Evidence map›Paper›PMID 34247136›Full record

ArticleTranslational oncology2021

AI-supported modified risk staging for multiple myeloma cancer useful in real-world scenario.

Akanksha Farswan, Anubha Gupta, Ritu Gupta, Saswati Hazra, Sadaf Khan, Lalit Kumar, Atul Sharma

Abstract read
In one paragraph

Article in Translational oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

10 citing papers in PubMed.

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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

7 authors.

Akanksha FarswanSBILab, Department of ECE, Indraprastha Institute of Information Technology-Delhi, New Delhi 110020, India.
Anubha GuptaSBILab, Department of ECE, Indraprastha Institute of Information Technology-Delhi, New Delhi 110020, India. Electronic address: anubha@iiitd.ac.in.
Ritu GuptaLaboratory Oncology Unit, Dr. B.R.A. IRCH, AIIMS, New Delhi 110029, India. Electronic address: drritu.laboncology@aiims.edu.
Saswati HazraSBILab, Department of ECE, Indraprastha Institute of Information Technology-Delhi, New Delhi 110020, India.
Sadaf KhanLaboratory Oncology Unit, Dr. B.R.A. IRCH, AIIMS, New Delhi 110029, India.
Lalit KumarDepartment of Medical Oncology, Dr. B.R.A. IRCH, AIIMS, New Delhi, India.
Atul SharmaDepartment of Medical Oncology, Dr. B.R.A. IRCH, AIIMS, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAn efficient readily employable risk prognostication method is desirable for MM in settings where genomics tests cannot be performed owing to geographical/economical constraints. In this work, a new Modified Risk Staging (MRS) has been proposed for newly diagnosed Multiple Myeloma (NDMM) that exploits six easy-to-acquire clinical parameters i.e. age, albumin, β2-microglobulin (β2M), calcium, estimated glomerular filtration rate (eGFR) and hemoglobin. MATERIALS AND

methodsMRS was designed using a training cohort of 716 NDMM patients of our inhouse MM Indian (MMIn) cohort and validated on MMIn (n=354) cohort and MMRF (n=900) cohort. K-adaptive partitioning (KAP) was used to find new thresholds for the parameters. Risk staging rules, obtained via training a J48 classifier, were used to build MRS.

resultsNew thresholds were identified for albumin (3.6 g/dL), β2M (4.8 mg/L), calcium (11.13 mg/dL), eGFR (48.1 mL/min), and hemoglobin (12.3 g/dL) using KAP on the MMIn dataset. On the MMIn dataset, MRS outperformed ISS for OS prediction in terms of C-index, hazard ratios, and its corresponding p-values, but performs comparable in prediction of PFS. On both MMIn and MMRF datasets, MRS performed better than RISS in terms of C-index and p-values. A simple online tool was also designed to allow automated calculation of MRS based on the values of the parameters. DISCUSSION: Our proposed ML-derived yet simple staging system, MRS, although does not employ genetic features, outperforms RISS as confirmed by better separability in KM survival curves and higher values of C-index on both MMIn and MMRF datasets.

fundingGrant: BT/MED/30/SP11006/2015 (Department of Biotechnology, Govt. of India), Grant: DST/ICPS/CPS-Individual/2018/279(G) (Department of Science and Technology, Govt. of India), UGC-Senior Research Fellowship.

Indexed as

BIRCH clusteringHazard ratiosHematological malignancyJ48 decision treeMachine learningRisk stratification of multiple myeloma

Identifiers

PMID34247136
PMCPMC8278429

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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.