Predictors of resistance to abiraterone acetate or enzalutamide in patients with metastatic castration-resistant prostate cancer in post-docetaxel setting: a single-center cohort study
Autor: | Eduard Vrdoljak, Davor Eterović, Tomislav Omrčen |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Oncology Male Cancer Research Abiraterone Acetate Docetaxel Single Center Cohort Studies chemistry.chemical_compound Prostate cancer 0302 clinical medicine Antineoplastic Combined Chemotherapy Protocols Pharmacology (medical) Neoplasm Metastasis Aged 80 and over Abiraterone acetate Middle Aged Prostatic Neoplasms Castration-Resistant Treatment Outcome 030220 oncology & carcinogenesis Benzamides Disease Progression Hormonal therapy Kallikreins medicine.drug Cohort study Adult medicine.medical_specialty Antineoplastic Agents 03 medical and health sciences Internal medicine Nitriles Phenylthiohydantoin medicine Enzalutamide Humans Aged Pharmacology business.industry Prostate-Specific Antigen medicine.disease Confidence interval 030104 developmental biology chemistry Drug Resistance Neoplasm abiraterone enzalutamide prostate cancer resistance Prednisone business |
Zdroj: | Anti-cancer drugs. 31(7) |
ISSN: | 1473-5741 |
Popis: | Treatment with abiraterone acetate or enzalutamide is one of the approved approaches in men with metastatic castration-resistant prostate cancer (mCRPC) in the post-docetaxel setting. However, a significant fraction of patients do not respond to treatment, and we aimed to determine their characteristics. From April 2015 to May 2019, 71 patients with mCRPC were treated with abiraterone acetate (N = 34) or enzalutamide (N = 37) at our institution. Resistance to treatment was defined as radiological or scintigraphic progression within 3 months, as documented at the first control. After a median follow-up of 14.9 months, resistance was detected in 22 patients (31%). Many of the baseline characteristics differed between responders and nonresponders but did not serve as predictors with clinically acceptable certainty. To overcome this, the resistance score was defined as the number of positive out of the following six predictors: (1) not only prostate specific antigen (PSA) progression after docetaxel (2) Eastern Cooperative Oncology Group (ECOG) performance status >1 (3) duration of metastatic disease 52 ng/mL (5) serum alkaline phosphatase >119 g/L (6) serum hemoglobin (Hb) concentration 3 positive predictors. Therefore, by using a cutoff of four positive predictors, the resistance score showed both a high sensitivity of 82% [57–96% ; 95% confidence interval (CI)] and a specificity of 88% (74–96% ; 95% CI). The proposed resistance score integrates the diagnostic performances of multiple predictors and may serve to decide which patients with mCRPC should be offered treatments other than hormonal therapy. |
Databáze: | OpenAIRE |
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