Evidence map›Paper›PMID 24732597›Full record

ArticleLeukemia2014

Gene expression profile alone is inadequate in predicting complete response in multiple myeloma.

S B Amin, W-K Yip, S Minvielle, A Broyl, Y Li, B Hanlon, D Swanson, P K Shah, P Moreau, B van der Holt and 7 more

Abstract read
In one paragraph

Article in Leukemia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

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

  1. Pooled it
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  14. Leveraging RSF and PET images for prognosis of multiple myeloma at diagnosis.International journal of computer assisted radiology and surgery · 2020
    Review
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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

17 authors.

S B Amin1] Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA [2] Department of Hematology/Oncology, Boston VA Healthcare System, Harvard Medical School, Boston, MA, USA [3] Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
W-K YipDepartment of Biostatistics, Harvard School of Public Health, Boston, MA, USA.
S Minvielle1] Hematology Department, Hopital de Nantes, 9, Quai Moncousu, Nantes, France [2] Department of Hematology, Inserm U892, University of Nantes, Nantes, France.
A BroylDepartment of Hematology and HOVON Data Center, Erasmus Medical Center and University, Rotterdam, The Netherlands.
Y LiDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
B HanlonDepartment of Statistics, University of Wisconsin, Madison, WI, USA.
D SwansonDepartment of Biostatistics, Harvard School of Public Health, Boston, MA, USA.
P K Shah1] Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA [2] Department of Biostatistics, Harvard School of Public Health, Boston, MA, USA.
P Moreau1] Hematology Department, Hopital de Nantes, 9, Quai Moncousu, Nantes, France [2] Department of Hematology, Inserm U892, University of Nantes, Nantes, France.
B van der HoltDepartment of Hematology and HOVON Data Center, Erasmus Medical Center and University, Rotterdam, The Netherlands.
M van DuinDepartment of Hematology and HOVON Data Center, Erasmus Medical Center and University, Rotterdam, The Netherlands.
F Magrangeas1] Hematology Department, Hopital de Nantes, 9, Quai Moncousu, Nantes, France [2] Department of Hematology, Inserm U892, University of Nantes, Nantes, France.
P Pieter Sonneveld1] Hematology Department, Hopital de Nantes, 9, Quai Moncousu, Nantes, France [2] Department of Hematology, Inserm U892, University of Nantes, Nantes, France.
K C AndersonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
C Li1] Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA [2] Department of Biostatistics, Harvard School of Public Health, Boston, MA, USA.
H Avet-Loiseau1] Hematology Department, Hopital de Nantes, 9, Quai Moncousu, Nantes, France [2] Department of Hematology, Inserm U892, University of Nantes, Nantes, France.
N C Munshi1] Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA [2] Department of Hematology/Oncology, Boston VA Healthcare System, Harvard Medical School, Boston, MA, USA.

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
Targeting Myeloma Cell-Host Bone Marrow InteractionsP01CA078378 · NCI · DANA-FARBER CANCER INSTITUTE · PI WELLER, EDIE A · 1998 to 2014
$26.2M
dChip:Analysis and Visualization of Oligonucleotide Expression and SNP ArraysR01GM077122 · NIGMS · DANA-FARBER CANCER INST · PI LI, CHENG · 2008 to 2010
$1.1M
MOLECULAR MANIPULATION TO ENHANCE ANTI-MYELOMA RESPONSEI01BX001584 · VA · VA BOSTON HEALTH CARE SYSTEM · PI MUNSHI, NIKHIL C. · 2013 to 2025
–
BLRD VA I01 BX001584NCI NIH HHS P01 CA078378NCI NIH HHS P01 CA155258NCI NIH HHS P50 CA100707NIGMS NIH HHS R01 GM077122NIGMS NIH HHS R01GM077122PHS HHS P01-155258PHS HHS P01-78378PHS HHS P50-100007PHS HHS R01-050947PHS HHS R01-124929
6 · The paper itself

Abstract

With advent of several treatment options in multiple myeloma (MM), a selection of effective regimen has become an important issue. Use of gene expression profile (GEP) is considered an important tool in predicting outcome; however, it is unclear whether such genomic analysis alone can adequately predict therapeutic response. We evaluated the ability of GEP to predict complete response (CR) in MM. GEP from pretreatment MM cells from 136 uniformly treated MM patients with response data on an IFM, France led study were analyzed. To evaluate variability in predictive power due to microarray platform or treatment types, additional data sets from three different studies (n=511) were analyzed using same methods. We used several machine learning methods to derive a prediction model using training and test subsets of the original four data sets. Among all methods employed for GEP-based CR predictive capability, we got accuracy range of 56-78% in test data sets and no significant difference with regard to GEP platforms, treatment regimens or in newly diagnosed or relapsed patients. Importantly, permuted P-value showed no statistically significant CR predictive information in GEP data. This analysis suggests that GEP-based signature has limited power to predict CR in MM, highlighting the need to develop comprehensive predictive model using integrated genomics approach.

Indexed as

TranscriptomeGenetic TestingHumansMicroarray AnalysisMultiple MyelomaRemission InductionSecondary PreventionSensitivity and Specificity

Identifiers

PMID24732597
PMCPMC4198516

What OpenQuestion holds

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Registered trials

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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.