Autologous Transplant Using Dose-Escalated Total Body Irradiation & Cyclophosphamide & Palifermin for NHL
Phase I Study of Autologous Transplant Conditioned by Dose-Escalated Total Body Irradiation (TBI) and Standard Doses of Cyclophosphamide and Palifermin (Kepivance) for High Risk Non-Hodgkins Lymphoma
Most participants with a relapsed or refractory non-Hodgkin's lymphoma that receive an autologous transplant are likely to suffer a relapse because standard myeloablative preparative regimens are unable to produce a cure. The majority of these participants do not have a stem cell donor available, are too frail to undergo an allogeneic transplant, or refuse an allograft. Historically these participants with high risk non-Hodgkin's lymphoma have had a very poor outcome.
To take advantage of the low transplant related mortality associated with an autologous transplantation, the investigators propose modifying the preparative regimen to make it more effective without increasing toxicity. By increasing the dose of radiation while administering the protective growth factor palifermin (Kepivance), the investigators hope to decrease the risk of relapse without increasing transplant related mortality.
Three prospective randomized trials have studied different radiation schemes as a part of the TBI and cytoxan preparative regimen prior to allogeneic transplantation for patients with AML or CML. As a group these trials showed that higher doses of TBI in these older studies decreased the risk of relapse at the expense of VOD, GVHD, and CMV. Three retrospective studies have also postulated that higher dose radiation led to less risk of relapse.
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
This is a non-randomized, open-label phase I trial in participants with non-Hodgkin's lymphoma. The preparative regimen will be as follows:
Day -10 (prior to transplant) Palifermin treatment to prevent mouth sores Day -9 Palifermin treatment to prevent mouth sores Day -8 Palifermin treatment to prevent mouth sores Day -7 Total Body Irradiation twice a day Day -6 Total Body Irradiation twice a day Day -5 Total Body Irradiation twice a day Day -4 Total Body Irradiation twice a day Day -3 Cytoxan chemotherapy infusion Day -2 Cytoxan chemotherapy infusion Day -1 Day of rest Day 0 Stem cell infusion (bone marrow transplant), Palifermin treatment to prevent mouth sores and G-CSF given daily until stem cells take hold (engraftment) occurs.
Day +1 Palifermin treatment to prevent mouth sores Day +2 Palifermin treatment to prevent mouth sores
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Illinois
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Maywood, Illinois, Estados Unidos, 60153
- Patrick Stiff, MD
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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:
- Age 18 years of age or older
- Participants scheduled to undergo autologous stem cell transplantation with relapsed or refractory non-Hodgkin's Lymphoma with less than a partial remission to salvage therapy.
- Participants scheduled to undergo autologous stem cell transplantation with relapsed or refractory non-Hodgkin's Lymphoma with any site of disease 2 cm or greater on pre-transplant imaging.
- Participants must have a performance status (PS) of 0-1.
- Participants must have acceptable kidney function.
- Acceptable pulmonary function test of the lungs.
- Acceptable liver function tests.
Exclusion Criteria:
- Participants must not have cutaneous T-cell, mantle cell, or lymphoblastic lymphoma.
- Participants must not have prior peripheral blood or marrow transplantation.
- Participants must not have prior radiation.
- Participants must not have significant history of uncontrolled cardiac disease; for example, uncontrolled hypertension, unstable angina, recent myocardial infarction (within prior 6 months), uncontrolled congestive heart failure, and cardiomyopathy with decreased ejection fraction.
- Participants must not have active bacterial, fungal, or viral infection.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Dose Level 1
The participants will receive Palifermin on Day -10, -9 and -8.
Total Body Irradiation 1.64 Gy per Fraction for a total of 8 Fractions.
The total amount would be 13.12
Gy.
The participants will receive total body irradiation twice a day for four days (Day -7, -6, -5, and Day -4).
Over the following two days, the participants will receive cyclophosphamide (Day -3 and -2).
The participants will receive stem cell infusion on Day 0 and G-CSF given daily until engraftment occurs.
Participants will receive Palifermin on Day 0, +1 and +2.
|
When radiation is given in a way to cover the whole body, it is called total body irradiation.
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Experimental: Dose Level 2
The participants will receive Palifermin on Day -10, -9 and -8.
Total Body Irradiation 1.76 Gy per Fraction for a total of 8 Fractions.
The total amount would be 14.08 Gy.
The participants will receive total body irradiation twice a day for four days (Day -7, -6, -5, and Day -4).
Over the following two days, the participants will receive cyclophosphamide (Day -3 and -2).
The participants will receive stem cell infusion on Day 0 and G-CSF given daily until engraftment occurs.
Participants will receive Palifermin on Day 0, +1 and +2.
|
When radiation is given in a way to cover the whole body, it is called total body irradiation.
|
|
Experimental: Dose Level 3
The participants will receive Palifermin on Day -10, -9 and -8.
Total Body Irradiation 1.88 Gy per Fraction for a total of 8 Fractions.
The total amount would be 15.04 Gy.
The participants will receive total body irradiation twice a day for four days (Day -7, -6, -5, and Day -4).
Over the following two days, the participants will receive cyclophosphamide (Day -3 and -2).
The participants will receive stem cell infusion on Day 0 and G-CSF given daily until engraftment occurs.
Participants will receive Palifermin on Day 0, +1 and +2.
|
When radiation is given in a way to cover the whole body, it is called total body irradiation.
|
|
Experimental: Dose Level 4
The participants will receive Palifermin on Day -10, -9 and -8.
Total Body Irradiation 2.00 Gy per Fraction for a total of 8 Fractions.
The total amount would be 16 Gy.
The participants will receive total body irradiation twice a day for four days (Day -7, -6, -5, and Day -4).
Over the following two days, the participants will receive cyclophosphamide (Day -3 and -2).
The participants will receive stem cell infusion on Day 0 and G-CSF given daily until engraftment occurs.
Participants will receive Palifermin on Day 0, +1 and +2.
|
When radiation is given in a way to cover the whole body, it is called total body irradiation.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Determine the frequency and severity of adverse events by evaluating grade 3 and grade 4 adverse events.
Periodo de tiempo: 4 weeks
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Any grade 3 or 4 dose limiting toxicities as described : • Heart failure with only minor response to medical therapy
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4 weeks
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Blood work will be used to evaluate recovery of white blood cells, red blood cells and platelets.
Periodo de tiempo: 4 weeks
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To evaluate labwork during treatment and for 28 days post treatment
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4 weeks
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Pulmonary Function Test will be used to evaluate side effects of total body irradiation
Periodo de tiempo: 1 year
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Pulmonary Function Test will be used to evaluate side effects of total body irradiation.
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1 year
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CT scan or physical exam will be used to evaluate progression free survival.
Periodo de tiempo: 1 year
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CT scan or physical exam will be used to evaluate progression free survival as deemed necessary.
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1 year
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Mucositis measured by investigators.
Periodo de tiempo: At the start of treatment and daily until mucositis resolves or 28 days post transplant whichever comes first.
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Mucositis physical examination done by investigators by accessing the mouth using the WHO (World Health Organization) oral toxicity scale.
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At the start of treatment and daily until mucositis resolves or 28 days post transplant whichever comes first.
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Number of participants with Grade 4 through 5 Adverse Events that are related to study treatment, grading according to NCI CTCAE Version 3.
Periodo de tiempo: 28 days post treatment
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Dose-limiting toxicities that are probably or definitely related to the treatment regimen.
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28 days post treatment
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Mucositis measured by oral mucositis questionnaires
Periodo de tiempo: At the start of treatment and daily until mucositis resolves or 28 days post transplant whichever comes first.
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The participants will complete the oral mucositis daily questionnaires prior to the physical assessment.
The questionnaire includes the participants self-reported mouth and throat soreness.
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At the start of treatment and daily until mucositis resolves or 28 days post transplant whichever comes first.
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Patrick Stiff, MD, Loyola University
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
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 108993
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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