A Phase III Comparison Between Concurrent Chemotherapy Plus Radiotherapy and Concurrent Chemotherapy Plus Radiotherapy Followed by Surgical Resection for Stage IIIA (N2) Non-Small Cell Lung Cancer
cisplatin
+ etoposide
+ conventional surgery
Adénocarcinome+13
+ Néoplasmes bronchiques
+ Carcinome
Étude thérapeutique
Résumé
Date de début de l'étude : 1 mars 1994
Date à laquelle le premier participant a commencé l'étude.OBJECTIVES: Primary Compare the progression-free survival, median (2-year) survival, and long-term (5-year) survival in patients with newly diagnosed, stage IIIA (N2) non-small cell lung cancer treated with radiotherapy concurrently with cisplatin and etoposide with or without surgical resection. Secondary Compare the patterns of local and distant failure in patients treated with these regimens. Determine the relationship of tobacco use, alcohol use, and diet with toxicity of these regimens and outcome in both men and women. OUTLINE: This is a randomized, multicenter study. Patients are stratified by contralateral mediastinal sampling or biopsy (yes vs no), tumor stage (T1 vs T2 vs T3), and performance status (70-80% vs 90-100%). Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive induction with cisplatin IV over 1 hour on days 1 and 8 and etoposide IV over 1 hour on days 1-5. Treatment continues every 4 weeks for 2 courses in the absence of disease progression or unacceptable toxicity. Beginning within 24 hours of the first dose of chemotherapy, patients undergo induction radiotherapy 5 days a week for 5 weeks in the absence of disease progression or unacceptable toxicity. Patients without local progression or distant metastases at 2-4 weeks after completion of course 2 undergo resection approximately 3-5 weeks after completion of course 2. All visible, accessible bronchopulmonary, hilar, and mediastinal lymph nodes are excised. The choice of surgical procedure (thoracotomy, lobectomy, or pneumonectomy with en bloc resection of tumor extending into the parietal pleura, chest wall, pericardium, or diaphragm) is at the discretion of the surgeon. Patients who undergo resection receive 2 additional courses of chemotherapy alone beginning 4-6 weeks postoperatively. Patients with unresectable disease or who are medically unfit for or refuse resection receive 2 additional courses of chemotherapy alone beginning immediately after completion of course 2. Arm II: Patients undergo induction chemoradiotherapy as in arm I but do not undergo resection. Patients without local progression or distant metastases within 1 week before anticipated completion of induction radiotherapy receive 2 additional courses of chemotherapy beginning immediately after completion of course 2. Patients without local or distant progression after completion of course 4 undergo boost radiotherapy for 8 days. Patients are followed every 2 months for 1 year, every 3 months for 2 years, and then every 6 months thereafter. PROJECTED ACCRUAL: A total of 510 patients will be accrued for this study within 4.9 years.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.429 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 18 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
DISEASE CHARACTERISTICS: Histologically or cytologically proven newly diagnosed, stage IIIA (T1-3, N2) non-small cell lung cancer Eligible subtypes: Adenocarcinoma Large cell carcinoma Squamous cell carcinoma Nonlobar and nondiffuse bronchoalveolar cell carcinoma Measurable or evaluable disease on chest x-ray and/or contrast CT scan Contrast thoracic CT required to complete staging Single primary bronchogenic tumor (no more than 1 parenchymal lung lesion) Pleural effusions allowed if 1 of the following conditions is met: Negative cytology on thoracentesis if effusions present before mediastinoscopy or exploratory thoracotomy Effusion seen on CT scan but not on chest x-ray and deemed too small to tap under CT or ultrasound guidance Positive ipsilateral mediastinal node(s) with or without positive ipsilateral hilar nodes Mediastinal nodes separate from primary lesion on CT scan or surgical exploration Histologic or cytologic proof of N2 disease by thoracotomy, mediastinoscopy, mediastinotomy, Chamberlain procedure, Wang needle, or fine needle aspiration under bronchoscopic or CT guidance Nodal biopsy or aspiration waived if all of the following conditions are met: Paralyzed left true vocal cord documented by bronchoscopy or indirect laryngoscopy Nodes visible in Level 5 region on CT scan Distinct primary lesion separate from nodes on CT scan All mediastinal nodal involvement mapped (positive or negative) No positive nodes in contralateral mediastinum (supraclavicular areas and higher) and neck Mediastinoscopy, mediastinotomy, Chamberlain procedure, or thoracotomy required for nodes larger than 1 cm on contrast CT scan Surgery waived if nodes negative or no larger than 1 cm on CT scan Lymphadenopathy allowed if biopsy proof of a benign cause No metastases by contrast CT or MRI scan of the brain, bone scan, CT scan of the lungs to exclude other ipsilateral or contralateral parenchymal lesions, and contrast CT scan of the upper abdomen including entire liver and adrenals No hepatomegaly or splenomegaly by physical examination or CT scan unless documentation of a benign cause No pericardial effusion No superior vena cava syndrome No prior diagnosis of lung cancer PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Karnofsky 90-100% (70-80% allowed if albumin at least 0.85 times lower limit of normal and weight loss no greater than 10% within 3 months before diagnosis) Hematopoietic: White blood cell count (WBC) at least 4,000/mm^3 OR Granulocyte count at least 2,000/mm^3 Platelet count normal Hemoglobin at least 10.0 g/dL (less than 8.5 g/dL allowed if no marrow involvement with tumor) Hepatic: See Performance status Bilirubin no greater than 1.5 times upper limit of normal (ULN)* Serum glutamate oxaloacetate transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT) no greater than 1.5 times ULN* NOTE: * Unless documentation of a benign cause Renal: Creatinine clearance at least 50 mL/min Cardiovascular: No myocardial infarction within the past 3 months No active angina No unstable arrhythmia No congestive heart failure Pulmonary: Forced expiratory volume at one second (FEV1) at least 2.0 liters OR Predicted postresection FEV1 at least 800 mL based on quantitative V/Q scan Diffusion capacity of lung for carbon monoxide (DLCO) at least 50% predicted (corrected for hemoglobin) if pneumonectomy planned or likely after induction chemotherapy Other: No clinically significant hearing loss unless willing to accept the potential of further loss No symptomatic peripheral neuropathy No peptic ulcer disease under active treatment No other medical illness not controllable by appropriate medical therapy No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or ductal or lobular carcinoma in situ of the breast Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: No concurrent colony-stimulating factors Chemotherapy: No prior chemotherapy for lung cancer No concurrent chemotherapy for another condition (such as arthritis) Endocrine therapy: Not specified Radiotherapy: No prior radiotherapy for lung cancer Surgery: See Disease Characteristics No prior resection of primary tumor
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.2 groupes d'intervention sont désignés dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalGroupe II
Comparateur actifObjectifs de l'étude
Objectifs principaux
Objectifs secondaires
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 16 sites
Indiana University Cancer Center
Indianapolis, United StatesVeterans Affairs Medical Center - Indianapolis (Roudebush)
Indianapolis, United StatesCCOP - Cedar Rapids Oncology Project
Cedar Rapids, United States