Evidence map›Paper›PMID 39160255›Full record

Observational studyNature genetics2024

Comprehensive molecular profiling of multiple myeloma identifies refined copy number and expression subtypes.

Sheri Skerget, Daniel Penaherrera, Ajai Chari, Sundar Jagannath, David S Siegel, Ravi Vij, Gregory Orloff, Andrzej Jakubowiak, Ruben Niesvizky, Darla Liles and 49 more

Erratum issued Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Nature genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT01454297 (A Prospective, Longitudinal, Observational Study in Newly Diagnosed Multiple Myeloma), which is not on this map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

73 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. iScience · 2026
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Observational
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

59 authors.

Sheri SkergetIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Daniel PenaherreraIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Ajai ChariTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.ORCID http://orcid.org/0000-0002-0405-7480
Sundar JagannathTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.ORCID http://orcid.org/0000-0003-2934-6518
David S SiegelHackensack University Medical Center, Hackensack, NJ, USA.ORCID http://orcid.org/0000-0002-3604-2574
Ravi VijDivision of Oncology, Washington University, St. Louis, MO, USA.
Gregory OrloffVirginia Cancer Specialists, Fairfax, VA, USA.
Andrzej JakubowiakUniversity of Chicago Medical Center, Chicago, IL, USA.
Ruben NiesvizkyWeill Cornell Medicine, New York City, NY, USA.
Darla LilesDivision of Hematology/Oncology, East Carolina University, Greenville, NC, USA.ORCID http://orcid.org/0000-0003-1480-7887
Jesus BerdejaSarah Cannon Research Institute, Nashville, TN, USA.ORCID http://orcid.org/0000-0003-4362-0376
Moshe LevyBaylor Scott and White Research Institute, Dallas, TX, USA.
Jeffrey WolfDepartment of Medicine, UCSF Medical Center, San Francisco, CA, USA.
Saad Z UsmaniLevine Cancer Institute, Charlotte, NC, USA.ORCID http://orcid.org/0000-0002-5484-8731
MMRF CoMMpass Network
Austin W ChristoffersonIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Sara NasserIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Jessica L AldrichIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Christophe LegendreIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Brooks BenardIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.ORCID http://orcid.org/0000-0001-7154-744X
Chase MillerIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Bryce TurnerIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Ahmet KurdogluIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Megan WashingtonIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Venkata YellapantulaIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.ORCID http://orcid.org/0000-0003-1592-7741
Jonathan R AdkinsIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Lori CuyuganIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Martin BoatengIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Adrienne HellandIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Shari KymanIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.ORCID http://orcid.org/0000-0001-5386-5866
Jackie McDonaldIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Rebecca ReimanIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Kristi StephensonIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Erica TassoneIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Alex BlanskiVan Andel Institute, Grand Rapids, MI, USA.
Brianne LivermoreVan Andel Institute, Grand Rapids, MI, USA.
Meghan KirchhoffVan Andel Institute, Grand Rapids, MI, USA.
Daniel C RohrerVan Andel Institute, Grand Rapids, MI, USA.ORCID http://orcid.org/0000-0002-1784-9196
Mattia D'AgostinoDivision of Hematology, AOU Città della Salute e della Scienza di Torino, University of Torino and Department of Molecular Biotechnology and Health Sciences, Torino, Italy.
Manuela GambellaDivision of Hematology, AOU Città della Salute e della Scienza di Torino, University of Torino and Department of Molecular Biotechnology and Health Sciences, Torino, Italy.
Kimberly CollisonSpectrum Health, Grand Rapids, MI, USA.
Jennifer StumphSpectrum Health, Grand Rapids, MI, USA.ORCID http://orcid.org/0000-0003-2423-0241
Pam KiddSpectrum Health, Grand Rapids, MI, USA.
Andrea DonnellyPrecision for Medicine, Flemington, NJ, USA.
Barbara ZauggPrecision for Medicine, Flemington, NJ, USA.
Maureen TooneInStat Services, Chatham, NJ, USA.
Kyle McBrideInStat Services, Chatham, NJ, USA.
Mary DeRomeMultiple Myeloma Research Foundation, Norwalk, CT, USA.
Jennifer RogersMultiple Myeloma Research Foundation, Norwalk, CT, USA.
David CraigIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Winnie S LiangIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.ORCID http://orcid.org/0000-0002-5698-7735
Norma C GutierrezDepartment of Hematology, University Hospital of Salamanca, IBSAL, Cancer Research Center-IBMCC (USAL-CSIC), CIBERONC, Salamanca, Spain.ORCID http://orcid.org/0000-0001-5834-9510
Scott D JewellVan Andel Institute, Grand Rapids, MI, USA.ORCID http://orcid.org/0000-0001-9469-6261
John CarptenIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Kenneth C AndersonDana-Farber Cancer Institute, Harvard Cancer Center, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6418-0886
Hearn Jay ChoTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Daniel AuclairMultiple Myeloma Research Foundation, Norwalk, CT, USA.ORCID http://orcid.org/0000-0001-5151-3058
Sagar LonialDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA. sloni01@emory.edu.
Jonathan J KeatsIntegrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA. jkeats@tgen.org.ORCID http://orcid.org/0000-0003-4375-7399

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Multiple Myeloma Research Foundation (Multiple Myeloma Research Foundation, Inc.) CoMMpass StudyNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Multiple myeloma is a treatable, but currently incurable, hematological malignancy of plasma cells characterized by diverse and complex tumor genetics for which precision medicine approaches to treatment are lacking. The Multiple Myeloma Research Foundation's Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile study ( NCT01454297 ) is a longitudinal, observational clinical study of newly diagnosed patients with multiple myeloma (n = 1,143) where tumor samples are characterized using whole-genome sequencing, whole-exome sequencing and RNA sequencing at diagnosis and progression, and clinical data are collected every 3 months. Analyses of the baseline cohort identified genes that are the target of recurrent gain-of-function and loss-of-function events. Consensus clustering identified 8 and 12 unique copy number and expression subtypes of myeloma, respectively, identifying high-risk genetic subtypes and elucidating many of the molecular underpinnings of these unique biological groups. Analysis of serial samples showed that 25.5% of patients transition to a high-risk expression subtype at progression. We observed robust expression of immunotherapy targets in this subtype, suggesting a potential therapeutic option.

Indexed as

DNA Copy Number VariationsMultiple MyelomaDisease ProgressionExome SequencingFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLongitudinal StudiesMaleMiddle AgedWhole Genome Sequencing

Identifiers

PMID39160255
PMCPMC11387199

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.