Evidence map›Paper›PMID 28937974›Full record

Trial reportBlood cancer journal2017

High somatic mutation and neoantigen burden are correlated with decreased progression-free survival in multiple myeloma.

A Miller, Y Asmann, L Cattaneo, E Braggio, J Keats, D Auclair, S Lonial, MMRF CoMMpass Network, S J Russell, A K Stewart

Registry-linked trialOpen access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Blood cancer journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01454297 (A Prospective, Longitudinal, Observational Study in Newly Diagnosed Multiple Myeloma), which is not on this map. Cited by 105 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% 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.

NCT01454297 completednot on this map

A Prospective, Longitudinal, Observational Study in Newly Diagnosed Multiple Myeloma (MM) Patients to Assess the Relationship Between Patient Outcomes, Treatment Regimens and Molecular Profiles

TypeobservationalSponsorMultiple Myeloma Research FoundationRan2011 to 2023Enrolled1,154ConditionsMultiple Myeloma
3 · Its place in the literature

Who cites it

105 citing papers in PubMed, 1 synthesis or guideline pooled it, 148 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Review
  8. Elucidating DNA Damage-Dependent Immune System Activation.International journal of molecular sciences · 2025
    Review
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45 more citing papers are in PubMed but not listed here.

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

10 authors at 6 institutions in 1 country.

A MillerDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Y AsmannDivision of Biomedical Informatics, Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL, USA.
L CattaneoCenter for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
E BraggioDivision of Hematology and Oncology, Mayo Clinic, Scottsdale, AZ, USA.
J KeatsTranslational Genomics Research Institute, Phoenix, AZ, USA.
D AuclairMultiple Myeloma Research Foundation, Norwalk CT, USA.
S LonialDepartment of Hematology and Medical Oncology, Emory University, Atlanta, GA, USA.
MMRF CoMMpass Network
S J RussellDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
A K StewartCenter for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic · USMayo Clinic in Arizona · USEmory University · USMayo Clinic in Florida · USMultiple Myeloma Research Foundation · USTranslational Genomics Research Institute · US

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
The Role of Cereblon Pathways in MyelomaR01CA183968 · NCI · MAYO CLINIC ARIZONA · PI KUMAR, SHAJI KUNNATHU, STEWART, ALEXANDER KEITH · 2014 to 2018
$2.3M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA183968
6 · The paper itself

Abstract

Tumor-specific mutations can result in immunogenic neoantigens, both of which have been correlated with responsiveness to immune checkpoint inhibitors in highly mutagenic cancers. However, early results of single-agent checkpoint inhibitors in multiple myeloma (MM) have been underwhelming. Therefore, we sought to understand the relationship between mutation and neoantigen landscape of MM patients and responsiveness to therapies. Somatic mutation burden, neoantigen load, and response to therapy were determined using interim data from the MMRF CoMMpass study (NCT01454297) on 664 MM patients. In this population, the mean somatic and missense mutation loads were 405.84(s=608.55) and 63.90(s=95.88) mutations per patient, respectively. There was a positive linear relationship between mutation and neoantigen burdens (R

Indexed as

Mutation, MissenseAdultAgedAged, 80 and overAntigens, NeoplasmDisease-Free SurvivalFemaleHumansMaleMiddle AgedMultiple MyelomaSurvival RateAntigens, Neoplasm

Identifiers

PMID28937974
PMCPMC5709757
OpenAlexW2760556503

What OpenQuestion holds

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Registered trials

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.