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Please use this identifier to cite or link to this item: https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/233
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dc.contributor.authorWong, A. S.-
dc.contributor.authorSoo, R. A.-
dc.contributor.authorLu, J. J.-
dc.contributor.authorLoh, K. S.-
dc.contributor.authorTan, K. S.-
dc.contributor.authorHsieh, W. S.-
dc.contributor.authorShakespeare, T. P.-
dc.contributor.authorChua, E. T.-
dc.contributor.authorLim, H. L.-
dc.contributor.authorGoh, B. C.-
dc.date.accessioned2024-12-04T04:50:37Z-
dc.date.available2024-12-04T04:50:37Z-
dc.date.issued2006-07-
dc.identifier.citationAnnals of Oncology. 2006 Jul;17(7):1152-7. doi: 10.1093/annonc/mdl090.en
dc.identifier.urihttps://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/233-
dc.description.abstractBackground: 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). 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.en
dc.language.isoenen
dc.subjectHydroxyureaen
dc.subjectFluorouracilen
dc.subjectPaclitaxelen
dc.subjectNasopharyneal Carcinomaen
dc.subjectChemoradiotherapyen
dc.subjectProgression-Free Survivalen
dc.subjectMucositisen
dc.subjectDermatitisen
dc.titlePaclitaxel, 5-fluorouracil and hydroxyurea concurrent with radiation in locally advanced nasopharyngeal carcinomaen
dc.typeArticleen
dc.contributor.mnclhdauthorShakespeare, Thomas P.-
Appears in Collections:Oncology / Cancer

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