ArticleCureus2025
Bioequivalent Letermovir Usage for Prophylaxis in Haploidentical Stem Cell Transplantation at High Risk of CMV Reactivation: A Report of Two Cases From India.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cytomegalovirus (CMV) reactivation is a major complication in allogeneic hematopoietic stem cell transplantation (HSCT), increasing nonrelapse mortality (NRM) and transplant-related complications. Letermovir, a CMV deoxyribonucleic acid (DNA) terminase inhibitor, has demonstrated efficacy in reducing CMV reactivation without the hematologic toxicity associated with traditional antivirals. We report two HSCT cases, one with a T-cell receptor (TCR) alpha/beta-depleted haploidentical transplant and another haploidentical (6/10 HLA-matched) stem cell transplant, both at significant risk for CMV reactivation. Letermovir prophylaxis was initiated early post-transplant and continued for 100-200 days, depending on risk factors. Both patients remained free of CMV reactivation throughout follow-up (beyond Day +140), with no breakthrough CMV infection or drug-related adverse effects. This case series highlights the first real-world use of letermovir, India's bioequivalent letermovir, in haploidentical transplant recipients, supporting its clinical effectiveness in a resource-limited setting. Real-world outcomes were consistent with previously reported clinical trial data. While outcomes were favorable, the small sample size and single-center experience represent limitations. Nonetheless, the findings highlight the potential benefit of extended prophylaxis beyond Day 100 and the need for individualized CMV prevention strategies in immunosuppressed populations.
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