Anti-Leukemia Immune Responses After Irradiation of Extramedullary Tumors
Running, not enrolling · Early Phase 1
Conditions studied: Acute Myeloid Leukemia, Myeloid Leukemia, Recurrent Acute Myeloid Leukemia
In brief
This clinical trial assesses how the immune system responds to leukemia tumors after low dose radiation delivered as part of standard of care. The information learned in this study may help them know if adding immunotherapy (a type of treatment that uses the immune system to fight cancer) can be helpful in future leukemia patients receiving radiation.
Key facts
- Study ID
- NCT05035706
- Run by
- M.D. Anderson Cancer Center
- People needed
- 10
- Starts
- 2021-06-30
- Expected to finish
- 2026-04-30
- Last updated by the study team
- 2026-03-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients diagnosed with new or recurrent myeloid leukemia
- Aged >= 18 years old
- Eastern Cooperative Oncology Group (ECOG) performance status < 4
- Patient have measurable and amenable to biopsy under local anesthesia without the need for imaging directed procedure
- Ability to understand and provide signed informed consent
- Females must be surgically or biologically sterile or postmenopausal (amenorrhoeic for at least 12 months) or if of childbearing potential, must have a negative serum or urine pregnancy test within 72 hours before the start of the treatment. Women of childbearing potential must agree to use an adequate method of contraception during the study and until the last radiation treatment. Males must be surgically or biologically sterile or agree to use an adequate method of contraception during the study and until the last radiation treatment
You may not qualify if…
- Patients who are unwilling to participate
- Patients unwilling to undergo the biopsy before or after radiotherapy
Where it is running
- M D Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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