Evidence map›Paper›PMID 33297669›Full record

ArticleHaematologica2022

Phenogenomic heterogeneity of post-transplant plasmablastic lymphomas.

Rebecca J Leeman-Neill, Craig R Soderquist, Francesca Montanari, Patricia Raciti, David Park, Dejan Radeski, Mahesh M Mansukhani, Vundavalli V Murty, Susan Hsiao, Bachir Alobeid and 1 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 23 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

11 authors at 5 institutions in 3 countries.

Rebecca J Leeman-NeillDivision of Hematopathology. rjl2165@cumc.columbia.edu.
Craig R SoderquistDivision of Hematopathology; Division of Personalized Genomic Medicine.
Francesca MontanariDivision of Hematology/Oncology, Columbia University Irving Medical Center, NY Presbyterian Hospital, New York, NY.
Patricia RacitiDepartment of Pathology, Greenwich Hospital, Greenwich, CT.
David ParkDivision of Hematopathology.
Dejan RadeskiDepartment of Haematology, Sir Charles Gairdner Hospital, Perth.
Mahesh M MansukhaniDivision of Personalized Genomic Medicine.
Vundavalli V MurtyDepartment of Medicine, Division of Cytogenetics, Columbia University Irving Medical Center, NY Presbyterian Hospital, New York, NY.
Susan HsiaoDivision of Personalized Genomic Medicine.
Bachir AlobeidDivision of Hematopathology.
Govind BhagatDivision of Hematopathology. gb96@cumc.columbia.edu.
Center for Genomic Science · ITColumbia University · USGreenwich Hospital · USPresbyterian Hospital · USSir Charles Gairdner Hospital · AU

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Plasmablastic lymphoma (PBL) is a rare and clinically aggressive neoplasm that typically occurs in immunocompromised individuals, including those with HIV infection and solid organ allograft recipients. Most prior studies have focused on delineating the clinicopathologic features and genetic attributes of HIV-related PBLs, where MYC deregulation and EBV infection, and more recently, mutations in JAK/STAT, MAP kinase, and NOTCH pathway genes have been implicated in disease pathogenesis. The phenotypic spectrum of post-transplant (PT)-PBLs is not well characterized and data on underlying genetic alterations are limited. Hence, we performed comprehensive histopathologic and immunophenotypic evaluation and targeted sequencing of 18 samples from 11 patients (8 males, 3 females, age range 12-76 years) with PT-PBL; 8 de novo and 3 preceded by other types of PTLDs. PT-PBLs displayed morphologic and immunophenotypic heterogeneity and some features overlapped those of plasmablastic myeloma. Six (55%) cases were EBV+ and 5 (45%) showed MYC rearrangement by fluorescence in situ hybridization. Recurrent mutations in epigenetic regulators (KMT2/MLL family, TET2) and DNA damage repair and response (TP53, mismatch repair genes, FANCA, ATRX), MAP kinase (KRAS, NRAS, HRAS, BRAF), JAK/STAT (STAT3, STAT6, SOCS1), NOTCH (NOTCH1, NOTCH3, SPEN), and immune surveillance (FAS, CD58) pathway genes were observed, with EBV+ and EBV- cases exhibiting similarities and differences in their mutational profiles. Clinical outcomes also varied, with survival ranging from 0-15.9 years postdiagnosis. Besides uncovering the biological heterogeneity of PT-PBL, our study highlights similarities and distinctions between PT-PBLs and PBLs occurring in other settings and reveals potentially targetable oncogenic pathways in disease subsets.

Indexed as

Epstein-Barr Virus InfectionsHIV InfectionsPlasmablastic LymphomaAdolescentAdultAgedChildFemaleHumansImmunophenotypingIn Situ Hybridization, FluorescenceMaleMiddle AgedYoung Adult

Identifiers

PMID33297669
PMCPMC8719101
OpenAlexW3110539843

What OpenQuestion holds

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LicenceCC BY-NC
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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.