Evidence map›Paper›PMID 35753868›Full record

ReviewBlood reviews2022

Game of clones: Diverse implications for clonal hematopoiesis in lymphoma and multiple myeloma.

Jeremy Meier, Jeffrey L Jensen, Christopher Dittus, Catherine C Coombs, Samuel Rubinstein

Abstract readReview
In one paragraph

Review in Blood reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
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

5 authors at 1 institution in 1 country.

Jeremy MeierDepartment of Medicine, Division of Hematology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
Jeffrey L JensenDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
Christopher DittusDepartment of Medicine, Division of Hematology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
Catherine C CoombsDepartment of Medicine, Division of Hematology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America. Electronic address: calliecoombs@gmail.com.
Samuel RubinsteinDepartment of Medicine, Division of Hematology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.
University of North Carolina at Chapel Hill · US

Funding

Duke-UNC Chapel Hill Immunotherapy Training GrantT32CA211056 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHAO, NELSON J., SERODY, JONATHAN S. · 2017 to 2021
$2.2M
Institutional Clinical and Translational Science Award (UW-Madison)(TL1)TL1RR025013 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$1.1M
UNC Immunotherapy Training Grant (IM-TAG)T32CA285257 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Jonathan S. Serody · 2023 to 2026
$668k
NCI NIH HHS T32 CA211056NCI NIH HHS T32 CA285257NCRR NIH HHS TL1 RR025013
6 · The paper itself

Abstract

Clonal hematopoiesis (CH) refers to the disproportionate expansion of hematopoietic stem cell clones and their corresponding progeny following the acquisition of somatic mutations. CH is common at the time of diagnosis in patients with blood cancers, including multiple myeloma (MM) and lymphoma. The presence of CH mutations correlates with IL-6 mediated inflammation and may result in lymphoma or MM modulation through microenvironment effects or by manifestations of the mutations themselves within the founding tumor clone. As might be expected with a variety of mutations and multiple potential mechanisms, CH exerts context-dependent effects, being protective in some settings and harmful in others. Though CH is very common in patients with hematologic malignancies, how it intersects with therapy and the natural disease course of these cancers are active areas of investigation. In lymphomas and MM specifically, patients have high rates of CH at diagnosis and are subsequently exposed to therapies, such as cytotoxic chemotherapy, that can cause CH progression to overt hematologic malignancy. The expanding diversity of treatment modalities for these cancers also increases the opportunities for CH to impact clinical outcome and modulate clinical responses. Here we review the basic biology and known health effects of CH, and we focus on the clinical relevance of CH in lymphoma and MM.

Indexed as

Hematologic NeoplasmsLymphomaMultiple MyelomaClonal HematopoiesisClone CellsHematopoiesisHumansInterleukin-6MutationTumor MicroenvironmentInterleukin-6Autologous stem cell transplantCHIPClonal hematopoiesisLymphomaMultiple myeloma

Identifiers

PMID35753868
PMCPMC12606726
OpenAlexW4283389606

What OpenQuestion holds

Textmetadata
LicenceTDM
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.