Leukemia Clinical Trial
Official title:
A Prospective Randomized Comparative Study of the Effect on Infections of Radiated Prophylactic White Cell Transfusions Versus Therapeutic Radiated White Cell Transfusions
Patients with leukemia often have low white blood cell counts after chemotherapy, which puts
them at greater risk for infection. The standard of care for preventing infections is to
give these patients antibiotic, antifungal, and antiviral drugs during the time that white
blood cell counts are low. However, many patients still develop infections during
chemotherapy. Radiated white blood cell transfusions are a standard treatment once a patient
develops a severe infection.
The goal of this clinical research study is to learn if giving unirradiated white blood cell
transfusions early in chemotherapy might delay or prevent infections in patients with
leukemia. Researchers also want to learn more about the type and severity of any infections
that do occur.
Study Groups:
If you are found to be eligible to take part of this study, and you are 1 of the first 60
participants to be enrolled, you will be randomly assigned (as in the flip of a coin) to 1
of 2 groups:
- If you are in Group 1, you will receive the standard of care drugs that are used to
prevent infections. You will also receive unirradiated white blood cell transfusions
2-3 times each week. If at any point you develop an infection, white blood cell
transfusions will then be given daily in addition to the standard treatment for the
infection.
- If you are in Group 2, you will receive the standard of care drugs that are used to
prevent infections. You will only receive unirradiated white blood cell transfusions if
at any point you develop an infection. You will receive these transfusions daily, in
addition to the standard treatment for the infection.
If you are not 1 of the first 60 participants to be enrolled, you will be assigned to the
study group that the study doctor decides is in your best interest. This will be decided
based on how the first participants have responded to the different treatments.
The drugs you receive as part of the standard therapy will be up the study doctor.
Study Procedures:
During each white blood cell transfusion, you will receive white blood cells from a
volunteer donor through a needle in your vein. Each transfusion will take anywhere from 1
hour to several hours, depending on how you tolerate the treatment.
Before each white blood cell transfusion, your vital signs will be recorded. During and for
1 hour after the transfusion, you will be monitored for side effects. You may be given a
drug to help or reduce any side effects. Your doctor will tell you more about any drug that
is given for side effects.
While you are in the hospital for leukemia treatment, blood (about 1 teaspoon) will be drawn
to check for fungal infections 2-3 times each week. This test will be done 1 time each week
when you are not in the hospital until the doctor no longer thinks it is needed.
If at any point you develop a fever while on study, blood (about 1 teaspoon) will be drawn
to check for infection. You will also have a CT scan within 3 days of developing a fever. If
the doctor thinks it is needed, you will then have a CT scan 2 weeks later and at any other
point that the doctor thinks it is needed to check for infection.
Length of Study:
You will continue to have transfusions until the doctor thinks infection has been controlled
or until your white blood cell counts stay at a certain level for at least 2 days in a row.
If at any point you are discharged from the hospital and your doctor wants you to continue
receiving white blood cell transfusions, you will be able to receive them as an outpatient.
You will be monitored for side effects and signs of infection for up to 2 cycles of
anti-leukemia treatment through a review of your medical record. You will be taken off study
if you have intolerable side effects.
This is an investigational study. Radiated white blood cell transfusions are considered to
be a standard procedure for the treatment of serious infections. It is investigational to
give unirradiated white blood cell transfusions as a way of preventing infections.
Up to 240 patients will take part in this study. All will be enrolled at MD Anderson.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05691608 -
MoleculAr Profiling for Pediatric and Young Adult Cancer Treatment Stratification 2
|
N/A | |
| Recruiting |
NCT04092803 -
Virtual Reality as a Distraction Technique for Performing Lumbar Punctures in Children and Young Adu
|
N/A | |
| Active, not recruiting |
NCT02530463 -
Nivolumab and/or Ipilimumab With or Without Azacitidine in Treating Patients With Myelodysplastic Syndrome
|
Phase 2 | |
| Completed |
NCT00948064 -
Vorinostat in Combination With Azacitidine in Patients With Newly-Diagnosed Acute Myelogenous Leukemia (AML) or Myelodysplastic Syndrome (MDS)
|
Phase 2 | |
| Completed |
NCT04474678 -
Quality Improvement Project - "My Logbook! - I Know my Way Around!"; ("Mein Logbuch - Ich Kenne Mich Aus!")
|
N/A | |
| Terminated |
NCT00801931 -
Double Cord Blood Transplant for Patients With Malignant and Non-malignant Disorders
|
Phase 1/Phase 2 | |
| Recruiting |
NCT03948529 -
RevErsing Poor GrAft Function With eLtrombopag After allogeneIc Hematopoietic Cell trAnsplantation
|
Phase 2 | |
| Completed |
NCT01682226 -
Cord Blood With T-Cell Depleted Haplo-identical Peripheral Blood Stem Cell Transplantation for Hematological Malignancies
|
Phase 2 | |
| Completed |
NCT00003270 -
Chemotherapy, Radiation Therapy, and Umbilical Cord Blood Transplantation in Treating Patients With Hematologic Cancer
|
Phase 2 | |
| Active, not recruiting |
NCT02723994 -
A Phase 2 Study of Ruxolitinib With Chemotherapy in Children With Acute Lymphoblastic Leukemia
|
Phase 2 | |
| Terminated |
NCT02469415 -
Pacritinib for Patients With Lower-Risk Myelodysplastic Syndromes (MDS)
|
Phase 2 | |
| Recruiting |
NCT04856215 -
90Y-labelled Anti-CD66 ab in Childhood High Risk Leukaemia
|
Phase 2 | |
| Recruiting |
NCT06155188 -
Post-transplant PT/FLU+CY Promotes Unrelated Cord Blood Engraftment in Haplo-cord Setting in Childhood Leukemia
|
N/A | |
| Completed |
NCT00001637 -
Immunosuppressive Preparation Followed by Blood Cell Transplant for the Treatment of Blood Cancers in Older Adults
|
Phase 2 | |
| Active, not recruiting |
NCT04188678 -
Resiliency in Older Adults Undergoing Bone Marrow Transplant
|
N/A | |
| Completed |
NCT02910583 -
Ibrutinib Plus Venetoclax in Subjects With Treatment-naive Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma (CLL/SLL)
|
Phase 2 | |
| Completed |
NCT01212926 -
Early Detection of Anthracycline Cardiotoxicity by Echocardiographic Analysis of Myocardial Deformation in 2D Strain
|
N/A | |
| Terminated |
NCT00014560 -
Antibody Therapy in Treating Patients With Refractory or Relapsed Non-Hodgkin's Lymphoma or Chronic Lymphocytic Leukemia
|
Phase 1 | |
| Recruiting |
NCT04977024 -
SARS-CoV-2 Vaccine (GEO-CM04S1) Versus mRNA SARS-COV-2 Vaccine in Patients With Blood Cancer
|
Phase 2 | |
| Recruiting |
NCT05866887 -
Insomnia Prevention in Children With Acute Lymphoblastic Leukemia
|
N/A |