Evidence map›Paper›PMID 41583270›Full record

ArticleCureus2025

Cytomegalovirus Lymphadenitis After Anti-CD19 Chimeric Antigen Receptor T-cell (CAR-T): An Underappreciated Etiology of Hypermetabolic Lymphadenopathy in the Post-CAR-T Setting.

Daniel Rosas, Alissa Cox, Diana Martinez, Amneh Fares, Ihsane Ouansafi, Dante Melendez, Jose Sandoval-Sus

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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Daniel RosasHematology-Oncology, Memorial Healthcare System, Pembroke Pines, USA.
Alissa CoxInfectious Disease, Memorial Healthcare System, Pembroke Pines, USA.
Diana MartinezHematology, Memorial Healthcare System, Pembroke Pines, USA.
Amneh FaresHematology-Oncology, Memorial Healthcare System, Pembroke Pines, USA.
Ihsane OuansafiHematopathology, Memorial Healthcare System, Pembroke Pines, USA.
Dante MelendezInfectious Disease, Memorial Healthcare System, Pembroke Pines, USA.
Jose Sandoval-SusHematology-Oncology, Moffitt Cancer Center, Memorial Healthcare System, Pembroke Pines, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T-cell (CAR-T) is a revolutionary type of immunotherapy that genetically engineers a patient's own immune T-cells to recognize and attack cancer cells. This type of therapy has transformed the treatment of relapsed/refractory large B-cell lymphoma (LBCL). However, profound immunosuppression may lead to opportunistic infections that could resemble relapse in rare situations. Cytomegalovirus (CMV) reactivation and clinical infection are well recognized after hematopoietic stem cell transplantation but are less studied in the post-CAR-T setting. We describe a 56-year-old woman with primary refractory stage IV diffuse LBCL, not otherwise specified, treated with axicabtagene ciloleucel. She initially achieved a complete remission (CR), but at six months s/p CAR-T, she developed constitutional symptoms and non-tender palpable lymphadenopathy. Positron emission tomography (PET) and computed tomography (CT) demonstrated hypermetabolic cervical and axillary lymph nodes, as well as focal uptake in the appendix. A biopsy did not show relapsed lymphoma but did reveal classic CMV inclusions, positive CMV immunohistochemistry, and high-level tissue CMV DNA despite negative plasma PCR, with a final diagnosis of CMV lymphadenitis. Symptoms resolved with a three-week course of valganciclovir, and follow-up imaging showed near-complete resolution of the disease. CMV lymphadenitis is a rare but important differential diagnosis of hypermetabolic lymphadenopathy in the post-CAR-T setting, which can mimic lymphoma relapse. Tissue biopsy remains essential for accurate diagnosis and to prevent unnecessary oncologic therapy. Clinicians should maintain vigilance for infectious etiologies in this setting, and future studies may clarify whether targeted CMV monitoring is warranted in high-risk patients.

Indexed as

allogeneic stem cell transplant recipientscytomegalovirus (cmv)hemato-oncologynon-hodgkin's lymphomaoncolog

Identifiers

PMID41583270
PMCPMC12830317

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Registered trials

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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.