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Reduced Radiotherapy With Pac/Cis vs Standard Radiotherapy With 5-FU/Cis in Locally Advanced Head and Neck Cancer

Phase 3
Terminated
Conditions
Head and Neck Cancer
Interventions
Drug: 5-FU/Cisplatin
Radiation: Reduced RT
Radiation: Standard RT
Registration Number
NCT01126216
Lead Sponsor
University of Erlangen-Nürnberg Medical School
Brief Summary

Reduced RT with Pac/Cis vs. standard RCT with 5-FU/Cis

Detailed Description

Standard treatment for patients with advanced, unresectable head and neck cancer is a platin-based simultaneous radiochemotherapy (RCT) (Pignon JP et al., Lancet 2000;355:949-955). However, irradiation dose is still debatable regarding local tumor control and late toxicity. Moreover, it is still unclear which combination of different drugs might be more effective.

In recent years, new drugs have been introduced in the field of head and neck cancer. The Taxanes, namely Docetaxel and Paclitaxel, have been investigated in several phase I/II-studies, and showed promising results concerning locoregional control rates and survival data. The RTOG 97-03 trial (Garden et al., J Clin Oncol 2004; 22:2856-64) compared a RCT either with Cisplatin/5-FU or Cisplatin/Paclitaxel. In this phase II-study an improvement of local tumor control and disease free survival of 15-20% in favour of the Cisplatin/Paclitaxel treatment arm was seen.

Therefore, our phase III-trial compares a standard RCT (70.6 Gy) with Cisplatin/5-FU to a RCT with Cisplatin/Paclitaxel and reduced irradiation dose (63.6 Gy). Primary endpoint is to proof superiority of the experimental Cisplatin/Paclitaxel treatment arm concerning disease-free-survival. Secondary endpoints are locoregional tumor control, overall survival and quality of life.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
221
Inclusion Criteria
  • Histologically proven, locally advanced stage III-IV A-B (UICC 2002) primary squamous cell carcinoma of the oral cavity, the oropharynx, the hypopharynx, the supraglottic larynx
  • Age ≥ 18
  • Written informed consent for the participation in the clinical trial
Exclusion Criteria
  • Inadequate hepatic function: Bilirubin > 2,0 mg/dl, SGOT, SGPT, AP, Gamma-GT > 3 x ULN
  • Inadequate bone marrow function: leukocytes < 3,5 x 10^9/l, platelets < 100 x 10^9/l or neutrophils < 1,5 x 10^9/l
  • Serum creatinine > 1,5 mg/dl, creatinine clearance < 60ml/min
  • Uncontrolled severe somatic or psychological disease: e.g. unstable angina pectoris; myocardial infarction during the last 6 months; significant cardial rhythm disorders; apoplexy; high grade stenosis of the carotis; neurological or psychiatric disorders including convulsive disorders; dementia; psychosis; active uncontrolled infection or sepsis; liver cirrhosis; Child stage B,C; severe liver function disorders; marginal changes in the blood count; severe kidney damage; HIV-infection
  • Acute infections
  • Fertile women without adequate contraception during and up to 6 months after therapy (the method of contraception has to be high effective as described in the Note for guidance on non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals (CPMP/ICH/286/95 mod) and it has to be discussed with the investigator)
  • Pregnant or breast feeding women
  • Men, who are not willing to use adequate contraception during and up to 6 months after therapy, that is discussed with the investigator
  • ECOG-Status > 1
  • Reduced hearing function (especially higher frequencies)
  • Exsiccosis
  • Neuropathy, caused by cisplatin
  • Concurrent malignancies, with exception of adequately treated basal cell carcinoma of the skin or in situ carcinoma or the cervix
  • Prior radiotherapy of the neck or chemotherapy
  • Distant metastasis
  • Recurrent carcinoma in the head and neck region
  • Prior neck-dissection or surgical intervention exceeding an exploratory excision
  • Known intolerance to 5-Fluorouracil
  • Known deficit of Dihydropyrimidine dehydrogenase (DPD)
  • Simultaneous therapy with Brivudin or other inhibitors of DPD
  • Known intolerance to Cisplatin or other substances that contain platin
  • Known intolerance to Paclitaxel or one of the included substances, especially to Poly(oxyethylene)Rhizinusöl/Macrogolglycerol ricinoleate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Reduced RT + Pacitaxel/CisplatinPaclitaxel/Cisplatin63,6 Gy accelerated hyperfractionated radiotherapy with Paclitaxel (20mg/m\^2/d) on days 2, 5, 8, 11 and 25, 30, 33, 36) and Cisplatin (20mg/m\^2/d) on days 1-4 and 29-32, followed by a salvage operation or neck dissection if there is persisting tumor
Reduced RT + Pacitaxel/CisplatinReduced RT63,6 Gy accelerated hyperfractionated radiotherapy with Paclitaxel (20mg/m\^2/d) on days 2, 5, 8, 11 and 25, 30, 33, 36) and Cisplatin (20mg/m\^2/d) on days 1-4 and 29-32, followed by a salvage operation or neck dissection if there is persisting tumor
Standard RT + 5-Fluorouracil/Cisplatin5-FU/Cisplatin70,6 Gy accelerated hyperfractionated radiotherapy with 5-Fluorouracil(600mg/m\^2/d) on days 1-5 and 29-33) and Cisplatin (20mg/m\^2/d) on days 1-5 and 29-33, followed by a salvage operation or neck dissection if there is persisting tumor
Standard RT + 5-Fluorouracil/CisplatinStandard RT70,6 Gy accelerated hyperfractionated radiotherapy with 5-Fluorouracil(600mg/m\^2/d) on days 1-5 and 29-33) and Cisplatin (20mg/m\^2/d) on days 1-5 and 29-33, followed by a salvage operation or neck dissection if there is persisting tumor
Primary Outcome Measures
NameTimeMethod
Disease free survival3 years
Secondary Outcome Measures
NameTimeMethod
Overall Survival3 years
Distant metastasis free survival3 years
Local control3 years
Acute and Late Toxicity4 years
Life Quality4 years
HPV/p16-StatusEnd of study

Trial Locations

Locations (13)

Klinikum St. Elisabeth Straubing, Klinik für Hals-Nasen-Ohren-Heilkunde

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Straubing, Germany

Universitätsklinikum Erlangen, Strahlenklinik

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Erlangen, Germany

Kliniken Maria Hilf GmbH Mönchengladbach, Klinik für Strahlentherapie

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Mönchengladbach, Germany

Brüderkrankenhaus st. Josef Paderborn, Klinik für Strahlentherapie

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Paderborn, Germany

MVZ am Klinikum Mutterhaus der Borrmäerinnen, Strahlentherapie

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Trier, Germany

Klinikum München Pasing und Perlach, Klinik für HNO

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München, Germany

Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Klinik und Poliklinik für Hals-Nasen- und Ohrenkranke

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Lübeck, Germany

Universitätsklinikum Frankfurt, Klinik für Strahlentherapie und Radioonkologie

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Frankfurt/M., Germany

Klinikum Coburg, Strahlentherapie, DiaCura

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Coburg, Germany

Universitätsklinikum Düsseldorf, Klinik und Poliklinik für Strahlentherapie und Radiologische Onkologie

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Düsseldorf, Germany

Universitätsklinikum des Saarlandes, Klinik für Strahlentherapie und Radioonkologie,

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Homburg/Saar, Germany

Klinikum am Eichert, Praxis für Strahlentherapie und Klinik für Radioonkologie

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Göppingen, Germany

Universitätsklinikum Regensburg, Klinik und Poliklinik für Strahlentherapie

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Regensburg, Germany

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