The Use of Granulocyte Colony-Stimulating Factor in Clozapine Rechallenge A Systematic Review

被引:27
|
作者
Lally, John [1 ,2 ,3 ]
Malik, Steffi [4 ]
Krivoy, Amir [1 ,5 ]
Whiskey, Eromona [5 ,6 ]
Taylor, David M. [5 ,6 ,7 ]
Gaughran, Fiona P. [1 ,5 ]
Flanagan, Robert J. [1 ]
Mijovic, Aleksandar [8 ]
MacCabe, James H. [1 ,5 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, PO63,De Crespigny Pk, London SE5 8AF, England
[2] Beaumont Hosp, Royal Coll Surg Ireland, Dept Psychiat, Dublin, Ireland
[3] Univ Coll Dublin, St Vincents Univ Hosp, Sch Med & Med Sci, Dept Psychiat, Dublin, Ireland
[4] Univ Bristol, Sch Med, Bristol, Avon, England
[5] South London & Maudsley NHS Fdn Trust, Natl Psychosis Serv, London, England
[6] South London & Maudsley NHS Fdn Trust, Pharm Dept, London, England
[7] Kings Coll London, Inst Pharmaceut Sci, London, England
[8] Kings Coll Hosp London, Dept Haematol Med, London, England
关键词
granulocyte colony-stimulating factors; G-CSF; GM-CSF; treatment-resistant; schizophrenia; clozapine; neutropenia; agranulocytosis; FACTOR G-CSF; TREATMENT-RESISTANT SCHIZOPHRENIA; TERM COMBINATION TREATMENT; NEUTROPENIA; PATIENT; FILGRASTIM;
D O I
10.1097/JCP.0000000000000767
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose/Background: Clozapine is associated with hematological abnormalities, with neutropenia and agranulocytosis of most concern. Granulocyte colony-stimulating factor (G-CSF) has been used to support clozapine rechallenge after neutropenia with the aim of maintaining the neutrophil count. This study aims to explore the practice, use, safety, and efficacy of G-CSF in this context. Methods/Procedures: We conducted a systematic review to identify all studies investigating or describing G-CSF as a prophylaxis to enable continued clozapine treatment during a rechallenge. Findings/Results: We identified 32 reports of patients who received G-CSF either regularly (n = 23) or as required (n = 9) to support clozapine rechallenge after an episode of neutropenia necessitating discontinuation of clozapine. Seventy-five percent (n = 24) of published cases remained on clozapine with the use of continual prophylactic G-CSF or after single G-CSF administrations (n = 8). Seventy percent (n = 16) of patients in receipt of continual prophylactic G-CSF were successfully maintained on clozapine. However, 1 of the 3 episodes of rechallenge in those with a history of severe agranulocytosis (absolute neutrophil count <0.1 x 10(9)/L) had a recurrence of agranulocytosis at week 9. Implications/Conclusions: Our findings suggest that G-CSF can sometimes be safely used to support the maintenance of normal neutrophil counts and clozapine use after neutropenia. Publication bias is an important limitation, however. Also, few reports clearly documented the presence or absence of an independent nonclozapine cause of the index neutropenia, which may have increased success rates. Furthermore, adverse events were not systematically recorded. Prospective studies are needed to determine safety because if agranulocytosis occurs on clozapine while supported by G-CSF, there is no obvious alternate rescue therapy to promote granulopoiesis. From the available data, it is not possible to recommend this course of action for someone with a true clozapine agranulocytosis.
引用
收藏
页码:600 / 604
页数:5
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