Source:http://linkedlifedata.com/resource/pubmed/id/15762353
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2005-3-14
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pubmed:abstractText |
Prostate cancer represents one of the most important health problems in industrialized countries. It is the second leading cause of cancer-related death in the United States. Therapeutic options are different according to the stage of the disease at the diagnosis. Patients with localized disease may be treated with surgery or radiation, whereas the treatment for patients with a metastatic disease is purely palliative. Hormonal treatment represents the standard therapy for stage IV prostate cancer, but patients ultimately become unresponsive to androgen ablation and are classified as hormone-refractory prostate cancer patients. The molecular mechanisms involved in progression in hormone resistance are characterized by mutations, down and up-regulation in the androgen receptor gene, mutations in p53 and over-expression of Bcl2 and other alterations in genes and in gene expression. The important thing is that we understand these mechanisms to define potential therapeutic agents for the treatment of hormone-refractory prostate cancer patients. Conventional options for patients with hormone-refractory prostate cancer include secondary hormone therapy, radiotherapy and cytotoxic chemotherapy. The commonest antineoplastic agents are mitoxantrone, estramustine and taxanes. Despite an improvement in the palliative benefit, none of these agents has demonstrated a beneficial impact on the overall survival of patients. Therefore, there is no standard therapy for these patients, thus we need new approaches which should be studied in clinical trials. The evaluation and incorporation of new agents into current treatment regimens could have a role in the treatment of hormone-refractory prostate cancer, but their efficacy has not yet been demonstrated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Androgen Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, Hormonal,
http://linkedlifedata.com/resource/pubmed/chemical/Estramustine,
http://linkedlifedata.com/resource/pubmed/chemical/Mitoxantrone,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Androgen,
http://linkedlifedata.com/resource/pubmed/chemical/Taxoids
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pubmed:status |
MEDLINE
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pubmed:issn |
0300-8916
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pubmed:author |
pubmed-author:BajettaEmilioE,
pubmed-author:BianchiniGianpaoloG,
pubmed-author:Della TorreSilviaS,
pubmed-author:FerrariLeonardoL,
pubmed-author:FusiAlbertoA,
pubmed-author:MartinettiAntoniaA,
pubmed-author:ProcopioGiuseppeG,
pubmed-author:RicottaRiccardoR,
pubmed-author:SalvioniRobertoR,
pubmed-author:SavelliGiordanoG,
pubmed-author:VillaSergioS
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pubmed:issnType |
Print
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pubmed:volume |
90
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
535-46
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pubmed:dateRevised |
2008-12-12
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pubmed:meshHeading |
pubmed-meshheading:15762353-Androgen Antagonists,
pubmed-meshheading:15762353-Antineoplastic Agents, Hormonal,
pubmed-meshheading:15762353-Clinical Trials, Phase II as Topic,
pubmed-meshheading:15762353-Drug Resistance, Neoplasm,
pubmed-meshheading:15762353-Estramustine,
pubmed-meshheading:15762353-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:15762353-Humans,
pubmed-meshheading:15762353-Male,
pubmed-meshheading:15762353-Mitoxantrone,
pubmed-meshheading:15762353-Neoplasm Staging,
pubmed-meshheading:15762353-Palliative Care,
pubmed-meshheading:15762353-Prostatic Neoplasms,
pubmed-meshheading:15762353-Receptors, Androgen,
pubmed-meshheading:15762353-Survival Analysis,
pubmed-meshheading:15762353-Taxoids,
pubmed-meshheading:15762353-Treatment Outcome
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pubmed:articleTitle |
Treatment options in hormone-refractory metastatic prostate carcinoma.
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pubmed:affiliation |
Medical Oncology Unit B, National Institute for the Study and the Treatment of Tumors, Milan, Italy.
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pubmed:publicationType |
Journal Article,
Review
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