Evidence map›Paper›PMID 33937058›Full record

ArticleFrontiers in oncology2021

Machine Learning Applicability for Classification of PAD/VCD Chemotherapy Response Using 53 Multiple Myeloma RNA Sequencing Profiles.

Nicolas Borisov, Anna Sergeeva, Maria Suntsova, Mikhail Raevskiy, Nurshat Gaifullin, Larisa Mendeleeva, Alexander Gudkov, Maria Nareiko, Andrew Garazha, Victor Tkachev and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
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

17 citing papers in PubMed, 33 citations in OpenAlex.

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  4. Construction of a treatment response prediction model for multiple myeloma based on multi-omics and machine learning.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
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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

14 authors at 6 institutions in 2 countries.

Nicolas BorisovMoscow Institute of Physics and Technology, Laboratory for Translational Genomic Bioinformatics, Dolgoprudny, Russia.
Anna SergeevaNational Research Center for Hematology, Ministry of Health of the Russian Federation, Moscow, Russia.
Maria SuntsovaI.M. Sechenov First Moscow State Medical University, Institute of Personalized Medicine, Moscow, Russia.
Mikhail RaevskiyMoscow Institute of Physics and Technology, Laboratory for Translational Genomic Bioinformatics, Dolgoprudny, Russia.
Nurshat GaifullinDepartment of Pathology, Faculty of Medicine, Lomonosov Moscow State University, Moscow, Russia.
Larisa MendeleevaNational Research Center for Hematology, Ministry of Health of the Russian Federation, Moscow, Russia.
Alexander GudkovI.M. Sechenov First Moscow State Medical University, Institute of Personalized Medicine, Moscow, Russia.
Maria NareikoNational Research Center for Hematology, Ministry of Health of the Russian Federation, Moscow, Russia.
Andrew GarazhaOmicsway Corp., Research Department, Walnut, CA, United States.
Victor TkachevOmicsway Corp., Research Department, Walnut, CA, United States.
Xinmin LiDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, CA, United States.
Maxim SorokinI.M. Sechenov First Moscow State Medical University, Institute of Personalized Medicine, Moscow, Russia.
Vadim SurinNational Research Center for Hematology, Ministry of Health of the Russian Federation, Moscow, Russia.
Anton BuzdinI.M. Sechenov First Moscow State Medical University, Institute of Personalized Medicine, Moscow, Russia.
Ministry of Health of the Russian Federation · RUInstitute of Bioorganic Chemistry · RUMoscow Institute of Physics and Technology · RUSechenov University · RULomonosov Moscow State University · RUUniversity of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
NCI NIH HHS P30 CA016042
6 · The paper itself

Abstract

Multiple myeloma (MM) affects ~500,000 people and results in ~100,000 deaths annually, being currently considered treatable but incurable. There are several MM chemotherapy treatment regimens, among which eleven include bortezomib, a proteasome-targeted drug. MM patients respond differently to bortezomib, and new prognostic biomarkers are needed to personalize treatments. However, there is a shortage of clinically annotated MM molecular data that could be used to establish novel molecular diagnostics. We report new RNA sequencing profiles for 53 MM patients annotated with responses on two similar chemotherapy regimens: bortezomib, doxorubicin, dexamethasone (PAD), and bortezomib, cyclophosphamide, dexamethasone (VCD), or with responses to their combinations. Fourteen patients received both PAD and VCD; six received only PAD, and 33 received only VCD. We compared profiles for the good and poor responders and found five genes commonly regulated here and in the previous datasets for other bortezomib regimens (all upregulated in the good responders):

Indexed as

bortezomibfibroblast growth factor receptor 3gene expressionmachine learningmultiple myelomaPADtreatment responseVCD

Identifiers

PMID33937058
PMCPMC8083158
OpenAlexW3153248834

What OpenQuestion holds

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LicenceCC BY
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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.