A Prospective Randomised Trial Comparing Temozolomide With PCV In The Treatment Of Recurrent WHO Astrocytic Tumours Grades III And IV
Collecte de données
Astrocytome+15
+ Maladies du cerveau
+ Néoplasmes cérébraux
Étude thérapeutique
Résumé
Date de début de l'étude : 1 octobre 2002
Date à laquelle le premier participant a commencé l'étude.OBJECTIVES: * Compare the efficacy of temozolomide vs procarbazine, lomustine, and vincristine, in terms of overall survival, in patients with recurrent malignant glioma. * Compare progression-free survival of patients treated with these regimens. * Compare progression-free survival at 12 weeks in patients treated with two different schedules of temozolomide. * Compare the overall survival of patients treated with two different schedules of temozolomide. * Compare toxic effects of two different schedules of temozolomide in these patients. * Compare quality of life of patients treated with these regimens. OUTLINE: This is a randomized, controlled, open-label, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I:Patients are randomized to 1 of 2 treatment schedules: * Schedule 1: Patients receive oral temozolomide once daily on days 1-5. * Schedule 2:Patients receive oral temozolomide once daily on days 1-21. Treatment on both schedules repeats every 4 weeks for a maximum of 9 courses in the absence of disease progression or unacceptable toxicity. * Arm II:Patients receive oral lomustine and vincristine IV on day 1 and oral procarbazine on days 1-21. Treatment repeats every 6 weeks for a maximum of 6 courses in the absence of disease progression or unacceptable toxicity. Quality of life is assessed at baseline and at 12 and 24 weeks. Patients are followed every 12 weeks. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 500 patients (250 per treatment arm) will be accrued for this study.
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.500 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 confirmed anaplastic astrocytoma, glioblastoma multiforme, or gliosarcoma * WHO grade III or IV at diagnosis or relapse * Must have undergone primary therapy including radiotherapy * Must be in first recurrence confirmed by CT scan or MRI * Evaluable disease by CT scan or MRI PATIENT CHARACTERISTICS: Age * 18 and over Performance status * WHO 0-3 Life expectancy * At least 1 month Hematopoietic * Absolute neutrophil count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic * Total and direct bilirubin less than 1.5 times upper limit of normal (ULN) * SGOT or SGPT less than 3 times ULN * Alkaline phosphatase less than 2 times ULN Renal * BUN less than 1.5 times ULN * Creatinine less than 1.5 times ULN Other * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * No other concurrent serious illness * Considered fit to receive chemotherapy PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * No prior chemotherapy for glioma Endocrine therapy * Not specified Radiotherapy * See Disease Characteristics * At least 2 months since prior radiotherapy * No prior radiosurgery, interstitial radiotherapy, or brachytherapy for glioma Surgery * Prior debulking surgery for recurrent disease allowed
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Objectifs 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 1 site
Medical Research Council Clinical Trials Unit
London, United KingdomOuvrir Medical Research Council Clinical Trials Unit dans Google Maps