Evidence map›Paper›PMID 39638995›Full record

Observational studyBlood cancer journal2024

Real-world characteristics and outcomes of patients with high-risk and non-high-risk smoldering multiple myeloma using the Flatiron Health database.

S Vincent Rajkumar, María-Victoria Mateos, Marcy Schaeffer, Xiwu Lin, Sacheeta Bathija, Niodita Gupta-Werner, Annette Lam, Robin Carson, Robyn Dennis, Shuchita Kaila and 3 more

Abstract readObservational Study
In one paragraph

Observational study in Blood cancer journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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.

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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

13 authors.

S Vincent RajkumarMayo Clinic, Rochester, MN, USA.ORCID 0000-0002-5862-1833
María-Victoria MateosHospital Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Centro de Investigación del Cancer (IBMCC-USAL, CSIC), Salamanca, Spain.ORCID 0000-0003-2390-1218
Marcy SchaefferJanssen Pharmaceutica NV, Beerse, Belgium.
Xiwu LinJanssen Global Services, Horsham, PA, USA.
Sacheeta BathijaJanssen Global Services, Raritan, NJ, USA.
Niodita Gupta-WernerJanssen Scientific Affairs, Horsham, PA, USA.
Annette LamJanssen Global Services, Raritan, NJ, USA.
Robin CarsonJanssen Research & Development, Wayne, PA, USA.
Robyn DennisJanssen Research & Development, Wayne, PA, USA.
Shuchita KailaJanssen Scientific Affairs, Horsham, PA, USA.
Kathryn MattJanssen Global Services, Raritan, NJ, USA.
Joana DuranJanssen Global Services, Raritan, NJ, USA.
Sagar LonialEmory University School of Medicine, Atlanta, GA, USA. sloni01@emory.edu.ORCID 0000-0002-8322-9323

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Yi Lin · 2015 to 2026
$25.5M
NCI NIH HHS P50 CA186781
6 · The paper itself

Abstract

This study aimed to provide real-world evidence on progression risk in patients with high-risk smoldering multiple myeloma (SMM). This retrospective, observational study leveraged data from the Flatiron Health database. Eligible patients had SMM and relevant measures to apply Mayo 2018, International Myeloma Working Group (IMWG) 2020, and AQUILA trial risk criteria. Time to progression to active MM (TTP), progression or death (PFS), and death or progression on first-line MM therapy (PFS2) were evaluated using Kaplan-Meier methods and multivariate Cox regression models adjusted for age, Charlson Comorbidity Index, and time from SMM diagnosis to risk classification date. Across the three risk models (Mayo 2018, IMWG 2020, and AQUILA trial), high-risk patients with SMM had 3.0-4.0 times the risk of TTP, 2.1-3.5 times the risk of PFS, and 1.7-3.2 times the risk of PFS2 versus non-high-risk patients (p < 0.001 for all comparisons). Similar results were observed when patients with early treatment, early progression, and/or bone disease were excluded. This study demonstrates that high-risk patients with SMM have worse prognoses than non-high-risk patients, regardless of the criteria used, and highlights a need for early intervention testing.

Indexed as

Databases, FactualSmoldering Multiple MyelomaAdultAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedMultiple MyelomaRetrospective StudiesRisk Factors

Identifiers

PMID39638995
PMCPMC11621302

What OpenQuestion holds

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LicenceCC BY
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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.