Evidence map›Paper›PMID 41324785›Full record

ArticleInternational journal of hematology2026

Comparison of quantitative PCR values and antigenemia for CMV monitoring in hematopoietic cell transplant recipients.

Yasuo Mori, Kentaro Kohno, Toshiyuki Ueno, Jun Odawara, Noriaki Kawano, Koji Nagafuji, Takuya Harada, Goichi Yoshimoto, Takuro Kuriyama, Shingo Urata and 15 more

Abstract readComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2026. 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

25 authors.

Yasuo MoriDepartment of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. yasuomr@gmail.com.ORCID http://orcid.org/0000-0001-6425-1720
Kentaro KohnoDepartment of Hematology and Oncology, JCHO Kyushu Hospital, Fukuoka, Japan.
Toshiyuki UenoDepartment of Internal Medicine, Kitakyushu Municipal Medical Center, Fukuoka, Japan.
Jun OdawaraDepartment of Hematology, Imamura General Hospital, Kagoshima, Japan.
Noriaki KawanoDepartment of Internal Medicine, Miyazaki Prefectural Miyazaki Hospital, Miyazaki, Japan.
Koji NagafujiDivision of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
Takuya HaradaDepartments of Hematology, National Hospital Organization, Kyushu Medical Center, Fukuoka, Japan.
Goichi YoshimotoDepartment of Hematology, Saga-Ken Medical Centre Koseikan, Saga, Japan.
Takuro KuriyamaDepartment of Hematology, Hamanomachi Hospital, Fukuoka, Japan.
Shingo UrataDepartment of Internal Medicine, Matsuyama Red Cross Hospital, Matsuyama, Japan.
Kazushi TanimotoDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, Ehime, Japan.
Yoshikane KikushigeDepartment of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Ryosuke OgawaDepartment of Hematology and Oncology, JCHO Kyushu Hospital, Fukuoka, Japan.
Yuju OhnoDepartment of Internal Medicine, Kitakyushu Municipal Medical Center, Fukuoka, Japan.
Tomohiko KamimuraDepartment of Hematology, Harasanshin Hospital, Fukuoka, Japan.
Yoshikiyo ItoDepartment of Hematology, Imamura General Hospital, Kagoshima, Japan.
Ken TakaseDepartments of Hematology, National Hospital Organization, Kyushu Medical Center, Fukuoka, Japan.
Tetsuya EtoDepartment of Hematology, Hamanomachi Hospital, Fukuoka, Japan.
Tomoaki FujisakiDepartment of Internal Medicine, Matsuyama Red Cross Hospital, Matsuyama, Japan.
Kazuki TanimotoDepartment of Hematology, Fukuoka Red Cross Hospital, Fukuoka, Japan.
Yuta KatayamaDepartment of Hematology, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, Hiroshima, Japan.
Koichi AkashiDepartment of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Katsuto TakenakaDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, Ehime, Japan.
Toshihiro MiyamotoDepartment of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Fukuoka BMT Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytomegalovirus (CMV) reactivation remains a major complication after hematopoietic cell transplantation (HCT), particularly in high-risk settings. Although the antigenemia (AG) assay has long been the standard CMV monitoring tool in Japan, quantitative PCR (qPCR) offers improved sensitivity and is now widely adopted. We analyzed a total of 1878 samples from 231 HCT recipients who underwent CMV monitoring at multiple centers. We evaluated the correlation between AG and qPCR results, determined qPCR thresholds equivalent to AG positivity, and compared actual AG-guided therapy durations with simulated qPCR-guided therapy. Among 1878 sample sets, AG and qPCR showed strong correlation (r = 0.65) and high concordance (87.6%). Median qPCR values increased with AG positivity level. ROC analysis identified qPCR cut-offs corresponding to 2 and 10 AG-positive cells as 99.5 and 815 IU/mL, respectively. Of 57 qPCR-only episodes, 32 resolved without AG conversion; higher qPCR levels were associated with treatment need. Simulated qPCR-guided therapy durations closely matched AG-guided therapy (median 4 weeks), but some cases required longer treatment. qPCR-based CMV monitoring is concordant with AG and feasible for preemptive therapy. Careful interpretation of low-level viremia is warranted to avoid overtreatment. Further data are needed to refine qPCR thresholds in transplant settings.

Indexed as

Antigens, ViralCytomegalovirusCytomegalovirus InfectionsHematopoietic Stem Cell TransplantationReal-Time Polymerase Chain ReactionAdolescentAdultAgedFemaleHumansMaleMiddle AgedTransplant RecipientsAntigens, ViralAntigenemiaCytomegalovirusHematopoietic cell transplantationPreemptive therapyQuantitative PCR

Identifiers

What OpenQuestion holds

Textmetadata
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.