Evidence map›Paper›PMID 37907723›Full record

ReviewNature reviews. Clinical oncology2024

Computational immunogenomic approaches to predict response to cancer immunotherapies.

Venkateswar Addala, Felicity Newell, John V Pearson, Alec Redwood, Bruce W Robinson, Jenette Creaney, Nicola Waddell

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Clinical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 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.

Venkateswar AddalaCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia. venkateswar.addala@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0002-3569-2065
Felicity NewellCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.ORCID http://orcid.org/0000-0003-0469-2705
John V PearsonCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.ORCID http://orcid.org/0000-0003-0904-4598
Alec RedwoodNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, Western Australia, Australia.ORCID http://orcid.org/0000-0001-8601-8292
Bruce W RobinsonNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, Western Australia, Australia.
Jenette CreaneyNational Centre for Asbestos Related Diseases, University of Western Australia, Perth, Western Australia, Australia.ORCID http://orcid.org/0000-0002-9391-9395
Nicola WaddellCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia. nic.waddell@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0002-3950-2476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunogenomics is an emerging field that bridges genomics and immunology. The establishment of large-scale genomic collaborative efforts along with the development of new single-cell transcriptomic techniques and multi-omics approaches have enabled characterization of the mutational and transcriptional profiles of many cancer types and helped to identify clinically actionable alterations as well as predictive and prognostic biomarkers. Researchers have developed computational approaches and machine learning algorithms to accurately obtain clinically useful information from genomic and transcriptomic sequencing data from bulk tissue or single cells and explore tumours and their microenvironment. The rapid growth in sequencing and computational approaches has resulted in the unmet need to understand their true potential and limitations in enabling improvements in the management of patients with cancer who are receiving immunotherapies. In this Review, we describe the computational approaches currently available to analyse bulk tissue and single-cell sequencing data from cancer, stromal and immune cells, as well as how best to select the most appropriate tool to address various clinical questions and, ultimately, improve patient outcomes.

Indexed as

NeoplasmsGene Expression ProfilingGenomicsHumansImmunotherapyTranscriptomeTumor Microenvironment

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.