Evidence map›Paper›PMID 36751511›Full record

ArticleHemaSphere2023

Impact of Ultra High-risk Genetics on Real-world Outcomes of Transplant-eligible Multiple Myeloma Patients.

Aikaterini Panopoulou, Sandra Easdale, Mark Ethell, Emma Nicholson, Mike Potter, Asterios Giotas, Helena Woods, Tracy Thornton, Charlotte Pawlyn, Kevin D Boyd and 1 more

Abstract read
In one paragraph

Article in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

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

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

  1. International Myeloma Society/International Myeloma Working Group Consensus Recommendations on the Definition of High-Risk Multiple Myeloma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Guideline
  2. Article
  3. Article
  4. Article
  5. Recent Advances in The Definition of the Molecular Alterations Occurring in Multiple Myeloma.Mediterranean journal of hematology and infectious diseases · 2024
    Review
  6. Article
  7. 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

11 authors.

Aikaterini PanopoulouMyeloma Molecular Therapy Group, Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
Sandra EasdaleDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Mark EthellDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Emma NicholsonDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Mike PotterDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Asterios GiotasDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Helena WoodsDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Tracy ThorntonDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Charlotte PawlynMyeloma Molecular Therapy Group, Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.
Kevin D BoydDepartment of Haematology, The Royal Marsden Hospital, London, United Kingdom.
Martin F KaiserMyeloma Molecular Therapy Group, Division of Genetics and Epidemiology, The Institute of Cancer Research, London, United Kingdom.

Funding

Cancer Research UK 29957
6 · The paper itself

Abstract

Refined prediction of early relapse following standard-of-care (SoC) autologous stem cell transplant (ASCT) in newly diagnosed multiple myeloma (NDMM) could inform real-world risk-stratified post-ASCT strategies. We investigated the impact of double hit genetics (≥2 adverse markers: t(4;14), t(14;16), t(14;20), gain(1q), del(17p)) on outcome in 139 NDMM patients who underwent SoC ASCT between January 2014 and October 2019 at our center. Double hit genetics were associated with a significantly shortened progression-free survival (hazard ratio [HR] = 4.27,

Identifiers

PMID36751511
PMCPMC9894354

What OpenQuestion holds

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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.