The purpose of the present trial is to assess if induction concurrent chemoradiotherapy followed by consolidation chemotherapy will improve survival in comparison with the same chemotherapy given as induction followed by consolidation concurrent chemoradiotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
125
Concurrent chemoradiotherapy: Radiotherapy 66 Gy in 2 Gy/fraction, 5 fractions/wk (6.5 weeks)with Cisplatin 20 mg/m²/week (6 times, beginning on day 1 of radiotherapy)and Docetaxel 20 mg/m²/week (6 times, beginning on day 1 of radiotherapy) Chemotherapy : Cisplatin 60 mg/m² and Docetaxel 75 mg/m² on day 1
Concurrent chemoradiotherapy: Radiotherapy 66 Gy in 2 Gy/fraction, 5 fractions/wk (6.5 weeks)with Cisplatin 20 mg/m²/week (6 times, beginning on day 1 of radiotherapy)and Docetaxel 20 mg/m²/week (6 times, beginning on day 1 of radiotherapy) Chemotherapy : Cisplatin 60 mg/m² and Docetaxel 75 mg/m² on day 1
Department of Pneumology RHMS Hôpital de la Madeleine
Ath, Belgium
Department of Pneumology Clinique Saint-Luc
Bouge, Belgium
Survival
Time frame: Survival will be dated from the day of randomisation until death or last follow up
Response rate
Time frame: At the end of the whole treatment
Toxicity
Time frame: After each course of chemotherapy and at the end of treatment
Local control rate
Time frame: After completion of treatment
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Department of Pneumology CHR St Joseph-Warquignies
Boussu, Belgium
Department of Intensive Care Unit and Thoracic Oncology Institut Jules Bordet
Brussels, Belgium
Department of Pneumology Hospital Ixelles-Molière
Brussels, Belgium
Department of Pneumology CHU Charleroi
Charleroi, Belgium
Department of Pneumology Hôpital Saint-Joseph
Gilly, Belgium
Hôpital Ambroise Paré
Mons, Belgium
Hôpital Vésale - Montigny-le-Tilleul
Montigny-le-Tilleul, Belgium
Department of Pneumology Centre Hospitalier de Mouscron
Mouscron, Belgium
...and 9 more locations