACUTE MYELOID-LEUKEMIA; MANNOSE-BINDING LECTIN; SEVERE CHRONIC NEUTROPENIA; SINGLE-NUCLEOTIDE POLYMORPHISM; DISTINCT CYTOPLASMIC REGIONS; INDUCED FEBRILE NEUTROPENIA; 3-WEEKLY CHOP CHEMOTHERAPY; HEMATOPOIETIC STEM-CELLS; HIGH-DOSE CHEMOTHERAPY;
D O I
10.1016/j.critrevonc.2008.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The use of recombinant human granulocyte colony stimulating factors (G-CSF) has become an integral part of supportive care during cytotoxic chemotherapy. Current guidelines recommend the use of G-CSF in patients with substantial risk of febrile neutropenia. However, little consensus exists about optimal timing and tailoring of this therapy. Based on the known effects of chemotherapy and G-CSF on bone marrow compartments, we propose a model that supports the prophylactic rather than therapeutic use of G-CSF therapy. In addition, several genetic alterations in G-CSF signalling pathway have been described. These genetic variants may predict the risk of febrile neutropenia and response to G-CSF Thus, future pharmacogenetic/ornics studies in this field are warranted. Through the identification of patients at risk and the knowledge of biological basis for optimal timing, hopefully we should soon be able to improve the application of the existing guidelines for G-CSF therapy and patient's prognosis. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 44
页数:24
相关论文
共 211 条
[1]   A road map for those who don't know JAK-STAT [J].
Aaronson, DS ;
Horvath, CM .
SCIENCE, 2002, 296 (5573) :1653-1655
[2]   Receptor activation and 2 distinct COOH-terminal motifs control G-CSF receptor distribution and internalization kinetics [J].
Aarts, LHJ ;
Roovers, O ;
Ward, AC ;
Touw, IP .
BLOOD, 2004, 103 (02) :571-579
[3]  
Adams Jared R, 2002, Expert Opin Pharmacother, V3, P1273
[4]   Cancer mortality in the united states by education level and race [J].
Albano, Jessica D. ;
Ward, Elizabeth ;
Jemal, Ahmedin ;
Anderson, Robert ;
Cokkinides, Vilma E. ;
Murray, Taylor ;
Henley, Jane ;
Liff, Jonathan ;
Thun, Michael J. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (18) :1384-1394
[5]  
[Anonymous], 1994, J CLIN ONCOL, V12, P2471
[6]  
[Anonymous], 1942, SOUTH MED J
[7]  
AVALOS BR, 1990, BLOOD, V75, P851
[8]   Molecular analysis of the granulocyte colony-stimulating factor receptor [J].
Avalos, BR .
BLOOD, 1996, 88 (03) :761-777
[9]   Novel variant isoform of G-CSF receptor involved in induction of proliferation of FDCP-2 cells: Relevance to the pathogenesis of myelodysplastic syndrome [J].
Awaya, N ;
Uchida, H ;
Miyakawa, Y ;
Kinjo, K ;
Matsushita, H ;
Nakajima, H ;
Ikeda, Y ;
Kizaki, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 2002, 191 (03) :327-335
[10]   Regulation of myeloid development and function by colony stimulating factors [J].
Barreda, DR ;
Hanington, PC ;
Belosevic, M .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2004, 28 (05) :509-554