Potential drug-drug interactions with abiraterone in metastatic castration-resistant prostate cancer patients: a prevalence study in France

被引:18
作者
Bonnet, Clement [1 ]
Boudou-Rouquette, Pascaline [1 ]
Azoulay-Rutman, Esther [2 ]
Huillard, Olivier [1 ]
Golmard, Jean-Louis [3 ]
Carton, Edith [1 ]
Noe, Gaelle [2 ]
Vidal, Michel [2 ,4 ]
Orvoen, Galdric [5 ]
Wakilian, Anne Chah [5 ]
Villeminey, Clementine [1 ]
Blanchet, Benoit [2 ]
Alexandre, Jerome [1 ]
Goldwasser, Francois [1 ]
Thomas-Schoemann, Audrey [2 ,4 ]
机构
[1] Hop Cochin, AP HP, Serv Cancerol Med, Paris, France
[2] Hop Cochin, AP HP, Unite Fonct Pharmacocinet & Pharmacochim, Paris, France
[3] Hop La Pitie Salpetriere, AP HP, Dept Biostat, Paris, France
[4] Univ Paris 05, PRES Sorbonne Paris Cite, UFR Pharm, UMR8638,CNRS, Paris, France
[5] Univ Paris 05, Hop Broca, Hop Paris Ctr, Serv Geriatrie, Paris, France
关键词
Abiraterone; Drug-drug interactions; Prevalence; Prostate cancer; Pharmacist; PHARMACOKINETICS; POLYPHARMACY; CHEMOTHERAPY; MANAGEMENT; ACETATE; AGENTS;
D O I
10.1007/s00280-017-3291-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Abiraterone acetate combined with prednisone improves survival in metastatic castration-resistant prostate cancer (mCRPC) patients. This oral anticancer agent may result in drug-drug interactions (DDI). We aimed to evaluate the prevalence of DDI with abiraterone and the possible determinants for the occurrence of these DDI. We performed a single centre retrospective review from electronic medical records of mCRPC patients treated with abiraterone from 2011 to 2015. Potential DDI with abiraterone were identified using Micromedex and were categorized by a 4-point scale severity. Seventy-two out of ninety-five mCRPC pts (median age: 77 years [68-82]) had comorbidities. The median number of drugs used per patient was 7 [5-9]. 66 potential DDI with abiraterone were detected in 49 patients (52%): 39 and 61% were classified as major and moderate DDI, respectively. In the univariate analysis, pain (p < 0.0001), hypo-albuminemia (p = 0.032), and higher ECOG performance status (PS) (p = 0.013) were significantly associated with a higher risk of DDI with abiraterone. Pain (p < 0.0001) and PS (p = 0.018) remained significant in the multivariate analysis. Polypharmacy is an issue among mCRPC patients. In our study, half of the patients have potential DDI with abiraterone. Patients with pain and poor PS are at higher risk of DDI with abiraterone. A medication review by a pharmacist is of crucial importance to prevent DDI with abiraterone.
引用
收藏
页码:1051 / 1055
页数:5
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