A Phase I Study of STI571 in Ph+ Leukemia
imatinib mesylate
+ imatinib mesylate
+ imatinib mesylate
Enfermedades de la Médula Ósea+14
+ Enfermedad Crónica
+ Enfermedades Hematológicas
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de enero de 2002
Fecha en la que se inscribió al primer participante.OBJECTIVES: Determine the maximum tolerated dose and dose-limiting toxicity of imatinib mesylate in patients with recurrent Philadelphia chromosome-positive leukemia. Characterize the pharmacokinetic behavior of this drug in this patient population. Determine preliminarily the antileukemic activity of this drug in these patients. OUTLINE: This is a dose-escalation, multicenter study. Patients receive oral imatinib mesylate (STI571) once daily for 28 days. Treatment continues in the absence of unacceptable toxicity or disease progression. Cohorts of 3-6 patients receive escalating doses of STI571 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which at least 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Patients are followed every 6 months for 4 years and then annually thereafter. PROJECTED ACCRUAL: A maximum of 32 patients will be accrued for this study within 3.5 years.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 31 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.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.Hasta 21 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: Recurrent Philadelphia (Ph) chromosome-positive leukemia Recurrent or refractory acute lymphoblastic or myeloblastic leukemia OR Chronic myelogenous leukemia with resistance to interferon alfa with any of the following: WBC at least 20,000/mm^3 after at least 3 months of interferon therapy At least 100% increase in WBC to at least 20,000/mm^3 confirmed over 2 weeks while receiving interferon alfa At least 66% Ph chromosome-positive cells after 1 year of interferon therapy At least 30% increase in number of Ph chromosome-positive cells after an interferon-induced response while continuing interferon therapy PATIENT CHARACTERISTICS: Age: Under 22 Performance status: Karnofsky 50-100% if over 10 years of age OR Lansky 50-100% if 10 years of age and under Life expectancy: At least 8 weeks Hematopoietic: See Disease Characteristics Hepatic: Bilirubin no greater than 1.5 times normal SGPT less than 3 times normal Albumin greater than 2 g/dL Renal: Creatinine no greater than 1.5 times normal OR Creatinine clearance or radioisotope glomerular filtration rate at least 70 mL/min Other: Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception If prior allogeneic stem cell transplantation, no uncontrolled graft-versus -host disease No seizure disorder if on anticonvulsants No uncontrolled infection No CNS toxicity greater than grade 2 PRIOR CONCURRENT THERAPY: Biologic therapy: See Disease Characteristics At least 1 week since prior biologic therapy and recovered At least 3 months since prior stem cell transplantation (SCT) At least 1 week since prior growth factors At least 1 week since prior interferon alfa Chemotherapy: Recovered from prior chemotherapy At least 6 weeks since prior busulfan and nitrosoureas At least 2 weeks since prior homoharringtonine At least 1 week since low-dose cytarabine At least 2 weeks since prior moderate-dose cytarabine At least 4 weeks since prior high-dose cytarabine At least 3 weeks since all other prior cytotoxic chemotherapies No prior hydroxyurea Endocrine therapy: Must be on a stable dose of steroids if received prior allogeneic SCT Radiotherapy: Recovered from prior radiotherapy At least 2 weeks since prior local palliative radiotherapy (small port) At least 6 months since prior craniospinal radiotherapy At least 6 months since prior radiotherapy to 50% or more of the pelvis At least 6 weeks since other prior substantial bone marrow radiotherapy Surgery: Not specified Other: No other concurrent investigational agents No concurrent anticonvulsants
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.4 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalGrupo II
ExperimentalGrupo III
ExperimentalGrupo IV
ExperimentalObjetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
Centros 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 235 ubicaciones
University of Alabama at Birmingham Comprehensive Cancer Center
Birmingham, United StatesAbrir University of Alabama at Birmingham Comprehensive Cancer Center en Google MapsUniversity of South Alabama Medical Center
Mobile, United StatesPhoenix Children's Hospital
Phoenix, United StatesArizona Cancer Center
Tucson, United States