» Articles » PMID: 17960013

Cisplatin and Fluorouracil Alone or with Docetaxel in Head and Neck Cancer

Abstract

Background: A randomized phase 3 trial of the treatment of squamous-cell carcinoma of the head and neck compared induction chemotherapy with docetaxel plus cisplatin and fluorouracil (TPF) with cisplatin and fluorouracil (PF), followed by chemoradiotherapy.

Methods: We randomly assigned 501 patients (all of whom had stage III or IV disease with no distant metastases and tumors considered to be unresectable or were candidates for organ preservation) to receive either TPF or PF induction chemotherapy, followed by chemoradiotherapy with weekly carboplatin therapy and radiotherapy for 5 days per week. The primary end point was overall survival.

Results: With a minimum of 2 years of follow-up (> or =3 years for 69% of patients), significantly more patients survived in the TPF group than in the PF group (hazard ratio for death, 0.70; P=0.006). Estimates of overall survival at 3 years were 62% in the TPF group and 48% in the PF group; the median overall survival was 71 months and 30 months, respectively (P=0.006). There was better locoregional control in the TPF group than in the PF group (P=0.04), but the incidence of distant metastases in the two groups did not differ significantly (P=0.14). Rates of neutropenia and febrile neutropenia were higher in the TPF group; chemotherapy was more frequently delayed because of hematologic adverse events in the PF group.

Conclusions: Patients with squamous-cell carcinoma of the head and neck who received docetaxel plus cisplatin and fluorouracil induction chemotherapy plus chemoradiotherapy had a significantly longer survival than did patients who received cisplatin and fluorouracil induction chemotherapy plus chemoradiotherapy. (ClinicalTrials.gov number, NCT00273546 [ClinicalTrials.gov].).

Citing Articles

Efficacy and safety of nanoparticle albumin-bound paclitaxel plus cisplatin or nedaplatin plus tegafur/gimeracil/oteracil as induction chemotherapy regimen for hypopharyngeal cancer.

Jiang C, Liu Y, Mo Y, Xu L, Zhu L, Li Z Front Oncol. 2025; 15:1504658.

PMID: 40066095 PMC: 11891220. DOI: 10.3389/fonc.2025.1504658.


Phase II clinical trial assessing the addition of hyperthermia to salvage concurrent chemoradiotherapy for unresectable recurrent head and neck cancer in previously irradiated patients.

Yang K, Chi M, Hao C, Ko H, Huang Y, Wu R Radiat Oncol. 2025; 20(1):21.

PMID: 39920700 PMC: 11806545. DOI: 10.1186/s13014-025-02585-z.


Superior 125-month outcome through cetuximab in the larynx organ preservation trial DeLOS-II: a single study center's experience.

Wichmann G, Wald T, Zebralla V, Stoehr M, Pirlich M, Wiegand S Front Oncol. 2025; 14():1506840.

PMID: 39777347 PMC: 11703891. DOI: 10.3389/fonc.2024.1506840.


Random survival forest predicts survival in patients with metastatic laryngeal and hypopharyngeal cancer and the prognostic benefits of surgery and radiotherapy.

Wang Y, Li C, Yang F, Gong M, Qu J, Ma R J Cancer. 2025; 16(2):603-621.

PMID: 39744488 PMC: 11685675. DOI: 10.7150/jca.103793.


Dendritic cell effector mechanisms and tumor immune microenvironment infiltration define TLR8 modulation and PD-1 blockade.

Ruiz-Torres D, Wise J, Zhao B, Oliveira-Costa J, Cavallaro S, Sadow P Front Immunol. 2024; 15():1440530.

PMID: 39697344 PMC: 11652363. DOI: 10.3389/fimmu.2024.1440530.