Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Linda Elias, RN
CONTACT
Amy Rodger, RN
CONTACT
Lead
Sawa Ito, MD
With
This novel regimen has the potential to address a significant unmet need for this high-risk population of patients who have few, if any, effective therapeutic options. In Cohort 1, if this trial confirms the clinical efficacy of IFN-γ/DLI in patients with relapsed AML/MDS after HLA-matched alloSCT, it may establish a new therapeutic approach for post-transplant AML/MDS relapse. Cohort 2 will further evaluate the safety and potential efficacy of IFN-γ/DLI in patients with relapsed AML/MDS after haploidentical alloSCT, where treatment options are also limited and the risk of GVHD requires careful assessment. Together, these cohorts would provide a rationale to explore additional indications for IFN-γ in the context of alloSCT, including 1) IFN-γ/DLI for relapsed disease after haploidentical alloSCT; 2) pre-emptive post-alloSCT treatment of patients transplanted with measurable residual disease (MRD) or with poor-risk AML/MDS, such as disease with TP53 mutations; and 3) prevention of relapse in patients who can only tolerate reduced-intensity conditioning regimens, which in most studies are associated with higher rates of post-alloSCT AML/MDS relapse than intensive conditioning regimens. Collectively, this work may allow more patients with AML/MDS to be referred for and ultimately benefit from alloSCT.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
