Phase II Study of Weekly Paclitaxel and Bryostatin-1 in Hormone Refractory Prostate Cancer
bryostatin 1
+ paclitaxel
Maladies génito-urinaires+7
+ Maladies Génitales
+ Maladies génitales masculines
Étude thérapeutique
Résumé
Date de début de l'étude : 1 mai 2000
Date à laquelle le premier participant a commencé l'étude.OBJECTIVES: I. Determine the onset, duration, and degree of response in patients with hormone-refractory, metastatic adenocarcinoma of the prostate treated with paclitaxel and bryostatin 1. II. Determine the toxicity of this regimen in these patients. III. Determine the overall survival of patients treated with this regimen. OUTLINE: This is an open-label, multicenter study. Patients receive paclitaxel IV over 1 hour on days 1, 8, and 15 and bryostatin 1 IV over 1 hour on days 2, 9, and 16. Treatment repeats every 4 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed monthly for 6 months and then every 3 months thereafter.
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.46 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.Homme
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 metastatic adenocarcinoma of the prostate that failed first- or second-line hormonal therapy (e.g., gonadal androgen suppression [orchiectomy or luteinizing hormone-releasing hormone] with or without antiandrogens) Failure on hormonal therapy is defined by 1 of the following criteria: Biochemical progression (after withdrawal of antiandrogens), documented by 3 rising PSA values, each value measured at least 2 weeks apart, with the last measurement being at least 25% of the nadir achieved while on hormonal therapy and with an increase in the absolute value by at least 5 ng/mL Measurable disease progression, defined by an increase in the sum of the products of the perpendicular diameters of any measurable lesion(s) by at least 25% Bone only progression allowed only with concurrent biochemical progression Castrate levels of testosterone (no greater than 50 ng/dL) No clinical signs/symptoms suggesting CNS metastases PATIENT CHARACTERISTICS: Age 18 and over Performance status ECOG 0-1 Life expectancy More than 6 months Hematopoietic WBC at least 3,000/mm^3 Absolute granulocyte count at least 1,500/mm^3 Platelet count at least 100,000/mm^3 Hepatic Bilirubin no greater than 1.5 times upper limit of normal (ULN) AST/ALT no greater than 2.5 times ULN Renal Creatinine no greater than 1.5 times ULN Calcium no greater than ULN Cardiovascular No uncontrolled or severe cardiovascular disease No myocardial infarction within the past 6 months No congestive heart failure No angina pectoris No active thromboembolic events within the past 3 months (e.g., deep venous thrombosis or cerebrovascular accident) Other No other serious medical or psychiatric illness No active infection No dementia or significantly altered mental status No prior or concurrent grade 1 or greater peripheral neuropathy No other prior or concurrent malignancy within the past 5 years except curatively treated nonmelanoma skin cancer HIV negative Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Chemotherapy No prior chemotherapy (including paclitaxel) Endocrine therapy At least 4 weeks since prior steroids or megestrol Radiotherapy At least 4 weeks since prior radiotherapy to bone lesions Other No other concurrent investigational therapy
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Un seul groupe d'intervention est désigné dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalCentres 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 4 sites
Greater Baltimore Medical Center and Cancer Center
Baltimore, United StatesOuvrir Greater Baltimore Medical Center and Cancer Center dans Google MapsComprehensive Cancer Center at Wake Forest University
Winston-Salem, United StatesFox Chase Cancer Center
Philadelphia, United StatesWellspan Health - York Cancer Center
York, United States