Castration-Resistant Prostate Cancer

التفاصيل البيبلوغرافية
العنوان: Castration-Resistant Prostate Cancer
المؤلفون: Riccardo Autorino, Cora N. Sternberg, Carlo Buonerba, Sabino De Placido, Giuseppe Di Lorenzo
المساهمون: Di Lorenzo, G., Buonerba, Carlo, Autorino, Riccardo, DE PLACIDO, Sabino, Strernberg, C. N., Di Lorenzo, G, Buonerba, C, De Placido, S, Sternberg, Cn
المصدر: Drugs. 70:983-1000
بيانات النشر: Springer Science and Business Media LLC, 2010.
سنة النشر: 2010
مصطلحات موضوعية: Endothelin Receptor Antagonists, Male, Oncology, medicine.medical_specialty, Bevacizumab, Angiogenesis Inhibitors, Antineoplastic Agents, Satraplatin, Cancer Vaccines, Prostate cancer, chemistry.chemical_compound, Internal medicine, medicine, Humans, Pharmacology (medical), Aflibercept, Clinical Trials as Topic, business.industry, RANK Ligand, Prostatic Neoplasms, Cancer, Androgen Antagonists, Protein-Tyrosine Kinases, medicine.disease, Clinical trial, Clusterin, Docetaxel, chemistry, Cabazitaxel, Immunology, business, Orchiectomy, medicine.drug
الوصف: Until very recently, docetaxel was the only approved agent in castration-resistant prostate cancer (CRPC) and other effective therapeutic options are urgently needed. In recent years, several new agents with promising activity and a favourable toxicity profile have been developed and clinically investigated in the fields of hormonal, cytotoxic, targeted and immune therapy. In particular, recent results from two large phase III trials of sipuleucel-T and cabazitaxel show that these two agents significantly prolong overall survival in CRPC. Indeed, sipuleucel-T has recently been approved by the US FDA for the treatment of CRPC. Many other pharmaceuticals, which are presented in this review, have been investigated recently or are being investigated in phase III trials and might prove to be effective in the future. Reviewed articles are discussed in light of the innovations in study design brought by the Prostate Cancer Clinical Trials Working Group (PCWG2), which updated the Prostate-Specific Antigen Working Group (PCWG1) guidelines, in order to allow better identification of potentially active drugs in clinical trials.
وصف الملف: STAMPA
تدمد: 0012-6667
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b55b667b1df4188d4681333a534d6c53Test
https://doi.org/10.2165/10898600-000000000-00000Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....b55b667b1df4188d4681333a534d6c53
قاعدة البيانات: OpenAIRE