Evidence map›Paper›PMID 34012133›Full record

ReviewLeukemia2021

The mutagenic impact of melphalan in multiple myeloma.

Francesco Maura, Niels Weinhold, Benjamin Diamond, Dickran Kazandjian, Leo Rasche, Gareth Morgan, Ola Landgren

Abstract readReview
PubMed Publisher
In one paragraph

Review in Leukemia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

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  12. Rising Prevalence of Low-FrequencyCurrent issues in molecular biology · 2024
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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

7 authors at 6 institutions in 2 countries.

Francesco Maura *Myeloma Program, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA. fxm557@med.miami.edu.ORCID http://orcid.org/0000-0002-5017-1620
Niels Weinhold *Department of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany.
Benjamin DiamondMyeloma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-8638-9365
Dickran KazandjianMyeloma Program, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA.
Leo RascheDepartment of Internal Medicine II, Division of Oncology and Hematology, Würzburg University Hospital, Würzburg, Germany.ORCID http://orcid.org/0000-0002-9536-9649
Gareth MorganPerlmutter Cancer Center, New York University Langone Health, New York, NY, USA.ORCID http://orcid.org/0000-0002-4271-6360
Ola LandgrenMyeloma Program, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA. col15@miami.edu.ORCID http://orcid.org/0000-0001-6485-4839
University of Miami · USGerman Cancer Research Center · DEMemorial Sloan Kettering Cancer Center · USNational Institutes of Health · USNYU Langone Health · USUniversitätsklinikum Würzburg · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI George S. Grills · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

The introduction of whole genome and exome sequencing partnered with advanced bioinformatic pipelines has allowed the comprehensive characterization of mutational processes (i.e., mutational signatures) in individual cancer patients. Studies focusing on multiple myeloma have defined several mutational processes, including a recently identified mutational signature (called "SBS-MM1") directly caused by exposure to high-dose melphalan (i.e., autologous stem cell transplant). High-dose melphalan exposure increases both the overall and nonsynonymous mutational burden detected between diagnosis and relapse by ~10-20%. Nevertheless, most of these mutations are acquired within the heterochromatin and late-replicating regions, rarely involving key myeloma driver genes. In this review, we summarize key studies that made this discovery possible, and we discuss potential clinical implications.

Indexed as

MutagenesisMutationHumansMelphalanMultiple MyelomaMutagensNeoplasm ProteinsMelphalanMutagensNeoplasm Proteins

Identifiers

PMID34012133
OpenAlexW3163115321

What OpenQuestion holds

Textmetadata
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.