Evidence map›Paper›PMID 32572523›Full record

ArticleAnnals of hematology2020

Risk factors and associations with clinical outcomes of cytomegalovirus reactivation after haploidentical versus matched-sibling unmanipulated PBSCT in patients with hematologic malignancies.

Xiao-Ning Gao, Ji Lin, Li-Jun Wang, Fei Li, Hong-Hua Li, Shu-Hong Wang, Wen-Rong Huang, Chun-Ji Gao, Li Yu, Dai-Hong Liu

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In one paragraph

Article in Annals of hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% of its field
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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Xiao-Ning GaoDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Ji LinInstitute of Basic Medicine, Graduate School, Chinese PLA General Hospital, Beijing, 100853, China.
Li-Jun WangDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Fei LiDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Hong-Hua LiDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Shu-Hong WangDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Wen-Rong HuangDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Chun-Ji GaoDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Li YuDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China.
Dai-Hong LiuDepartment of Hematology, Chinese PLA General Hospital, Beijing, 100853, China. daihongrm@163.com.ORCID http://orcid.org/0000-0003-3334-9113
Chinese PLA General Hospital · CN

Funding

National Natural Science Foundation of China 81670135National Natural Science Foundation of China 81770203National Natural Science Foundation of China 81870109Natural Science Foundation of Beijing Municipality 7162174Natural Science Foundation of Beijing Municipality 7202191
6 · The paper itself

Abstract

In allogeneic hematopoietic stem cell transplantation recipients, cytomegalovirus (CMV) infection can cause overt CMV-associated disease, which is a main cause of transplantation-associated mortality. CMV infection correlates closely with donor's type. We therefore examined whether risk factors of CMV reactivation and clinical endpoints in patients with hematologic malignancies after allogeneic peripheral blood stem cell transplantation (PBSCT) differed between using matched-sibling donors (MSD-SCT) and haploidentical donors (HID-SCT). In this retrospective cohort study, we enrolled in 200 consecutive patients received an unmanipulated G-CSF-mobilized allogeneic PBSCT. Ninety (45%) patients received MSD-SCT and 110 (55%) received HID-SCT. Quantitative PCR was used for monitoring of CMV reactivation after transplantation. One-year cumulative incidence of CMV DNAemia was 55.0%, ranging from 23.5% in MSD-SCT group to 81.0% in HID-SCT group (p < 0.001). Although univariate analyses showed that non-myeloid malignancies, disease in complete remission status at transplantation, pretreatment with antithymocyte globulin, HLA-haploidentical donors, male donors, previous Epstein-Barr virus DNAemia, and absolute lymphocyte count on day 30 < 0.6 × 10

Indexed as

Hematologic NeoplasmsPeripheral Blood Stem Cell TransplantationSiblingsVirus ActivationAdolescentAdultAllograftsChildCytomegalovirusCytomegalovirus InfectionsDisease-Free SurvivalFemaleHumansMaleMiddle AgedRetrospective StudiesAllogeneic peripheral blood stem cell transplantationCytomegalovirusHaploidenticalMatched sibling

Identifiers

PMID32572523
OpenAlexW3036991015

What OpenQuestion holds

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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.