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Is the Neoadjuvant Docetaxel, Cisplatin and 5-Fluorouracil Regimen Superior to Classic Cisplatin and 5-Fluorouracil for Locoregionally Advanced Nasopharyngeal Carcinoma?

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 Objectives: We retrospectively compared the toxicity and efficacy of two neoadjuvant chemotherapy regimens (docetaxel+cisplatin+5-fluorouracil vs. cisplatin+5-fluorouracil) followed by chemoradiotherapy for locoregionally advanced nasopharyngeal carcinoma. Patients and Materials: We analysed 135 patients with stage III and IVA-B nasopharyngeal carcinoma. Forty-four patients were treated with docetaxel+cisplatin+5-fluorouracil and chemoradiotherapy (TPF group), and 91 were treated with cisplatin+5-fluorouracil and chemoradiotherapy (PF group). Chemoradiotherapy was administered with weekly cisplatin. Radical radiotherapy with total doses of 70-74Gy was administered using a conventional technique, over 7 weeks in 2.0Gy/fraction; boost doses of 6-10Gy were administered in 55.6% patients (n=75) with locally advanced cancer. Results: The median follow-up was 46.5 months (range, 9.8-62.8 months), and the follow-up rate was 95%. The TPF group had better 5-year estimated progression-free survival (77.0% vs. 73.5%; P = 0.510) and overall survival than the PF group (80.7% vs. 77.9%, P = 0.446); however, there was no statistically significant difference between the groups. Toxicities in the two groups were similar; grade 3/4 oral mucositis was more common in the TPF group (27.3%) than in the PF group (15.3%) during chemoradiotherapy. Conclusions: The neoadjuvant docetaxel+cisplatin+5-fluorouracil chemotherapy led to satisfactory long-term survival and slight improvement in progression-free survival and overall survival as compared with the classic cisplatin+5-fluorouracil regimen; toxicity was tolerable. However, prospective trials are needed to prove whether docetaxel+cisplatin+5-fluorouracil is a substitute for cisplatin+5-fluorouracil.
Title: Is the Neoadjuvant Docetaxel, Cisplatin and 5-Fluorouracil Regimen Superior to Classic Cisplatin and 5-Fluorouracil for Locoregionally Advanced Nasopharyngeal Carcinoma?
Description:
 Objectives: We retrospectively compared the toxicity and efficacy of two neoadjuvant chemotherapy regimens (docetaxel+cisplatin+5-fluorouracil vs.
cisplatin+5-fluorouracil) followed by chemoradiotherapy for locoregionally advanced nasopharyngeal carcinoma.
Patients and Materials: We analysed 135 patients with stage III and IVA-B nasopharyngeal carcinoma.
Forty-four patients were treated with docetaxel+cisplatin+5-fluorouracil and chemoradiotherapy (TPF group), and 91 were treated with cisplatin+5-fluorouracil and chemoradiotherapy (PF group).
Chemoradiotherapy was administered with weekly cisplatin.
Radical radiotherapy with total doses of 70-74Gy was administered using a conventional technique, over 7 weeks in 2.
0Gy/fraction; boost doses of 6-10Gy were administered in 55.
6% patients (n=75) with locally advanced cancer.
Results: The median follow-up was 46.
5 months (range, 9.
8-62.
8 months), and the follow-up rate was 95%.
The TPF group had better 5-year estimated progression-free survival (77.
0% vs.
73.
5%; P = 0.
510) and overall survival than the PF group (80.
7% vs.
77.
9%, P = 0.
446); however, there was no statistically significant difference between the groups.
Toxicities in the two groups were similar; grade 3/4 oral mucositis was more common in the TPF group (27.
3%) than in the PF group (15.
3%) during chemoradiotherapy.
Conclusions: The neoadjuvant docetaxel+cisplatin+5-fluorouracil chemotherapy led to satisfactory long-term survival and slight improvement in progression-free survival and overall survival as compared with the classic cisplatin+5-fluorouracil regimen; toxicity was tolerable.
However, prospective trials are needed to prove whether docetaxel+cisplatin+5-fluorouracil is a substitute for cisplatin+5-fluorouracil.

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