Evidence map›Paper›PMID 40432636›Full record

ArticleCureus2025

Bioequivalent Letermovir Usage for Prophylaxis in Haploidentical Stem Cell Transplantation at High Risk of CMV Reactivation: A Report of Two Cases From India.

Arijit Nag, Baalamurugan Kt, Jeevan Kumar, Shouriyo Ghosh, Dibakar Podder, Debranjani Chattopadhyay, Saswata Saha, Rizwan Javed, Soumyadip Chatterji, Asish Rath and 2 more

Abstract readCase Reports
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Arijit NagDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Baalamurugan KtDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Jeevan KumarDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Shouriyo GhoshDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Dibakar PodderDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Debranjani ChattopadhyayDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Saswata SahaDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Rizwan JavedDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Soumyadip ChatterjiDepartment of Infectious Diseases, Tata Medical Center, Kolkata, IND.
Asish RathDepartment of Lab Hematology, Tata Medical Center, Kolkata, IND.
Reena NairDepartment of Clinical Hematology and Cellular Therapies, Tata Medical Center, Kolkata, IND.
Suyash BharatDepartment of Medical Affair, Zydus Lifesciences Ltd, Ahmedabad, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

classical hodgkin lymphomacmv prophylaxishaploidentical sctletermovirwiskott-aldrich syndrome

Identifiers

PMID40432636
PMCPMC12106792

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.