Evidence map›Paper›PMID 39543667›Full record

ReviewMolecular cytogenetics2024

Precision oncology platforms: practical strategies for genomic database utilization in cancer treatment.

Antonia A Gazola, William Lautert-Dutra, Leticia Frohlich Archangelo, Rodolfo B Dos Reis, Jeremy A Squire

Abstract readReview
In one paragraph

Review in Molecular cytogenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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.

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

12 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

5 authors.

Antonia A GazolaSchool of Medicine, Pontifical Catholic University of Rio Grande do Sul - PUCRS, Av. Ipiranga, 668, Porto Alegre, RS, 90619-900, Brazil.
William Lautert-DutraDepartment of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo - USP, Ribeirao Preto, SP, 14049-900, Brazil.
Leticia Frohlich ArchangeloDepartment of Cellular and Molecular Biology and Pathogenic Bioagents, Medical School of Ribeirao Preto, University of Sao Paulo (FMRP-USP), Ribeirao Preto, SP, 14049-900, Brazil.
Rodolfo B Dos ReisDivision of Urology, Department of Surgery and Anatomy, Medical School of Ribeirao Preto, University of Sao Paulo - USP, Ribeirao Preto, SP, 14049-900, Brazil.
Jeremy A SquireDepartment of Genetics, Medical School of Ribeirao Preto, University of Sao Paulo - USP, Ribeirao Preto, SP, 14049-900, Brazil. squirej@fmrp.usp.br.

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/15011-4Fundação de Amparo à Pesquisa do Estado de São Paulo,Brazil 2021/12271-5Wellcome Trust
6 · The paper itself

Abstract

In recent years, the expansion of molecularly targeted cancer therapies has significantly advanced precision oncology. Parallel developments in next-generation sequencing (NGS) technologies have also improved precision oncology applications, making genomic analysis of tumors more affordable and accessible. Targeted NGS panels now enable the rapid identification of diverse actionable mutations, requiring clinicians to efficiently assess the predictive value of cancer biomarkers for specific treatments. The urgency for timely and accurate decision-making in oncology emphasizes the importance of reliable precision oncology software. Online clinical decision-making tools and associated cancer databases have been designed by consolidating genomic data into standardized, accessible formats. These new platforms are highly integrated and crucial for identifying actionable somatic genomic biomarkers essential for tumor survival, determining corresponding drug targets, and selecting appropriate treatments based on the mutational profile of each patient's tumor. To help oncologists and translational cancer researchers unfamiliar with these tools, we review the utility, accuracy, and comprehensiveness of several commonly used precision medicine software options currently available. Our analysis categorized selected genomic databases based on their primary content, utility, and how well they provide practical guidance for interpreting somatic biomarker data. We identified several comprehensive, mostly open-access platforms that are easy to use for genetic biomarker searches, each with unique features and limitations. Among the precision oncology tools we evaluated, we found MyCancerGenome and OncoKB to be the first choice, offering comprehensive, accurate up-to-date information on the clinical significance of somatic mutations. To illustrate the application of these precision oncology tools in clinical settings, we evaluated three case studies to see how use of the platforms could have influenced treatment planning. Most of the precision oncology software evaluated could be easily streamlined into clinical workflows to provide updated information on approved drugs and clinical trials related the actionable mutations detected. Some platforms were very intuitive and easy to use, while others, often developed in smaller academic settings, were more difficult to navigate and may not be updated consistently. Future enhancements, incorporating artificial intelligence algorithms, are likely to improve integration of the platforms with diverse big data sources, enabling more accurate predictions of potential therapeutic responses.

Indexed as

Actionable mutationsArtificial intelligenceBig data integrationCancer biomarkersChemotherapyDNA mutational analysisOncogenesOncology softwarePersonalized cancer treatmentTumor suppressor genes

Identifiers

PMID39543667
PMCPMC11566986

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.