Resumen
Initial therapy for advanced prostate cancer includes androgen ablation by surgical or medical castration. Still, nearly all men with metastases will progress to hormone-refractory prostate cancer (HRPC). Current U.S. Food and Drug Administration-approved agents for the treatment of HRPC include mitoxantrone and estramustine, although the vinca alkaloids and the taxanes have shown promising activity in single-agent phase II trials. Combinations of these agents induce a biochemical response in greater than 50% of patients, but the median duration of response is approximately 6 months. Overall survival of patients treated with these combinations is approximately 18-24 months. Studies are ongoing to develop novel therapies that target specific molecular pathways or mechanisms of chemotherapy resistance. Novel agents under development include growth factor receptor inhibitors, anti-sense oligonucleotides, bisphosphonates, and cell differentiating agents. Evaluation and incorporation of these agents into existing treatment regimens will guide us in the development of more active regimens in the treatment of HRPC.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 360-370 |
| Número de páginas | 11 |
| Publicación | Oncologist |
| Volumen | 7 |
| N.º | 4 |
| DOI | |
| Estado | Published - 2002 |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- General Medicine
Huella
Profundice en los temas de investigación de 'State-of-the-art treatment of metastatic hormone-refractory prostate cancer'. En conjunto forman una huella única.Citar esto
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