Literature DB >> 28361167

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

Clément Bonnet1, Pascaline Boudou-Rouquette1, Esther Azoulay-Rutman2, Olivier Huillard1, Jean-Louis Golmard3, Edith Carton1, Gaëlle Noé2, Michel Vidal2,4, Galdric Orvoen5, Anne Chah Wakilian5, Clémentine Villeminey1, Benoit Blanchet2, Jérôme Alexandre1, François Goldwasser1, Audrey Thomas-Schoemann6,7.   

Abstract

PURPOSE: 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.
METHODS: 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.
RESULTS: 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.
CONCLUSIONS: 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.

Entities:  

Keywords:  Abiraterone; Drug–drug interactions; Pharmacist; Prevalence; Prostate cancer

Mesh:

Substances:

Year:  2017        PMID: 28361167     DOI: 10.1007/s00280-017-3291-z

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  4 in total

1.  Prevalence of drug-drug interactions in sarcoma patients: key role of the pharmacist integration for toxicity risk management.

Authors:  Audrey Bellesoeur; Ithar Gataa; Pascaline Boudou-Rouquette; Audrey Thomas-Schoemann; Anne Jouinot; Sarah El Mershati; Anne-Catherine Piketty; Camille Tlemsani; David Balakirouchenane; Anthia Monribot; Michel Vidal; Rui Batista; Sixtine de Percin; Clémentine Villeminey; Jérôme Alexandre; François Goldwasser; Benoit Blanchet
Journal:  Cancer Chemother Pharmacol       Date:  2021-07-24       Impact factor: 3.333

2.  A clinically relevant decrease in abiraterone exposure associated with carbamazepine use in a patient with castration-resistant metastatic prostate cancer.

Authors:  Guillemette E Benoist; Maarten J van der Doelen; Rob Ter Heine; Nielka P van Erp; Niven Mehra
Journal:  Br J Clin Pharmacol       Date:  2018-02-21       Impact factor: 4.335

3.  Drug-drug interaction potential in men treated with enzalutamide: Mind the gap.

Authors:  Guillemette Emma Benoist; Inge M van Oort; Stella Smeenk; Adrian Javad; Diederik M Somford; David M Burger; Niven Mehra; Nielka P van Erp
Journal:  Br J Clin Pharmacol       Date:  2017-10-18       Impact factor: 4.335

4.  New Oral Antitumor Drugs and Medication Safety in Uro-Oncology: Implications for Clinical Practice Based on a Subgroup Analysis of the AMBORA Trial.

Authors:  Katja Schlichtig; Lisa Cuba; Pauline Dürr; Laura Bellut; Norbert Meidenbauer; Frank Kunath; Peter J Goebell; Andreas Mackensen; Frank Dörje; Martin F Fromm; Bernd Wullich
Journal:  J Clin Med       Date:  2022-08-04       Impact factor: 4.964

  4 in total

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