Evidence map›Paper›PMID 42131265›Full record

ArticleNagoya journal of medical science2026

The clinical utility of metagenomic next-generation sequencing in the management of fever in patients with hematological disorders.

Jiaying Cheng, Jinle Ni, Yu Zhao, Ling Jiang, Yun Huang, Yujiao Zhang, Ping Yan, Zhiquan Long, Haipeng Fu, Xuejie Jiang

Abstract read
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Article in Nagoya journal of medical science, 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

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jiaying ChengDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Jinle NiDepartment of Hematology, Guangzhou Red Cross Hospital, Guangzhou, China.
Yu ZhaoDepartment of Hematology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
Ling JiangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yun HuangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yujiao ZhangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Ping YanDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zhiquan LongDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Haipeng FuDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Xuejie JiangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with hematological malignancies frequently present with severe and intricate infections that pose life-threatening risks. Conventional pathogen detection methods offer limited clinical insights and therapeutic guidance. This retrospective study evaluated the clinical application of metagenomic next-generation sequencing (mNGS) in hematologic patients who remained febrile despite prolonged antibiotic therapy, which means unresponsive to antibiotic therapy. This retrospective analysis included 204 patients with hematologic malignancies, undergoing conventional pathogen detection and peripheral blood mNGS. The cohort was stratified into neutropenia and non-neutropenia groups to compare the diagnostic and therapeutic implications of mNGS versus conventional microbiological tests (CMT). Among the 204 patients with mNGS, the overall positive detection rate was significantly higher than that of CMT (68.1% vs 30.9%, P<0.001). In both the neutropenia and non-neutropenia group, mNGS demonstrated a higher positivity rate for bacteria than for CMT (bacteria, 36.4% vs 15.6%, P<0.01). mNGS proved notably advantageous for bloodstream infections with clinically relevant drug-resistant strains, particularly in the neutropenia cohort (26.4% vs 12.5%, P<0.001). Using a composite reference standard, mNGS manifested sensitivity and specificity rates of 78.4% and 61.9%, respectively. Patients in the neutropenia group derived superior clinical benefit from mNGS, including higher diagnostic accuracy and treatment efficacy (diagnosis, 56.4% vs 40.6%, P=0.036; treatment, 49.3% vs 31.3%, P = 0.016). Additionally, the 30-days mortality rate was notably higher among mNGS-positive patients who tested compared to those who tested negative (17.3% vs 1.5%, P<0.001). mNGS demonstrated clinical relevance in patients with hematologic malignancy who received prolonged antibiotic treatment and holds promise in predicting patient survival prognosis.

Indexed as

FeverHematologic NeoplasmsHigh-Throughput Nucleotide SequencingMetagenomicsAdultAgedAnti-Bacterial AgentsFemaleHumansMaleMiddle AgedNeutropeniaRetrospective StudiesAnti-Bacterial Agentsclinical utilitydiagnosisinfectionmetagenomic next-generation sequencing (mNGS)

Identifiers

PMID42131265
PMCPMC13167236

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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.