- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00118352
Alemtuzumab, Fludarabine Phosphate, and Total-Body Irradiation Followed by Cyclosporine and Mycophenolate Mofetil in Treating Patients Who Are Undergoing Donor Stem Cell Transplant for Hematologic Cancer
Campath (Alemtuzumab) Dose Escalation, Low-Dose TBI and Fludarabine Followed by HLA Class II Mismatched Donor Stem Cell Transplantation for Patients With Hematologic Malignancies: A Multicenter Trial
Descripción general del estudio
Estado
Condiciones
- Leucemia mielomonocítica crónica
- Leucemia mieloide aguda recurrente en adultos
- Leucemia mielomonocítica juvenil
- Linfoma de células B de la zona marginal extraganglionar del tejido linfoide asociado a la mucosa
- Linfoma de células B de la zona marginal ganglionar
- Linfoma de Burkitt en adultos recidivante
- Linfoma difuso de células grandes en adultos recidivante
- Linfoma difuso de células mixtas en adultos recidivante
- Linfoma difuso de células pequeñas hendidas en adultos recidivante
- Linfoma inmunoblástico de células grandes en adultos recidivante
- Linfoma linfoblástico recidivante en adultos
- Linfoma folicular de grado 1 recidivante
- Linfoma folicular de grado 2 recidivante
- Linfoma folicular de grado 3 recidivante
- Linfoma de células del manto recidivante
- Linfoma recidivante de la zona marginal
- Linfoma de la zona marginal esplénica
- Macroglobulinemia de Waldenström
- Leucemia mieloide aguda en adultos en remisión
- Leucemia mieloide aguda infantil en remisión
- Linfoma periférico de células T
- Linfoma anaplásico de células grandes
- Linfoma angioinmunoblástico de células T
- Leucemia linfoblástica aguda en adultos en remisión
- Linfoma de células T/NK extraganglionar de tipo nasal en adultos
- Leucemia linfoblástica aguda infantil en remisión
- Leucemia mielógena crónica infantil
- Síndromes mielodisplásicos infantiles
- Leucemia mielógena crónica en fase crónica
- Linfoma no Hodgkin cutáneo de células B
- Linfoma hepatoesplénico de células T
- Linfoma intraocular
- Síndromes mielodisplásicos tratados previamente
- Leucemia linfoblástica aguda recurrente en adultos
- Granulomatosis linfomatoide recurrente de grado III del adulto
- Linfoma de Hodgkin en adultos recidivante
- Leucemia/linfoma de células T del adulto recurrente
- Leucemia linfoblástica aguda infantil recurrente
- Leucemia mieloide aguda infantil recurrente
- Linfoma no Hodgkin cutáneo de células T recidivante
- Micosis Fungoide Recurrente/Síndrome de Sézary
- Linfoma de linfocitos pequeños recidivante
- Mieloma múltiple refractario
- Leucemia mielógena crónica recidivante
- Síndromes mielodisplásicos secundarios
- Linfoma de intestino delgado
- Linfoma testicular
- Leucemia linfocítica crónica refractaria
- Leucemia de células pilosas refractaria
- Leucemia aguda indiferenciada
- Leucemia mieloide crónica atípica, BCR-ABL1 negativo
- Leucemia de mastocitos
- Neoplasia mielodisplásica/mieloproliferativa, inclasificable
- Linfoma difuso de células grandes infantil
- Linfoma inmunoblástico de células grandes infantil
- Linfoma de células T/NK extraganglionar de tipo nasal infantil
- Linfoma anaplásico de células grandes infantil recidivante
- Granulomatosis linfomatoide grado III infantil recurrente
- Linfoma de células grandes infantil recidivante
- Linfoma linfoblástico infantil recidivante
- Linfoma de células pequeñas no hendidas infantil recidivante
- Linfoma de Hodgkin infantil recidivante/refractario
- Linfoma de Burkitt infantil
- Linfoma extraganglionar no cutáneo
Intervención / Tratamiento
- Otro: análisis de biomarcadores de laboratorio
- Droga: fosfato de fludarabina
- Procedimiento: trasplante de células madre de sangre periférica
- Droga: micofenolato de mofetilo
- Biológico: alemtuzumab
- Radiación: irradiación corporal total
- Droga: ciclosporina
- Procedimiento: trasplante alogénico de células madre hematopoyéticas
- Biológico: graft versus host disease prophylaxis/therapy
Descripción detallada
PRIMARY OBJECTIVES:
I. To determine which dose of Campath (alemtuzumab) allows related and unrelated human leukocyte antigen (HLA) class-II mismatched hematopoietic cell transplantation (HCT) with an incidence of grade III-IV acute graft-versus-host disease (GVHD) less than 40%.
SECONDARY OBJECTIVES:
I. Incidence of graft rejection.
II. Number of days of steroids >= 1mg/kg required before day 100 in each patient.
III. Incidence of non-relapse mortality.
IV. Risk/incidence of infections.
V. Immune reconstitution.
VI. Risk for disease progression and relapse.
OUTLINE: This is a dose-escalation study of alemtuzumab.
NONMYELOABLATIVE CONDITIONING REGIMEN: Patients receive alemtuzumab intravenously (IV) over 6 hours once daily on days -6, -5, and -4 OR days -5 and -4 and fludarabine phosphate IV over 30 minutes on days -4, -3, and -2. Patients also undergo low-dose total-body irradiation (TBI) on day 0.
ALLOGENEIC PERIPHERAL BLOOD STEM CELL TRANSPLANTATION (PBSCT): After completion of TBI, patients undergo allogeneic PBSCT on day 0.
IMMUNOSUPPRESSION: Patients receive cyclosporine orally (PO) or IV every 12 hours on days -3 to 180 followed by a taper until day 365 in the absence of GVHD. Beginning 4-6 hours after completion of allogeneic PBSCT, patients receive mycophenolate mofetil PO every 8 hours on days 0 to 100 followed by a taper until day 156 in the absence of GVHD.
After completion of study treatment, patients are followed up periodically for 12 months, at 18 months, and then annually for 5 years.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 2
Contactos y Ubicaciones
Ubicaciones de estudio
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Washington
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Seattle, Washington, Estados Unidos, 98109
- Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
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Torino, Italia, 10126
- University of Torino
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- The patient must be not eligible for conventional transplants and must have disease expected to be stable for at least 100 days without chemotherapy
Patients with hematologic malignancies treatable with HCT will be included:
- Aggressive non-Hodgkin lymphomas (NHLs) and other histologies such as diffuse large B-cell NHL: not eligible for autologous HCT, not eligible for conventional myeloablative HCT, or after failed autologous HCT;
- Low grade NHL: with < 6 month duration of complete response (CR) between courses of conventional therapy;
- Mantle cell NHL: may be treated in first CR;
- Chronic lymphocytic leukemia (CLL): must have failed 2 lines of conventional therapy and must be refractory to fludarabine; this includes patients who fail to have a complete or partial response after therapy with a regimen containing fludarabine (or another nucleoside analog] or experience disease relapse within 12 months after completing therapy with a regimen containing fludarabine [or another nucleoside analog);
- Hodgkin's disease (HD): must have received and failed frontline therapy and have failed or were not eligible for autologous transplant;
- Multiple myeloma (MM): must have received prior chemotherapy or failed autografting; following a planned autologous transplant [tandem] is allowed;
- Acute myeloid leukemia (AML): must have < 5% marrow blasts at the time of transplant;
- Acute lymphocytic leukemia (ALL): must have < 5% marrow blasts at the time of transplant;
- Chronic myelogenous leukemia (CML): patients will be accepted beyond first clinical progression (CP1) if they have received previous myelosuppressive chemotherapy or HCT, and have < 5% marrow blasts at time of transplant;
- Myelodysplastic syndrome/myeloproliferative disease (MDS/MPD): must have failed previous myelosuppressive chemotherapy or HCT, and have < 5% marrow blasts at time of transplant;
- Waldenstrom's macroglobulinemia: must have failed 2 courses of therapy
- Patient refuses to be treated on a conventional transplant protocol; for this inclusion criteria, transplants must be approved by both the participating institution's patient review committee, such as the Patient Care Conference (PCC) at the Fred Hutchinson Cancer Research Center (FHCRC), and the FHCRC principal investigator
Patient with related or unrelated donors for whom:
- There is a likelihood of disease progression while HLA typing and results of a preliminary search and the donor pool suggest that a 10/10 HLA-A, B, C, DRB1 and DQB1 matched unrelated donor will not be found;
- Patient and donor must be matched for at least one DRB1 allele and one DQB1 allele;
- Best available matches are HLA class I HLA-A, -B, -C allele matched donors allowing for any one or two DRB1 and/or DQB1 antigen/allele mismatch;
- There is no indication for an autologous transplantation as a treatment option
- DONOR: For HLA matching inclusion criteria, see patient inclusion criteria
- DONOR: Only peripheral blood stem cells (PBSC) will be permitted as a HSC source on this protocol
Exclusion Criteria:
- Positive crossmatch between donor and recipients
- Patient's life expectancy is severely limited by diseases other than malignancy
- Patient has central nervous system (CNS) involvement with disease refractory to intrathecal chemotherapy
- Presence of circulating leukemic blasts (in the peripheral blood) detected by standard pathology for patients with AML, ALL or CML
- Patient is a fertile man or woman unwilling to use contraceptives during and for up to 12 months post treatment
- Patient is a female who is pregnant or breastfeeding
- Patient is human immunodeficiency virus (HIV) positive
- Patients with active non-hematologic malignancies (except non-melanoma skin cancers)
- Patients with a history of non-hematologic malignancies (except non-melanoma skin cancers) currently in a complete remission, who are less than 5 years from the time of complete remission, and have a > 20% risk of disease recurrence
- Patient has a fungal infection with radiological progression after receipt of amphotericin B or active triazole for greater than 1 month
Patient has the following organ dysfunction:
- Symptomatic coronary artery disease or ejection fraction < 35% or other cardiac failure requiring therapy; ejection fraction is required if age > 50 years or if the patient has a history of anthracyclines or history of cardiac disease;
- Diffusion capacity of the lung for carbon monoxide (DLCO) < 35% total lung capacity (TLC) < 35%, forced expiratory volume of the lung in one second (FEV1) < 35% and/or receiving supplementary continuous oxygen; the FHCRC study principal investigator (PI) must approve enrollment of all patients with pulmonary nodules;
- Liver function abnormalities: patient with clinical or laboratory evidence of liver disease will be evaluated for the cause of liver disease, its clinical severity in terms of liver function, bridging fibrosis, and the degree of portal hypertension; the patient will be excluded if he/she is found to have fulminant liver failure, cirrhosis of the liver with evidence of portal hypertension, alcoholic hepatitis, esophageal varices, a history of bleeding esophageal varices, hepatic encephalopathy, uncorrectable hepatic synthetic dysfunction evinced by prolongation of the prothrombin time, ascites related to portal hypertension, bacterial or fungal liver abscess, biliary obstruction, chronic viral hepatitis with total serum bilirubin > 3mg/dL, or symptomatic biliary disease
- Patient has poorly controlled hypertension and on multiple antihypertensives
- Karnofsky performance score < 70 for adult patients
- Lansky play-performance score < 70 for pediatric patients
- Patient received cytotoxic agents for "cytoreduction" within three weeks (or the interval in which a cycle of standard chemotherapy would be administered in a non-transplant setting) prior to initiating the nonmyeloablative transplant conditioning; (exceptions are hydroxyurea and imatinib mesylate)
- DONOR: Marrow donors
- DONOR: Positive crossmatch between donor and recipient
- DONOR: Donor is HIV-positive and/or has a medical condition that would result in increased risk for filgrastim (G-CSF) mobilization and harvest of PBSC
- DONOR: Donor age < 12 years
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Treatment (chemotherapy, TBI, transplant)
NONMYELOABLATIVE CONDITIONING REGIMEN: Patients receive alemtuzumab IV over 6 hours once daily on days -6, -5, and -4 OR days -5 and -4 and fludarabine phosphate IV over 30 minutes on days -4, -3, and -2. Patients also undergo low-dose TBI on day 0. ALLOGENEIC PBSCT: After completion of TBI, patients undergo allogeneic PBSCT on day 0. IMMUNOSUPPRESSION: Patients receive cyclosporine PO or IV every 12 hours on days -3 to 180 followed by a taper until day 365 in the absence of GVHD. Beginning 4-6 hours after completion of allogeneic PBSCT, patients receive mycophenolate mofetil PO every 8 hours on days 0 to 100 followed by a taper until day 156 in the absence of GVHD. |
Estudios correlativos
Dado IV
Otros nombres:
Someterse a PBSCT
Otros nombres:
Orden de compra dada
Otros nombres:
Dado IV
Otros nombres:
Someterse a una TBI de dosis baja
Otros nombres:
Dado PO o IV
Otros nombres:
Someterse a un trasplante alogénico de células madre
Undergo GVHD prophylaxis/therapy
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Incidence of Grade III-IV Acute GVHD
Periodo de tiempo: 100 days after transplant
|
Severity of Individual Organ Involvement Liver: Stage 2 - bilirubin (3-5.9mg/100ml) Stage 3 - bilirubin (6-14.9mg/100ml) Stage 4 - bilirubin > 15mg/100ml Gut: Diarrhea is graded stage 1 to stage 4 in severity. Nausea and vomiting and/or anorexia caused by GVHD is assigned as stage 1 in severity. The severity of gut involvement is assigned to the most severe involvement noted. Patients with visible bloody diarrhea are at least stage 2 gut and grade 3 overall Severity of GVHD Grade III - Stage 2 to 4 gastrointestinal involvement and/or Stage 2 to 4 liver involvement with or without a rash Grade IV - Pattern and severity of GVHD similar to grade 3 with extreme constitutional symptoms or death |
100 days after transplant
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Incidence of Graft Rejection
Periodo de tiempo: 84 days after transplant
|
Percentage patients that experienced graft rejection.
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84 days after transplant
|
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Incidence of High-dose Corticosteroid Utilization.
Periodo de tiempo: 100 days after transplant
|
Percentage patients requiring steroids greater than 1 mg/kg.
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100 days after transplant
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Incidence of Non-relapse Mortality
Periodo de tiempo: 100 days after transplant
|
Percentage patient deaths due to non-relapse mortality
|
100 days after transplant
|
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Incidence of Infection
Periodo de tiempo: Up to 5 years post-transplant
|
Percentage patients that experienced infection(s).
|
Up to 5 years post-transplant
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Immune Reconstitution
Periodo de tiempo: Up to 1 year post-transplant
|
The outcome of immune reconstitution was not analyzed by the collaborating laboratory because only a small number of patients were only enrolled in Dose Level 1 (no alemtuzumab).
The Dose Level 1 patients were going to be the baseline for which to compare the other patients on Dose Level 2 (and 3) who would have received alemtuzumab.
The collaborating investigator determined that the study was not worthwhile performing based on this information.
|
Up to 1 year post-transplant
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Disease Progression/Relapse
Periodo de tiempo: Up to 5 years
|
CML New cytogenetic abnormality and/or development of accelerated phase or blast crisis. The criteria for accelerated phase will be defined as unexplained fever greater than 38.3°C, new clonal cytogenetic abnormalities in addition to a single Ph-positive chromosome, marrow blasts and promyelocytes >20%. AML, ALL >5% marrow blasts by morphologic or flow cytometric, or appearance of extramedullary disease. CLL ≥1 of: Physical exam/Imaging studies (nodes, liver, and/or spleen) ≥50% increase or new, circulating lymphocytes by morphology and/or flow cytometry ≥50% increase, and lymph node biopsy w/ Richter's transformation. NHL >25% increase in the sum of the products of the perpendicular diameters of marker lesions, or the appearance of new lesions. MM ≥100% increase of the serum myeloma protein from its lowest level, or reappearance of myeloma peaks that had disappeared w/ treatment; or definite increase in the size or number of plasmacytomas or lytic bone lesions. |
Up to 5 years
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Procesos Patológicos
- Enfermedades cardiovasculares
- Enfermedades Vasculares
- Enfermedades virales
- Infecciones
- Enfermedades del sistema inmunológico
- Neoplasias De Tejidos Conectivos Y Blandos
- Neoplasias por tipo histológico
- Neoplasias
- Trastornos linfoproliferativos
- Enfermedades linfáticas
- Trastornos inmunoproliferativos
- Neoplasias por sitio
- Atributos de la enfermedad
- Enfermedad
- Enfermedades de la médula ósea
- Enfermedades hematológicas
- Trastornos hemorrágicos
- Trastornos hemostáticos
- Paraproteinemias
- Trastornos de proteínas en sangre
- Infecciones por virus de ADN
- Infecciones bacterianas y micosis
- Infecciones por virus tumorales
- Neoplasias De Células Plasmáticas
- Condiciones precancerosas
- Infecciones por el virus de Epstein-Barr
- Infecciones por herpesviridae
- Leucemia de células B
- Neoplasias Del Tejido Conectivo
- Neoplasias Oculares
- Linfadenopatía
- Mastocitosis Sistémica
- Mastocitosis
- Linfoma
- Linfoma Folicular
- Linfoma de células B
- Linfoma de células B grandes, difuso
- Síndrome
- Síndromes mielodisplásicos
- Mieloma múltiple
- Leucemia
- Leucemia Mieloide
- Leucemia Mieloide Aguda
- Enfermedad de Hodgkin
- Reaparición
- Linfoma No Hodgkin
- Preleucemia
- Leucemia Mielomonocítica Aguda
- Leucemia Mielomonocítica Crónica
- Leucemia Mielomonocítica Juvenil
- Micosis
- Linfoma de Burkitt
- Linfoma De Células Del Manto
- Linfoma, Células B, Zona Marginal
- Leucemia-linfoma linfoblástico de células precursoras
- Linfoma De Células Grandes Inmunoblástico
- Linfoma plasmablástico
- Macroglobulinemia de Waldenström
- Leucemia Linfocítica Crónica De Células B
- Leucemia Linfoide
- Linfoma de células T
- Linfoma De Células T Periférico
- Leucemia, Mielógena, Crónica, BCR-ABL Positivo
- Leucemia mieloide en fase crónica
- Linfoma, De Células T, Cutáneo
- Leucemia de células T
- Leucemia-linfoma de células T adultas
- Micosis Fungoide
- Síndrome de Sézary
- Linfoma Anaplásico De Células Grandes
- Granulomatosis linfomatoide
- Linfoma Extraganglionar De Células NK-T
- Linfoma intraocular
- Linfadenopatía inmunoblástica
- Trastornos mieloproliferativos
- Enfermedades mielodisplásicas-mieloproliferativas
- Leucemia De Células Peludas
- Leucemia, mieloide, crónica, atípica, BCR-ABL negativa
- Leucemia de mastocitos
- Efectos fisiológicos de las drogas
- Mecanismos moleculares de acción farmacológica
- Agentes antiinfecciosos
- Inhibidores de enzimas
- Agentes antirreumáticos
- Antimetabolitos, Antineoplásicos
- Antimetabolitos
- Agentes antineoplásicos
- Agentes inmunosupresores
- Factores inmunológicos
- Agentes dermatológicos
- Agentes antibacterianos
- Antibióticos, Antineoplásicos
- Agentes antifúngicos
- Agentes antituberculosos
- Antibióticos, Antituberculosos
- Inhibidores de calcineurina
- Anticuerpos
- Inmunoglobulinas
- Anticuerpos Monoclonales
- Agentes antineoplásicos inmunológicos
- Fludarabina
- Fosfato de fludarabina
- Ácido micofenólico
- Ciclosporina
- Ciclosporinas
- Alemtuzumab
Otros números de identificación del estudio
- 1959.00 (Otro identificador: Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium)
- P30CA015704 (Subvención/contrato del NIH de EE. UU.)
- NCI-2009-01496 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
- P01CA018029 (Subvención/contrato del NIH de EE. UU.)
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