Evidence map›Paper›PMID 42164985›Full record

ReviewCurrent genomics2025

Genomics-Driven Immunotherapy: Advancing Cancer Treatment through Personalized Approaches.

Aditi A Kate, Sharav A Desai, Siddhi P Sapkal, Madhulika M More, Vipul P Patel

Abstract readReview
In one paragraph

Review in Current genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Aditi A KateDepartment of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India.
Sharav A DesaiDepartment of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India.
Siddhi P SapkalDepartment of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India.
Madhulika M MoreDepartment of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India.
Vipul P PatelDepartment of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a complex disease involving the abnormal growth and dissemination of cells. The traditional treatments of cancer suffer from challenges like drug resistance and non-specificity. However, immunotherapy has become a promising alternative, leveraging the body's immune system to attack cancer cells. However, the variability in patients' responses to immunotherapy underscores the significance of personalized treatment strategies. Genomics is key to understanding how genetic changes drive tumor development and response to immunotherapy. Genomic profiling techniques, such as NGS, enable the identification of molecular biomarkers, such as Tumor Mutational Burden (TMB) and Microsatellite Instability (MSI), that predict response to immunotherapy. Furthermore, the Tumor Microenvironment (TME), consisting of different cells and molecules surrounding the tumor, plays an important role in cancer progression and treatment outcomes. In this review, we highlight how genomics-driven approaches are accelerating cancer immunotherapy. It presents how genomics can be used to personalize immunotherapy for cancer and discusses challenges such as tumor heterogeneity and resistance to therapy, which require innovative technologies such as single-cell RNA sequencing, AI, and machine learning in immunogenomics, and liquid biopsies to refine treatment strategies. In the future, the incorporation of CRISPR-based gene editing, personalized neoantigen vaccines, and combination therapies holds great promise for transforming cancer treatment.

Indexed as

cancer immunotherapygenomic biomarkersgenomicsprecision medicineTumortumor microenvironment

Identifiers

PMID42164985
PMCPMC13154235

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.