Real-world outcomes of abiraterone and enzalutamide in first-line treatment of metastatic castration-resistant prostate cancer: which patients benefit most?

被引:1
|
作者
Garcia Trevijano Cabetas, Macarena [1 ]
Escario-Gomez, Miguel [1 ]
Gonzalez-Del Valle, Luis [1 ]
Sobrino Jimenez, Carmen [1 ]
Bilbao Gomez-Martino, Cristina [1 ]
Romero-Garrido, Jose Antonio [1 ]
Benedi-Gonzalez, Juana [2 ]
Espinosa Arranz, Enrique [3 ]
Diaz Almiron, Mariana [4 ]
Herrero Ambrosio, Alicia [1 ]
机构
[1] La Paz Univ Hosp, Hosp Pharm Dept, Madrid 28046, Spain
[2] Univ Complutense Madrid, Pharm Dept, Comunidad De Madrid, Spain
[3] La Paz Univ Hosp, Med Oncol Dept, Madrid, Spain
[4] La Paz Univ Hosp, Hosp Stat Dept, Madrid, Spain
关键词
medical oncology; pharmacy service; hospital; urology; statistics; urogenital system; EARLY PSA RESPONSE; PLUS PREDNISONE; ANTIGEN DECLINE; SURVIVAL; ACETATE; MEN; DOCETAXEL; MITOXANTRONE; NOMOGRAM; PREDICTS;
D O I
10.1136/ejhpharm-2021-002798
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives Abiraterone and enzalutamide are two oral novel androgen receptor axis-targeted agents approved for the treatment of castration-resistant prostate cancer (mCRPC). Despite the availability of multiple treatments, there is a need to improve the knowledge and management of these drugs in the real-world setting, especially in patient groups under-represented in clinical trials. Our aim was to review the outcome of patients with chemotherapy-naive mCRPC treated with abiraterone or enzalutamide in routine clinical practice in order to identify factors that are predictive for response. Methods This observational retrospective study was performed in a Spanish tertiary hospital and included men with chemotherapy-naive mCPRC who started treatment with abiraterone or enzalutamide between September 2012 and November 2018. The study end date was 30 October 2020. Results Ninety patients with mCRPC were included, 57 with abiraterone and 33 with enzalutamide. Median overall survival (OS) was 26.87 months (95% CI 19.68 to 34.05), with no difference found between the two treatment groups. Nine variables were related to increased OS in the univariate analysis: Eastern Cooperative Oncology Group (ECOG) performance status (0-1 vs 2), pain (need of opioids for cancer pain), visceral disease, >= 3 bone lesions, exclusively lymph node metastases, baseline prostate specific antigen (PSA) (<50 vs >= 50 ng/dL and <20 vs >= 20 ng/dL), haemoglobin (<12 vs >= 12 g/dL) and alkaline phosphatase (<= 116 vs >116 IU/L). A PSA response >50% was observed in 65 patients (76.5%). In the multivariate analysis, ECOG performance status, pain, visceral disease and alkaline phosphatase provided independent prognostic information. Median OS by Kaplan-Meier analysis was significantly longer for patients with a PSA response (32.1 vs 17.9 months; HR 0.46, 95% CI 0.27 to 0.78; p=0.003). Conclusions This study assessed the efficacy of abiraterone and enzalutamide in a real-world setting, including patients under-represented in pivotal studies. Some clinical factors were correlated with improved OS in chemotherapy-naive men with mCPRC treated with these drugs.
引用
收藏
页码:268 / 272
页数:5
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