Phase II Study of Weekly Paclitaxel and Bryostatin-1 in Hormone Refractory Prostate Cancer
bryostatin 1
+ paclitaxel
Enfermedades Urogenitales+6
+ Enfermedades Genitales
+ Enfermedades Genitales Masculinas
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de mayo de 2000
Fecha en la que se inscribió al primer participante.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.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 46 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Hombre
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
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 Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Un solo grupo de intervención está designado en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalCentros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene 4 ubicaciones
Greater Baltimore Medical Center and Cancer Center
Baltimore, United StatesAbrir Greater Baltimore Medical Center and Cancer Center en 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