Evidence map›Paper›PMID 26265183›Full record

ReviewLeukemia2015

Defining and treating high-risk multiple myeloma.

S Z Usmani, P Rodriguez-Otero, M Bhutani, M-V Mateos, J S Miguel

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05849610 (An Open Label, Multicenter, Phase 2, Pilot Study, Evaluating Early Treatment With Bispecific T-cell Redirectors), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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.

NCT05849610 phase2active not recruitingnot on this mapstarted 2023, after this paper: background citation

An Open Label, Multicenter, Phase 2, Pilot Study, Evaluating Early Treatment With Bispecific T-cell Redirectors (Teclistamab and Talquetamab) in the Frontline Therapy of Newly Diagnosed High-risk Multiple Myeloma

TypeinterventionalSponsorPETHEMA FoundationRan2023 to 2029Enrolled30ConditionsHigh-Risk de Novo Multiple MyelomaArmsDaratumumab, Bortezomib, Lenalidomide, Teclistamab, Talquetamab
3 · Its place in the literature

Who cites it

45 citing papers in PubMed.

  1. Trial
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  4. Trial
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Cellular therapy for multiple myeloma: what's now and what's next.Hematology. American Society of Hematology. Education Program · 2022
    Review
  13. Article
  14. Article
  15. The Role of DNA Repair in Genomic Instability of Multiple Myeloma.International journal of molecular sciences · 2022
    Review
  16. Article
  17. Article
  18. Case series: MRD negativity assessment usingTherapeutic advances in hematology · 2021
    Article
  19. Article
  20. 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.

S Z UsmaniDepartment of Hematologic Oncology, Blood Disorders and Bone Marrow Transplantation, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
P Rodriguez-OteroDepartment of Hematology, Clínica Universidad de Navarra, CIMA, IDISNA, Navarra, Spain.
M BhutaniDepartment of Hematologic Oncology, Blood Disorders and Bone Marrow Transplantation, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
M-V MateosDepartment of Hematology, University hospital of Salamanca, IBSAL, Salamanca, Spain.
J S MiguelDepartment of Hematology, Clínica Universidad de Navarra, CIMA, IDISNA, Navarra, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is more recently being recognized as a heterogeneous group of disease with variability in outcomes based on specific clinical and biologic predictors. MM patients can be broadly categorized into standard, intermediate and high risk for disease relapse, morbidity and mortality. The high-risk features include patient-specific factors such as old age, poor performance status and comorbidities; clinical features such as primary plasma cell leukemia and extramedullary disease; disease-specific biologic features such as deletion 17p, t(4;14) and high-risk gene expression profiling signatures. The current paper reviews the available data on best therapeutic approaches for high-risk MM.

Indexed as

Chromosome AberrationsGene Expression ProfilingHematopoietic Stem Cell TransplantationHumansMultiple Myeloma

Identifiers

PMID26265183

What OpenQuestion holds

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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.