Evidence map›Paper›PMID 32118627›Full record

ArticleThe American journal of surgical pathology2020

Genetic Basis of Extramedullary Plasmablastic Transformation of Multiple Myeloma.

Ying Liu, Fatima Jelloul, Yanming Zhang, Tapan Bhavsar, Caleb Ho, Mamta Rao, Natasha E Lewis, Robert Cimera, Jeeyeon Baik, Allison Sigler and 6 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of surgical pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Inflammatory gene expression profile of oral plasmablastic lymphoma.Virchows Archiv : an international journal of pathology · 2026
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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

16 authors at 2 institutions in 1 country.

Ying LiuDepartment of Pathology, Hematopathology Service.
Fatima JelloulDepartment of Pathology, Hematopathology Service.
Yanming ZhangDepartment of Pathology, Cytogenetic Laboratory.
Tapan BhavsarDepartment of Pathology, Wayne State University School of Medicine, Detroit Receiving Hospital, Detroit, MI.
Caleb HoDepartment of Pathology, Hematopathology Service.
Mamta RaoDepartment of Pathology, Cytogenetic Laboratory.
Natasha E LewisDepartment of Pathology, Hematopathology Service.
Robert CimeraDepartment of Pathology, Cytogenetic Laboratory.
Jeeyeon BaikDepartment of Pathology, Hematopathology Service.
Allison SiglerDepartment of Pathology, Hematopathology Service.
Filiz SenDepartment of Pathology, Hematopathology Service.
Mariko YabeDepartment of Pathology, Hematopathology Service.
Mikhail RoshalDepartment of Pathology, Hematopathology Service.
Ola LandgrenDepartment of Medicine, Myeloma Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Ahmet DoganDepartment of Pathology, Hematopathology Service.
Wenbin XiaoDepartment of Pathology, Hematopathology Service.
Memorial Sloan Kettering Cancer Center · USWayne State University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Translating Stress Response Targeted Therapy for B-Cell LymphomasP50CA192937 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI DALLA-FAVERA, RICCARDO, ZELENETZ, ANDREW D. · 2016 to 2020
$10.9M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA192937
6 · The paper itself

Abstract

In patients with multiple myeloma, plasmablastic transformation in the bone marrow is rare and associated with poor outcomes. The significance of discordant extramedullary plasmablastic transformation in patients with small, mature clonal plasma cells in the bone marrow has not been well studied. Here, we report the clinicopathologic, cytogenetic, and molecular features of 10 such patients (male/female: 6/4, median age: 65 y, range: 48 to 76 y) with an established diagnosis of multiple myeloma in the bone marrow composed of small, mature plasma cells in parallel with a concurrent or subsequent extramedullary plasmablastic transformation. Eight patients with available survival data showed an overall aggressive clinical course with a median survival of 4.5 months after the diagnosis of extramedullary plasmablastic transformation, despite aggressive treatment and even in patients with low-level bone marrow involvement. Pathologically, the extramedullary plasmablastic myeloma were clonally related to the corresponding bone marrow plasma cells, showed high levels of CMYC and/or P53 expression with a high Ki-67 proliferation index by immunohistochemistry and harbored more complex genomic aberrations including frequent mutations in the RAS pathway and MYC rearrangements compared with their bone marrow counterparts. In summary, although genetic and immunohistochemical studies were not uniformly performed on all cases due to the retrospective nature of this study, our data suggest that discordant extramedullary plasmablastic transformation of multiple myeloma has an aggressive clinical course and is characterized by frequent mutations in the RAS pathway and more complex genomic abnormalities.

Indexed as

AgedFemaleHumansMaleMiddle AgedMultiple MyelomaPlasma Cells

Identifiers

PMID32118627
PMCPMC7225029
OpenAlexW3009071170

What OpenQuestion holds

Textmetadata
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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.