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The Use of Cytomegalovirus Cell Mediated Immunity to Optimize the Duration of Letermovir Prophylaxis in Hematopoietic Cell Transplant Recipients

RecruitingNAAges 18 Years - anyAllM.D. Anderson Cancer Center
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In plain words

What the trial is, and whether it could suit you

The goal of this laboratory research study is to learn if interrupting a patient's letermovir dosing based on their immune system response can help HSC transplant patients avoid post-treatment CMV infections better than taking letermovir every day without interruption.

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion criteria 1. Allogeneic HCT recipients with positive CMV serostatus 2. On letermovir prophylaxis at day 90 post transplant (+/- 7 days) 3. At high risk for CMV reactivation after day +100: 1. Prior or active graft versus host disease requiring systemic steroids 2. Mismatch stem cell donor (includes haploidentical, mismatch unrelated donor (MMUD), match related donor with at least one mismatch at one of the three specified HLA gene loci (HLA-A, HLA-B, or HLA-DR) and cord donor recipients) 3. Received T cell depletion or anti thymoglobulin during conditioning 4. CMV reactivation prior to day 100 post transplant 5. On steroids at any dose within 2 weeks of enrollment Exclusion criteria 1. Patients under the age of 18 2. Patients are discharged from our institution and unwilling to come back for follow up 3. Patients are actively undergoing treatment for CS-CMVi at time of screening. Prior CS-CMVi is not an exclusion from study. 4. Patients are allergic or intolerant to letermovir or have history of letermovir resistant CMV infection. 5. Not able to procure letermovir for extended prophylaxis beyond day +100.
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What it tests

  • Hematopoietic Cell Transplant
  • Letermovir
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Where

1 site
The University of Texas MD Anderson Cancer Center
Houston, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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