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Total-Body Irradiation With or Without Fludarabine Phosphate Followed By Donor Stem Cell Transplant in Treating Patients With Hematologic Cancer

7 de abril de 2017 actualizado por: Brenda Sandmaier, Fred Hutchinson Cancer Center

A Multi-center Phase III Study Comparing Nonmyeloablative Conditioning With TBI Versus Fludarabine/TBI for HLA-matched Related Hematopoietic Cell Transplantation for Treatment of Hematologic Malignancies

This randomized phase III trial is studying total-body irradiation (TBI) and fludarabine phosphate to see how it works compared with TBI alone followed by donor stem cell transplant in treating patients with hematologic cancer. Giving low doses of chemotherapy, such as fludarabine phosphate, and radiation therapy before a donor stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune system cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after transplant may stop this from happening. It is not yet known whether TBI followed by donor stem cell transplant is more effective with or without fludarabine phosphate in treating hematologic cancer.

Descripción general del estudio

Descripción detallada

PRIMARY OBJECTIVES:

I. To compare overall survival at 3 years after conditioning with 200 cGy TBI alone vs. fludarabine (fludarabine phosphate)/200 cGy TBI in heavily pretreated patients with hematologic malignancies at low/moderate risk for graft rejection.

SECONDARY OBJECTIVES:

I. To compare the non-relapse mortality 1-year after conditioning in patients who received TBI alone vs. fludarabine/TBI.

II. To compare the incidences of graft rejection in patients who received TBI alone vs. fludarabine/TBI.

III. To compare the incidences of grades II-IV acute graft-versus-host disease (GVHD) and chronic extensive GVHD.

IV. To compare rates of disease progression and/or relapse-related mortality.

V. To compare the immune reconstitution and the risks of infections.

OUTLINE:

NONMYELOABLATIVE CONDITIONING REGIMEN: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive fludarabine phosphate intravenously (IV) on days -4 to -2. Patients then undergo low-dose TBI on day 0.

ARM II: Patients undergo low-dose TBI on day 0.

ALLOGENEIC PERIPHERAL BLOOD STEM CELL TRANSPLANTATION (PBSCT): After TBI, patients undergo PBSCT on day 0.

IMMUNOSUPPRESSION: Patients receive cyclosporine orally (PO) twice daily (BID) on days -3 to 56 in the absence of GVHD. Patients with no evidence of GVHD at day 56 begin a cyclosporine taper and continue the taper until day 180. Patients with evidence of disease progression and no evidence of GVHD prior to day 56 receive tapered doses of cyclosporine for 2 weeks. Patients also receive mycophenolate mofetil (MMF) PO BID on days 0-28 in the absence of GVHD. If treatment for GVHD is required before day 28, MMF is continued until a steroid taper begins.

Patients are followed up periodically for 1.5 years and then annually for 5 years post-transplantation.

Tipo de estudio

Intervencionista

Inscripción (Actual)

87

Fase

  • Fase 3

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Koln, Alemania, 50924
        • Medizinische Univ Klinik Koln
      • Leipzig, Alemania, D-04103
        • Universitaet Leipzig
      • Tuebingen, Alemania, D-72076
        • University of Tuebingen-Germany
    • Oregon
      • Medford, Oregon, Estados Unidos, 97504
        • OHSU Cancer Institute-Southern Region
    • Utah
      • Salt Lake City, Utah, Estados Unidos, 84112
        • Huntsman Cancer Institute/University of Utah
      • Salt Lake City, Utah, Estados Unidos, 84143
        • LDS Hospital
    • Washington
      • Seattle, Washington, Estados Unidos, 98109
        • Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
      • Seattle, Washington, Estados Unidos, 98101
        • VA Puget Sound Health Care System
    • Wisconsin
      • Milwaukee, Wisconsin, Estados Unidos, 53226
        • Froedtert and The Medical College of Wisconsin
      • Torino, Italia, 10126
        • University of Torino

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

No mayor que 75 años (Niño, Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Patients must be not eligible for conventional allogeneic hematopoietic cell transplantation (HCT) and must have disease expected to be stable for at least 100 days without chemotherapy
  • An autograft immediately prior (less than 6 months) to nonmyeloablative HCT (tandem approach) is not permitted
  • Patients with hematologic malignancies treatable with HCT or with a B cell malignancy except those curable with autologous transplant will be included
  • Aggressive non-Hodgkin lymphomas (NHLs) and other histologies such as diffuse large B cell NHL: patients are eligible IF they are not eligible for autologous hematopoietic stem cell transplantation (HSCT), not eligible for conventional myeloablative HSCT, or have failed an autologous HSCT
  • Low grade NHL with < 6 month duration of complete remission (CR) between courses of conventional therapy
  • Mantle cell NHL; may be treated in first CR
  • Chronic lymphocytic leukemia (CLL) must have either:

    • Failed to meet National Cancer Institute (NCI) Working Group criteria for complete or partial response after therapy with a regimen containing fludarabine phosphate (FLU) (or another nucleoside analog, e.g. cladribine [2-CDA], pentostatin) or experience disease relapse within 12 months after completing therapy with a regimen containing FLU (or another nucleoside analog)
    • Failed FLU-cyclophosphamide [CY]-rituximab (FCR) combination chemotherapy at any time point
    • Have "17p deletion" cytogenetic abnormality; patients should have received induction chemotherapy but could be transplanted in 1st CR
    • Or patients with a diagnosis of CLL (or small lymphocytic lymphoma) or diagnosis of CLL that progresses to prolymphocytic leukemia (PLL), or T-cell CLL or PLL
  • Hodgkin lymphoma (HL): must have received and failed frontline therapy; patients must have failed or were not eligible for autologous transplant
  • Multiple myeloma (MM): must have chemosensitive disease after failed autografting (an autografting immediately prior [within 6 months] to nonmyeloablative HCT [tandem approach] is not permitted)
  • Acute myeloid leukemia (AML): must have < 5% marrow blasts at the time of transplant and be beyond first CR
  • Acute lymphocytic leukemia (ALL): must have < 5% marrow blasts at the time of transplant and be beyond first CR
  • Chronic myelogenous leukemia (CML): patients will be accepted in chronic phase (CP) beyond CP1 if they have received previous myelosuppressive chemotherapy or HCT, < 5% marrow blasts at time of transplant
  • Myelodysplastic syndromes (MDS)/myeloproliferative disorders (MPD): must have received previous myelosuppressive chemotherapy or HCT, < 5% marrow blasts at time of transplant
  • Waldenstroms Macroglobulinemia: must have failed 2 courses of therapy
  • Patients will not be allowed to receive myelosuppressive chemotherapy for three weeks prior to conditioning
  • Patients < 12 years old must be approved by both the participating institutions' patient review committee such as the Patient Care Conference (PCC) at the Fred Hutchinson Cancer Research Center (FHCRC) and the FHCRC principal investigator
  • Patients who refused to be treated on a conventional HCT protocol; for this inclusion criterion, transplants must be approved by both the participating institution's patient review committee such as the Patient Care Conference (PCC) at the FHCRC and the FHCRC principal investigator
  • Patients with human leukocyte antigen (HLA)-matched related donors
  • DONOR: Related donor who is HLA genotypically identical at least at one haplotype and may be phenotypically or genotypically identical at the allele level at HLA-A, -B, -C, -DRB1, and -DQB1
  • DONOR: Donor must consent to filgrastim (G-CSF) administration and leukapheresis
  • DONOR: Donor must have adequate veins for leukapheresis or agree to placement of central venous catheter (femoral, subclavian)
  • DONOR: For females of child bearing age, serum pregnancy qualitative (PGSTAT) within 72 hours prior to initial dose of filgrastim (G-CSF); results must be available prior to filgrastim

Exclusion Criteria:

  • Eligible for a high priority curative autologous transplant
  • Patients with rapidly progressive, aggressive NHL unless in minimal disease state
  • Patients with chronic myelomonocytic leukemia
  • Presence of circulating leukemic blasts (in the peripheral blood) detected by standard pathology for patients with AML, ALL or CML
  • Life expectancy severely limited by diseases other than malignancy
  • Any current central nervous system (CNS) involvement with disease refractory to intrathecal chemotherapy
  • Fertile men or women unwilling to use contraceptives during and for up to 12 months post treatment
  • Female patients who are pregnant or breastfeeding
  • Human immunodeficiency virus (HIV) positive patients
  • Patients with active non-hematological malignancies (except localized non-melanoma skin malignancies)
  • 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
  • Fungal infections with radiological progression after receipt of amphotericin formulation or mold-active azoles for greater than 1 month
  • Patients with active bacterial or fungal infections unresponsive to medical therapy
  • Karnofsky score < 50 for adult patients
  • Lansky-Play performance score < 50 for pediatric patients
  • The addition of cytotoxic agents for "cytoreduction" with the exception of tyrosine kinase inhibitors (imatinib mesylate), cytokine therapy, hydroxyurea, low dose cytarabine, chlorambucil, or rituxan will not be allowed within three weeks of the initiation of conditioning
  • Patients with the following organ dysfunction:

    • Symptomatic coronary artery disease or ejection fraction < 35% or other cardiac failure requiring therapy (required for patients with history of cardiac disease or anthracycline use); ejection fraction is required if age > 50 years or there is a history of anthracycline exposure or history of cardiac disease
    • Poorly controlled hypertension on multiple antihypertensives
    • Pulmonary: diffusion capacity of carbon monoxide (DLCO) < 30%, total lung capacity (TLC) < 30%, forced expiratory volume in one second (FEV1) < 30% and/or receiving supplementary continuous oxygen; the FHCRC study principal investigator (PI) must approve enrollment of all patients with pulmonary nodules
    • Liver function abnormalities: patients with clinical or laboratory evidence of liver disease would be evaluated for the cause of liver disease, its clinical severity in terms of liver function, bridging fibrosis, and the degree of portal hypertension; patients will be excluded if they are 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 > 3 mg/dL, and symptomatic biliary disease
  • DONOR: Age less than 12 years
  • DONOR: Identical twin
  • DONOR: Pregnancy
  • DONOR: Infection with HIV
  • DONOR: Known allergy to filgrastim
  • DONOR: Current serious systemic illness that would result in increased risk for filgrastim mobilization and harvest of PBSC

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Arm I (chemotherapy, TBI, transplant, GVHD prophylaxis)
Patients receive fludarabine phosphate IV on days -4 to -2. Patients then undergo low-dose TBI on day 0. After TBI, patients undergo PBSCT on day 0. Patients receive cyclosporine PO BID on days -3 to 56 in the absence of GVHD. Patients with no evidence of GVHD at day 56 begin a cyclosporine taper and continue the taper until day 180. Patients with evidence of disease progression and no evidence of GVHD prior to day 56 receive tapered doses of cyclosporine for 2 weeks. Patients also receive MMF PO BID on days 0-28 in the absence of GVHD. If treatment for GVHD is required before day 28, MMF is continued until a steroid taper begins.
Orden de compra dada
Otros nombres:
  • Cellcept
  • Dos hombres y una mujer
Dado IV
Otros nombres:
  • 2-F-ara-AMP
  • Beneficio
  • SH T 586
Orden de compra dada
Otros nombres:
  • 27-400
  • CSA
  • Neoral
  • Sandimmun
  • OL 27-400
Someterse a un trasplante
Otros nombres:
  • Trasplante de PBPC
  • Trasplante de células progenitoras de sangre periférica
  • Soporte de células madre periféricas
  • Trasplante de células madre periféricas
Undergo TBI
Otros nombres:
  • Irradiación corporal total
  • LCT
  • Irradiación de cuerpo entero
Comparador activo: Arm II (TBI, transplant, GVHD prophylaxis)
Patients undergo low-dose TBI on day 0. After TBI, patients undergo PBSCT on day 0. Patients receive cyclosporine PO BID on days -3 to 56 in the absence of GVHD. Patients with no evidence of GVHD at day 56 begin a cyclosporine taper and continue the taper until day 180. Patients with evidence of disease progression and no evidence of GVHD prior to day 56 receive tapered doses of cyclosporine for 2 weeks. Patients also receive MMF PO BID on days 0-28 in the absence of GVHD. If treatment for GVHD is required before day 28, MMF is continued until a steroid taper begins.
Orden de compra dada
Otros nombres:
  • Cellcept
  • Dos hombres y una mujer
Orden de compra dada
Otros nombres:
  • 27-400
  • CSA
  • Neoral
  • Sandimmun
  • OL 27-400
Someterse a un trasplante
Otros nombres:
  • Trasplante de PBPC
  • Trasplante de células progenitoras de sangre periférica
  • Soporte de células madre periféricas
  • Trasplante de células madre periféricas
Undergo TBI
Otros nombres:
  • Irradiación corporal total
  • LCT
  • Irradiación de cuerpo entero

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall Survival
Periodo de tiempo: 3 years after transplant
Percentage of patients surviving as estimated by Kaplan-Meier.
3 years after transplant

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of Non-relapse Mortality
Periodo de tiempo: 3 years after transplant
Percentage of NRM as estimated by cumulative incidence methods with competing risks
3 years after transplant
Incidence of Relapse/Progression
Periodo de tiempo: 3 years after transplant
Percentage of relapse estimated by cumulative incidence methods
3 years after transplant
Incidence of Relapse-related Mortality
Periodo de tiempo: 3 years after transplant
Percentage of death following relapse/progression, estimated by cumulative incidence methods
3 years after transplant
Incidence of Grades II-IV Acute GVHD
Periodo de tiempo: 120 days after transplant
Percentage patients with grades II-IV GHVD, estimated by cumulative incidence methods
120 days after transplant
Incidence of Chronic Extensive GVHD
Periodo de tiempo: 3 years after transplant
Percentage patients with chronic extensive GVHD, estimated by cumulative incidence methods
3 years after transplant
Incidence of Graft Rejection
Periodo de tiempo: 1 year after transplant
Donor CD3 chimerism less than 5%
1 year after transplant
Progression-free Survival
Periodo de tiempo: 3 years after transplant
Percentage of patients with progression-free survival, estimated by cumulative incidence methods
3 years after transplant

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de octubre de 2003

Finalización primaria (Actual)

1 de febrero de 2014

Finalización del estudio (Actual)

2 de febrero de 2014

Fechas de registro del estudio

Enviado por primera vez

9 de enero de 2004

Primero enviado que cumplió con los criterios de control de calidad

11 de enero de 2004

Publicado por primera vez (Estimar)

12 de enero de 2004

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

15 de mayo de 2017

Última actualización enviada que cumplió con los criterios de control de calidad

7 de abril de 2017

Última verificación

1 de abril de 2017

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • 1813.00 (Otro identificador: Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium)
  • P30CA015704 (Subvención/contrato del NIH de EE. UU.)
  • P01CA078902 (Subvención/contrato del NIH de EE. UU.)
  • NCI-2009-01532 (Identificador de registro: CTRP (Clinical Trial Reporting Program))

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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