File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Docetaxel chemotherapy for Chinese patients with castrate-resistant prostate cancer

TitleDocetaxel chemotherapy for Chinese patients with castrate-resistant prostate cancer
Authors
KeywordsProstate neoplasms
Drug therapy
Androgen antagonists
Survival
Issue Date2013
Citation
Hong Kong Medical Journal, 2013, v. 19, n. 3, p. 237-241 How to Cite?
AbstractObjective To determine the effectiveness and toxicity of docetaxel for Chinese patients with castrate-resistant prostate cancer in a local Hong Kong hospital. Design Case series. Setting A tertiary cancer centre in Hong Kong. Patients In all, 39 castrate-resistant prostate cancer patients were treated with 3-weekly docetaxel at 75 mg/m 2 and prednisolone 10 mg daily between January 2006 and December 2011 in Queen Elizabeth Hospital. Main outcome measures Prostate-specific antigen control rate, pain control rate, progression-free survival, overall survival, and complication rates. Results The prostate-specific antigen response rate was 36%, and 27 (69%) of the patients had improved pain control after chemotherapy. The median progression-free survival, cancer-specific survival, and overall survival was 7.8 (95% confidence interval, 4.9-10.8) months, 13.0 (95% confidence interval, 9.6-16.3) months, and 12.2 (95% confidence interval, 9.3-15.1) months, respectively. The grade 3 anaemia and thrombocytopenia rates were 5%, and the neutropenic fever rate was 8%. Conclusions Chemotherapy with docetaxel at a dose of 75 mg/m 2 given once every 3 weeks together with daily prednisolone is well tolerated in Chinese and can offer good symptom palliation in suitable patients with castrate-resistant prostate cancer.
Persistent Identifierhttp://hdl.handle.net/10722/251623
ISSN
2023 Impact Factor: 3.1
2023 SCImago Journal Rankings: 0.261
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorCheun, F. Y.-
dc.contributor.authorLeung, K. C.-
dc.contributor.authorNgan, Roger K C-
dc.date.accessioned2018-03-08T05:00:30Z-
dc.date.available2018-03-08T05:00:30Z-
dc.date.issued2013-
dc.identifier.citationHong Kong Medical Journal, 2013, v. 19, n. 3, p. 237-241-
dc.identifier.issn1024-2708-
dc.identifier.urihttp://hdl.handle.net/10722/251623-
dc.description.abstractObjective To determine the effectiveness and toxicity of docetaxel for Chinese patients with castrate-resistant prostate cancer in a local Hong Kong hospital. Design Case series. Setting A tertiary cancer centre in Hong Kong. Patients In all, 39 castrate-resistant prostate cancer patients were treated with 3-weekly docetaxel at 75 mg/m 2 and prednisolone 10 mg daily between January 2006 and December 2011 in Queen Elizabeth Hospital. Main outcome measures Prostate-specific antigen control rate, pain control rate, progression-free survival, overall survival, and complication rates. Results The prostate-specific antigen response rate was 36%, and 27 (69%) of the patients had improved pain control after chemotherapy. The median progression-free survival, cancer-specific survival, and overall survival was 7.8 (95% confidence interval, 4.9-10.8) months, 13.0 (95% confidence interval, 9.6-16.3) months, and 12.2 (95% confidence interval, 9.3-15.1) months, respectively. The grade 3 anaemia and thrombocytopenia rates were 5%, and the neutropenic fever rate was 8%. Conclusions Chemotherapy with docetaxel at a dose of 75 mg/m 2 given once every 3 weeks together with daily prednisolone is well tolerated in Chinese and can offer good symptom palliation in suitable patients with castrate-resistant prostate cancer.-
dc.languageeng-
dc.relation.ispartofHong Kong Medical Journal-
dc.subjectProstate neoplasms-
dc.subjectDrug therapy-
dc.subjectAndrogen antagonists-
dc.subjectSurvival-
dc.titleDocetaxel chemotherapy for Chinese patients with castrate-resistant prostate cancer-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.12809/hkmj133804-
dc.identifier.pmid23568936-
dc.identifier.scopuseid_2-s2.0-84878864745-
dc.identifier.volume19-
dc.identifier.issue3-
dc.identifier.spage237-
dc.identifier.epage241-
dc.identifier.isiWOS:000320295600008-
dc.identifier.issnl1024-2708-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats