Low-Dose Docetaxel Combined with Dexamethasone Is Feasible for Patients with Castration-Resistant Prostate Cancer
Autor: | Masayoshi Yokoyama, Kenichi Nishimura, Noriyoshi Miura, Yuki Miyauchi, Nozomu Tanji, Akitomi Shirato, Seiji Asai, Yutaka Yanagihara, Terutaka Noda, Tadahiko Kikugawa |
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Rok vydání: | 2015 |
Předmět: |
Male
0301 basic medicine Oncology medicine.medical_specialty medicine.medical_treatment Docetaxel urologic and male genital diseases Gastroenterology Dexamethasone 03 medical and health sciences Prostate cancer 0302 clinical medicine Internal medicine Antineoplastic Combined Chemotherapy Protocols Drug Discovery medicine Humans Pharmacology (medical) Survival rate Aged Neoplasm Staging Retrospective Studies Aged 80 and over Pharmacology Chemotherapy Dose-Response Relationship Drug business.industry Retrospective cohort study General Medicine Middle Aged Prognosis medicine.disease Survival Rate Prostatic Neoplasms Castration-Resistant 030104 developmental biology Infectious Diseases 030220 oncology & carcinogenesis Toxicity Feasibility Studies Taxoids business Febrile neutropenia Follow-Up Studies medicine.drug |
Zdroj: | Chemotherapy. 61:23-31 |
ISSN: | 1421-9794 0009-3157 |
Popis: | Aim: Docetaxel-based chemotherapy against castration-resistant prostate cancer (CRPC) has recently been shown to be effective and tolerable. The objective of this study was to retrospectively evaluate the efficacy and toxicity of low-dose docetaxel in combination with dexamethasone. Methods: Thirty-seven CRPC patients were administered a treatment regimen consisting of 50 mg/m2 docetaxel once every 3-4 weeks and 1 mg dexamethasone daily at our institution, between November 2004 and April 2014. Results: Twenty-four patients (65%) had a decrease in serum prostate-specific antigen (PSA) >50%. The median overall survival (OS) and PSA progression-free survival were 26.2 and 10.0 months, respectively. Ten of 12 patients (83%) taking analgesic agents reduced their intake because of decreased pain levels. Grade 3 febrile neutropenia occurred in 2 patients (5%). Nonhematological toxicities were less frequent but sometimes severe. Treatment-related death occurred in 2 octogenarian patients, 1 due to gastric bleeding and the other due to infective endocarditis. Conclusion: Low-dose docetaxel in combination with dexamethasone is feasible in Japanese CRPC patients. Hematological toxicity is less than that seen with standard docetaxel therapy, but it is necessary to monitor patients for severe nonhematological toxicities, particularly very elderly patients. |
Databáze: | OpenAIRE |
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