Evidence map›Paper›PMID 34775986›Full record

ArticleInfectious agents and cancer2021

Metagenomic analysis to identify novel infectious agents in systemic anaplastic large cell lymphoma.

Parag Mahale, Jason Nomburg, Joo Y Song, Mia Steinberg, Gabriel Starrett, Joseph Boland, Charles F Lynch, Amy Chadburn, Paul G Rubinstein, Brenda Y Hernandez and 3 more

Open access · goldAbstract read
In one paragraph

Article in Infectious agents and cancer, 2021. 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
0.1field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

13 authors at 8 institutions in 1 country.

Parag Mahale *Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA.
Jason Nomburg *Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Joo Y SongDepartment of Pathology, City of Hope National Medical Center, Duarte, CA, USA.
Mia SteinbergCancer Genomics Research Laboratory, National Cancer Institute, Rockville, MD, USA.
Gabriel StarrettLaboratory of Cellular Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Joseph BolandCancer Genomics Research Laboratory, National Cancer Institute, Rockville, MD, USA.
Charles F LynchDepartment of Epidemiology, The University of Iowa College of Public Health, Iowa City, Iowa, USA.
Amy ChadburnPathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA.
Paul G RubinsteinStroger Hospital of Cook County, Ruth M. Rothstein Core Center, Rush University Medical Center, Chicago, IL, USA.
Brenda Y HernandezUniversity of Hawaii Cancer Center, Honolulu, HI, USA.
Dennis D WeisenburgerDepartment of Pathology, City of Hope National Medical Center, Duarte, CA, USA.
Susan BullmanHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Eric A EngelsInfections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD, USA. engelse@exchange.nih.gov.ORCID http://orcid.org/0000-0003-0203-6958
National Cancer Institute · USCity Of Hope National Medical Center · USCornell University · USFred Hutch Cancer Center · USHarvard University · USRush University Medical Center · USUniversity of Hawaiʻi at Mānoa · USUniversity of Iowa · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Systemic anaplastic large cell lymphoma (ALCL) is a rare CD30-expressing T-cell non-Hodgkin lymphoma. Risk of systemic ALCL is highly increased among immunosuppressed individuals. Because risk of cancers associated with viruses is increased with immunosuppression, we conducted a metagenomic analysis of systemic ALCL to determine whether a known or novel pathogen is associated with this malignancy. Total RNA was extracted and sequenced from formalin-fixed paraffin-embedded tumor specimens from 19 systemic ALCL cases (including one case from an immunosuppressed individual with human immunodeficiency virus infection), 3 Epstein-Barr virus positive diffuse large B-cell lymphomas (DLBCLs) occurring in solid organ transplant recipients (positive controls), and 3 breast cancers (negative controls). We used a pipeline based on the Genome Analysis Toolkit (GATK)-PathSeq algorithm to subtract out human RNA reads and map the remaining RNA reads to microbes. No microbial association with ALCL was identified, but we found Epstein-Barr virus in the DLBCL positive controls and determined the breast cancers to be negative. In conclusion, we did not find a pathogen associated with systemic ALCL, but because we analyzed only one ALCL tumor from an immunosuppressed person, we cannot exclude the possibility that a pathogen is associated with some cases that arise in the setting of immunosuppression.

Indexed as

ImmunosuppressionLymphomaMetagenomicsViruses

Identifiers

PMID34775986
PMCPMC8591940
OpenAlexW3211902804

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.