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囊性纤维化跨膜传导调节因子(CFTR)调节剂药物脱敏:保留长期改善的希望。

CFTR modulator drug desensitization: Preserving the hope of long term improvement.

作者信息

Leonhardt Kelsey, Autry Elizabeth B, Kuhn Robert J, Wurth Mark A

机构信息

Department of Pharmacy Services, University of Kentucky HealthCare, Lexington, Kentucky, USA.

Department of Pharmacy Practice and Sciences, University of Kentucky College of Pharmacy, Lexington, Kentucky, USA.

出版信息

Pediatr Pulmonol. 2021 Aug;56(8):2546-2552. doi: 10.1002/ppul.25437. Epub 2021 May 3.

Abstract

The development of modulator therapy has, for the first time, allowed direct targeting of the underlying cause of cystic fibrosis (CF), the cystic fibrosis transmembrane conductance regulator (CFTR). Patients treated with CFTR modulators have improvement in lung function and decreased rates of pulmonary exacerbations. In 2019, elexacaftor/tezacaftor/ivacaftor was approved for use in the United States, opening these therapies to 90% of patients with CF. Intolerable adverse drug reactions to CFTR modulators results in discontinuation of therapy, which can be devastating to our patients. We describe our approach to two cases, not previously reported, of rash to elexacaftor/tezacaftor/ivacaftor in patients with a previous history of cutaneous adverse reactions to dual modulator therapy that had been addressed by desensitization. Case 1 was able to tolerate elexacaftor/tezacaftor/ivacaftor after desensitization to the triple combination therapy, while in Case 2 tolerance was obtained by treating through the reaction. The loss of tolerance in these patients was unexpected, and may be a common finding in patients with history of cutaneous adverse reactions to these drugs. We hope reporting our experience, including our desensitization protocol, may benefit CF patients for whom these drug reactions may be limiting access to powerful disease altering therapies.

摘要

调节剂疗法的发展首次实现了直接针对囊性纤维化(CF)的根本病因——囊性纤维化跨膜传导调节因子(CFTR)进行治疗。接受CFTR调节剂治疗的患者肺功能得到改善,肺部恶化率降低。2019年,依列卡托/替扎卡托/依伐卡托在美国获批使用,使90%的CF患者能够接受这些疗法。对CFTR调节剂产生无法耐受的药物不良反应会导致治疗中断,这对我们的患者可能是灾难性的。我们描述了我们对两例此前未报道过的病例的处理方法,这两例患者对依列卡托/替扎卡托/依伐卡托出现皮疹,他们既往有过对双重调节剂疗法的皮肤不良反应史,之前通过脱敏处理过。病例1在对三联组合疗法进行脱敏后能够耐受依列卡托/替扎卡托/依伐卡托,而病例2通过在反应期间继续治疗获得了耐受性。这些患者耐受性的丧失出乎意料,可能在有这些药物皮肤不良反应史的患者中很常见。我们希望报告我们的经验,包括我们的脱敏方案,可能会使那些药物反应可能限制其获得强效疾病改变疗法的CF患者受益。

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