Long-Term Antitumor Activity and Safety of Enzalutamide Monotherapy in Hormone Naïve Prostate Cancer: 3-Year Open Label Followup Results
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu klinické zkoušky, fáze II, časopisecké články, multicentrická studie
PubMed
28867562
DOI
10.1016/j.juro.2017.08.103
PII: S0022-5347(17)77422-8
Knihovny.cz E-zdroje
- Klíčová slova
- MDV 3100, bone density, drug related side effects and adverse reactions, prostate-specific antigen, prostatic neoplasms,
- MeSH
- aplikace orální MeSH
- benzamidy MeSH
- fenylthiohydantoin škodlivé účinky analogy a deriváty terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory prostaty farmakoterapie MeSH
- následné studie MeSH
- nitrily MeSH
- protinádorové látky škodlivé účinky terapeutické užití MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- výsledek terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze II MeSH
- multicentrická studie MeSH
- Názvy látek
- benzamidy MeSH
- enzalutamide MeSH Prohlížeč
- fenylthiohydantoin MeSH
- nitrily MeSH
- protinádorové látky MeSH
PURPOSE: A phase 2 study of enzalutamide monotherapy in patients with hormone naïve prostate cancer demonstrated high prostate specific antigen response rates at 25 weeks, 1 year and 2 years with minimal effects on total body bone mineral density and favorable safety. In this followup analysis we evaluated enzalutamide antitumor activity and safety at 3 years. MATERIALS AND METHODS: In a single arm analysis 67 patients with hormone naïve prostate cancer and noncastrate testosterone (230 ng/dl or greater) received enzalutamide 160 mg per day orally until disease progression or unacceptable toxicity. The primary end point was the prostate specific antigen response (80% or greater decline from baseline). RESULTS: No patients discontinued treatment during year 3. Of 42 patients with prostate specific antigen assessments at 3 years 38 (90.5%, 95% CI 77.4-97.3) maintained a prostate specific antigen response. Of 26 patients with metastases at baseline 17 (65.4%) had a complete or partial response as the best overall response during 3 years. In patients who completed the 3-year visit minimal mean changes from baseline were observed in total body bone mineral density or bone mineral density of the femoral neck, trochanter, spine L1-L4 or forearm (range -2.7% to -0.1%). At 3 years total body fat had increased a mean of 16.5%, total lean body mass had decreased a mean of -6.5% and global health status had minimally decreased from baseline. Common adverse events were gynecomastia, fatigue, hot flush and nipple pain. CONCLUSIONS: Enzalutamide antitumor activity was maintained in patients with hormone naïve prostate cancer at 3 years. Overall bone mineral density, global health status and safety results were similar to those at 2 years.
Aarhus University Hospital Aarhus Denmark
Astellas Pharma Inc Leiden The Netherlands
Astellas Pharma Inc Northbrook Illinois
AZ Groeninge Kortrijk Kortrijk Belgium
Cliniques universitaires Saint Luc Brussels Belgium
Cologne University Cologne Germany
Herlev Hospital Herlev Denmark
Massachusetts General Hospital Cancer Center Boston Massachusetts
Medivation Inc San Francisco California
Rigshospitalet University of Copenhagen Copenhagen Denmark
Universitair ziekenhuis Brussels Brussels Belgium
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