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Preliminary result of multi-center clinical trial on the docetaxel, 5-Fu and DDP in the treatment of advanced, recurrent or metastatic nasopharyngeal carcinoma / 中华肿瘤杂志
Zhonghua zhong liu za zhi ; (12): 314-316, 2008.
Article in Zh | WPRIM | ID: wpr-348104
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>This clinical study was designed to evaluate the efficacy and toxicity of the combined regimen of docetaxel, 5-Fu and DDP (TPF) in the treatment of advanced or relapsed nasopharyngeal carcinoma (NPC).</p><p><b>METHODS</b>Fifty-six patients with newly diagnosed or recurrent/metastatic NPC following chemotherapy or radiotherapy were enrolled. Both docetaxel and DDP were administered intravenously for 6 hours at the dose of 70 mg/m2 on D1. 5-Fu was given at a dose of 400-500 mg/m2 for 6 hours from D1 to D5. Dexamethasone was routinely administered before injection of docetaxel. This combination was repeated every 3 to 4 weeks, and continued for 4-6 cycles or until PD for the responders.</p><p><b>RESULTS</b>Fifty-one (91.1%) patients were evaluable for response assessment. The response rate for whole group was 72.5% (37/51) with a CR rate of 9.8% (5/51). The stable disease accounted for 17.6% (9/51). There were 17(30.4%) chemotherapy-naïve patients. The overall response rate in those was 82.4% with a CR rate of 29.4%. However, the response rate for previously treated patients was 64.7% without CR. Twelve patients had progressed disease, including 5 (8.9%) died of disease progression with a median follow-up of 11 month (ranged from 1 to 19 months). Totally, 196 courses of chemotherapy were administered. The major toxicity was myelosupression, nausea/vomiting. The incidence of leucopenia was 48% with 22.2% of these in NCI grade II or IV. But only 2 patients (3.6%) experienced leucopenia with a fever. Other mild toxicities including alopecia, asthenia, mucositis and diarrhea were also observed.</p><p><b>CONCLUSION</b>Our preliminary outcome shows docetaxel, 5-Fu and DDP combination is effective and safe for the patients with advanced or relapsed nasopharyngeal carcinoma. But further clinical study is warranted.</p>
Subject(s)
Full text: 1 Index: WPRIM Main subject: Pathology / Remission Induction / Carcinoma, Squamous Cell / Antineoplastic Combined Chemotherapy Protocols / Nasopharyngeal Neoplasms / Follow-Up Studies / Cisplatin / Taxoids / Therapeutic Uses / Drug Therapy Type of study: Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male Language: Zh Journal: Zhonghua zhong liu za zhi Year: 2008 Type: Article
Full text: 1 Index: WPRIM Main subject: Pathology / Remission Induction / Carcinoma, Squamous Cell / Antineoplastic Combined Chemotherapy Protocols / Nasopharyngeal Neoplasms / Follow-Up Studies / Cisplatin / Taxoids / Therapeutic Uses / Drug Therapy Type of study: Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male Language: Zh Journal: Zhonghua zhong liu za zhi Year: 2008 Type: Article