1 Haematology Directorate, SA Pathology, Adelaide, SA, Australia.
2 School of Medicine, University of Queensland, St Lucia, QLD, Australia.
Aust N Z J Psychiatry. 2017 Oct;51(10):980-989. doi: 10.1177/0004867417720516. Epub 2017 Jul 27.
Clozapine is the most effective medication for treatment-refractory schizophrenia; however, its use is contraindicated in people who have had previous clozapine-induced neutropenia. Co-prescription of granulocyte-colony stimulating factor may prevent recurrent neutropenia and allow continuation or rechallenge of clozapine.
Systematic review of literature reporting the use of granulocyte-colony stimulating factor to allow rechallenge or continuation of clozapine in people with previous episodes of clozapine-induced neutropenia. The efficacy of granulocyte-colony stimulating factor and predictors of successful rechallenge will be determined to elucidate whether evidence-based recommendations can be made regarding the use of granulocyte-colony stimulating factor in this context.
A total of 17 articles were identified that reported on clozapine rechallenge with granulocyte-colony stimulating factor support. In all, 76% of cases were able to continue clozapine at median follow-up of 12 months. There were no clear clinical or laboratory predictors of successful rechallenge; however, initial neutropenia was more severe in successful cases compared to unsuccessful cases. Cases co-prescribed lithium had lower success rates of rechallenge (60%) compared to those who were not prescribed lithium (81%). The most commonly reported rechallenge strategy was use of filgrastim 150-480 µg between daily to three times a week. There were no medication-specific side effects of granulocyte-colony stimulating factor reported apart from euphoria in one case. Three cases who failed granulocyte-colony stimulating factor had bacterial infection at time of recurrent neutropenia. No deaths were reported.
Preliminary data suggest granulocyte-colony stimulating factor is safe and effective in facilitating rechallenge with clozapine. Clinical recommendations for use are discussed.
氯氮平是治疗难治性精神分裂症最有效的药物;然而,对于曾经有过氯氮平诱导性中性粒细胞减少症的患者,其使用是禁忌的。同时使用粒细胞集落刺激因子可能预防中性粒细胞减少症的复发,并允许继续或重新使用氯氮平。
系统综述文献报告粒细胞集落刺激因子用于允许重新使用或继续使用氯氮平治疗以前有氯氮平诱导性中性粒细胞减少症发作的患者。将确定粒细胞集落刺激因子的疗效和成功重新挑战的预测因素,以阐明在这种情况下是否可以对粒细胞集落刺激因子的使用提出循证建议。
共确定了 17 篇报告粒细胞集落刺激因子支持下氯氮平重新挑战的文章。在所有情况下,中位数随访 12 个月后,76%的患者能够继续使用氯氮平。没有明确的临床或实验室预测因素来预测成功的重新挑战;然而,在成功的病例中,初始中性粒细胞减少症比不成功的病例更严重。与未开锂的患者相比(81%),同时开锂的患者(60%)重新挑战的成功率较低。最常报告的重新挑战策略是使用非格司亭 150-480μg,每天一次至每周三次。除了一例报告欣快外,没有报告粒细胞集落刺激因子的药物特异性副作用。在中性粒细胞减少症复发时,有 3 例粒细胞集落刺激因子失败的患者发生细菌感染。没有报告死亡。
初步数据表明,粒细胞集落刺激因子在促进氯氮平重新挑战方面是安全有效的。讨论了临床使用建议。