Evidence map›Paper›PMID 41981081›Full record

ArticleBone marrow transplantation2026

Impact of antiviral therapies on survival in patients with HHV-6B encephalitis after cord blood transplantation: a real-world study.

Toshiki Terao, Wataru Kitamura, Takahiro Fujino, Takami Haruyama, Yuri Okazoe, Naoyuki Uchida, Masatsugu Tanaka, Atsushi Wake, Masahito Tokunaga, Keisuke Kataoka and 16 more

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Article in Bone marrow transplantation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

26 authors.

Toshiki TeraoDepartment of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan. tarao.toshiki.0127@gmail.com.ORCID 0000-0002-6728-3346
Wataru KitamuraDepartment of Hematology and Blood Transfusion, Kochi Health Sciences Center, Kochi, Japan.ORCID 0000-0002-8021-4732
Takahiro FujinoDivision of Hematology and Oncology, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID 0000-0001-7817-093X
Takami HaruyamaDepartment of Medical Oncology and Hematology, Oita University Faculty of Medicine, Yufu, Japan.
Yuri OkazoeDepartment of Medical Oncology and Hematology, Kobe University Hospital, Kobe, Japan.
Naoyuki UchidaDepartment of Hematology, Federation of National Public Service Personnel Mutual Aid Associations TORANOMON HOSPITAL, Minato-ku, Japan.ORCID 0000-0001-5952-5926
Masatsugu TanakaDepartment of Hematology, Kanagawa Cancer Center, Yokohama, Japan.
Atsushi WakeDepartment of Hematology, Federation of National Public Service Personnel Mutual Aid Associations, Toranomon Hospital, Kajigaya, Japan.ORCID 0000-0002-9653-6170
Masahito TokunagaDepartment of Hematology, Imamura General Hospital, Kagoshima, Japan.ORCID 0000-0003-1296-9006
Keisuke KataokaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Shinjuku-ku, Japan.ORCID 0009-0006-7339-9800
Masashi SawaDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Makoto OnizukaDepartment of Hematology/Oncology, Tokai University School of Medicine, Isehara, Japan.ORCID 0000-0003-3864-0823
Masako ToyosakiDepartment of Hematology/Oncology, Tokai University School of Medicine, Isehara, Japan.
Koichi OnoderaDepartment of Hematology, Tohoku University Hospital, Sendai, Japan.
Tetsuya NishidaDepartment of Hematology, Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital, Nagoya, Japan.
Yuta KatayamaDepartment of Hematology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima, Japan.ORCID 0000-0001-5054-9104
Takeshi MaedaDepartment of Hematology/Oncology, Kurashiki Central Hospital, Kurashiki, Japan.
Yuta HasegawaDepartment of Hematology, Hokkaido University Hospital, Sapporo, Japan.
Shunya AraiDepartment of Hematology, Kyorin University Hospital, Mitaka, Japan.
Makoto YoshimitsuDepartment of Hematology and Rheumatology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.ORCID 0000-0002-5935-0385
Takahiro FukudaDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tsukiji, Japan.
Marie OhbikiJapanese Data Center for Hematopoietic Cell Transplantation, Nagakute, Japan.
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagakute, Japan.ORCID 0000-0003-4404-2870
Kimikazu YakushijinDepartment of Medical Oncology and Hematology, Kobe University Hospital, Kobe, Japan.ORCID 0000-0003-2511-7857
Masao OgataDepartment of Medical Oncology and Hematology, Oita University Faculty of Medicine, Yufu, Japan.ORCID 0000-0002-4896-5878
Hideki NakasoneDivision of Emerging Medicine for Integrated Therapeutics, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Japan.ORCID 0000-0001-5812-9315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this registry-based study, we evaluated the efficacy of different antiviral therapies for adult patients who developed human herpesvirus-6B (HHV-6B) encephalitis after their first cord blood transplantation (CBT). Among 3,862 CBT recipients registered in Japan between January 2019 and December 2023, HHV-6B encephalitis occurred in 289 patients within 100 days post-transplant (7.5%). Antiviral treatments included foscarnet (FCN) monotherapy (n = 190), ganciclovir (GCV) monotherapy (n = 12), and FCN/GCV combination therapy (n = 74). The FCN/GCV group was associated with a potential improvement in 1-year survival compared with the FCN and GCV groups (63.2% vs. 52.5% vs. 41.7%, p = 0.38). Moreover, FCN/GCV therapy was identified as an independent predictor of improved survival compared with FCN monotherapy (HR, 0.60; 95% CI, 0.38-0.95; p = 0.031). Furthermore, the combination FCN/GCV therapy showed better survival than FCN monotherapy in the patients after neutrophil engraftment (1-year survival 68.1% vs. 51.6%), but worse survival in patients before engraftment (1-year survival 34.1% vs. 54.6%). Together, these findings provide real-world evidence linking antiviral regimen selection to post-transplant outcomes in HHV-6B encephalitis and suggest that FCN/GCV combination therapy may offer a survival advantage over FCN monotherapy in selected CBT patients, with treatment strategies potentially tailored according to hematologic recovery.

Indexed as

Antiviral AgentsCord Blood Stem Cell TransplantationEncephalitis, ViralHerpesvirus 6, HumanRoseolovirus InfectionsAdultFemaleGanciclovirHumansJapanMaleMiddle AgedRegistriesSurvival RateAntiviral AgentsGanciclovir

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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.