[HTML][HTML] Paclitaxel, 5-fluorouracil and hydroxyurea concurrent with radiation in locally advanced nasopharyngeal carcinoma

ASC Wong, RA Soo, JJ Lu, KS Loh, KS Tan… - Annals of …, 2006 - Elsevier
ASC Wong, RA Soo, JJ Lu, KS Loh, KS Tan, WS Hsieh, TP Shakespeare, ET Chua, HL Lim…
Annals of Oncology, 2006Elsevier
Background: Concurrent chemoradiotherapy (CRT) is the standard treatment for locally
advanced nasopharyngeal carcinoma (NPC). We conducted a phase II trial using paclitaxel,
5-fluorouracil and hydroxyurea concurrent with radiation (TFHX). Patients and methods: Fifty-
nine patients with locally advanced NPC were treated with CRT consisting of 4-day
continuous infusions of paclitaxel (20 mg/m 2/d) and 5-fluorouracil (600 mg/m 2/d), and oral
hydroxyurea 500 mg bid for nine doses, every 3 weeks concurrent with radiotherapy (RT) …
Abstract
Background: Concurrent chemoradiotherapy (CRT) is the standard treatment for locally advanced nasopharyngeal carcinoma (NPC). We conducted a phase II trial using paclitaxel, 5-fluorouracil and hydroxyurea concurrent with radiation (TFHX).
Patients and methods: Fifty-nine patients with locally advanced NPC were treated with CRT consisting of 4-day continuous infusions of paclitaxel (20 mg/m2/d) and 5-fluorouracil (600 mg/m2/d), and oral hydroxyurea 500 mg bid for nine doses, every 3 weeks concurrent with radiotherapy (RT). RT consisted of once daily 200cGy fractions 5 times per week to a total of 7000cGy.
Results: Complete response was seen in 86% and 71% of patients at 4 and 12 months after CRT. The median follow-up was 34 months. Twenty-three patients experienced relapse. Sixteen deaths occurred: 13 from progressive disease. Three-year overall survival and progression-free survival were 72% and 54% respectively, with locoregional and distant control rates of 83% and 64% at 3 years respectively. Grade 3 to 4 acute toxicities included oropharyngeal mucositis in 81% of patients treated, dermatitis in 63%, weight loss in 32%, and neutropenia in 22%. Neutropenic fever was seen in 14%. There were no treatment-related deaths from acute toxicity.
Conclusions: TFHX is shown to be feasible in NPC. Non-cross resistant induction chemotherapy should be further studied with this regimen.
Elsevier
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