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Cancer Invest ; 32(9): 445-50, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25259606

ABSTRACT

We present a single-institution experience reporting the efficacy and safety of docetaxel, administered as first-line chemotherapy, in castration-resistant prostate cancer (CRPC), focusing on patients and treatment parameters. From November 2004 to January 2012, 51 patients received chemotherapy with docetaxel. With a mean follow-up time (from the beginning of CHT) of 1.6 years (range 0.1-5.1 years), 35 patients (68.6%) died for prostate cancer and 48 patients (94.1%) showed progression of the disease. Five factors influenced overall survival: nodal status at diagnosis, neoadjuvant hormonal therapy, number of cycles of docetaxel administered, schedule of docetaxel and ECOG performance status before starting chemotherapy.


Subject(s)
Prostatic Neoplasms, Castration-Resistant/drug therapy , Taxoids/therapeutic use , Administration, Intravenous , Aged , Aged, 80 and over , Anemia/chemically induced , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/adverse effects , Antineoplastic Agents/therapeutic use , Docetaxel , Drug Administration Schedule , Fatigue/chemically induced , Humans , Kaplan-Meier Estimate , Leukopenia/chemically induced , Male , Middle Aged , Outcome Assessment, Health Care/statistics & numerical data , Proportional Hazards Models , Taxoids/administration & dosage , Taxoids/adverse effects
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