Allied Journal of Medical Research

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.
Reach Us +1 (202) 780-3397

Mini Review - Allied Journal of Medical Research (2025) Volume 9, Issue 1

Precision Oncology: Transforming Cancer Treatment with Personalized Medicine

Walden Vaughan*

Department of Immunology, Humboldt University of Berlin, Berlin, Germany

*Corresponding Author:
Walden Vaughan
Department of Immunology
Humboldt University of Berlin, Berlin, Germany
E-mail: vwale01@yahoo.com

Received: 01-Jan-2025, Manuscript No. AAAJMR-25-161512; Editor assigned: 02-Jan-2025, Pre QC No. AAAJMR-25-161512(PQ); Reviewed:15-Jan-2025, QC No.AAAJMR-25-161512; Revised:20-Jan-2025, Manuscript No. AAAJMR-25-161512(R), Published:27-Jan-2025, DOI:10.35841/aaajmr-9.1.273

Citation: Vaughan W. Precision oncology: Transforming cancer treatment with personalized medicine. Allied J Med Res. 2025;9(1):273

Visit for more related articles at Allied Journal of Medical Research

Introduction

Cancer remains one of the most challenging diseases in modern medicine, affecting millions of people worldwide. Traditional cancer treatments, such as chemotherapy and radiation therapy, often follow a one-size-fits-all approach, which may not be effective for all patients. The advent of precision oncology has revolutionized the field by tailoring cancer treatments to the genetic and molecular profiles of individual patients. This personalized approach improves treatment efficacy, minimizes side effects, and enhances overall patient outcomes. In this article, we explore the principles of precision oncology, its technological advancements, challenges, and the future of personalized cancer treatment.Understanding Precision Oncology Precision oncology, also known as personalized cancer treatment, is an innovative approach that uses genomic and molecular data to guide therapeutic decisions. Unlike conventional treatments that target all cancer patients similarly, precision oncology identifies specific genetic mutations, biomarkers, and molecular pathways unique to each patient's tumor. By leveraging this data, oncologists can prescribe targeted therapies that directly address the underlying mechanisms driving the cancer [1,2].

The foundation of precision oncology lies in advances in genomic sequencing, particularly Next-Generation Sequencing (NGS), which enables rapid and cost-effective analysis of tumor DNA. This technology allows researchers to detect genetic abnormalities responsible for cancer progression and resistance to treatment. Additionally, Artificial Intelligence (AI) and bioinformatics play a crucial role in analyzing vast amounts of genomic data to provide precise therapeutic recommendations. Whole-genome sequencing (WGS) and Whole-Exome Sequencing (WES) help identify mutations and alterations in tumor DNA.Liquid biopsies analyze circulating tumor DNA (ctDNA) from blood samples, offering a non-invasive method for monitoring cancer progression and treatment response. [3,4].

Targeted drugs, such as Tyrosine Kinase Inhibitors (TKIs) and immune checkpoint inhibitors, attack specific molecular targets associated with cancer growth.Precision oncology has enhanced immunotherapy, enabling the development of CAR-T cell therapy, which engineers a patient’s own immune cells to fight cancer.Immune checkpoint inhibitors, such as pembrolizumab (Keytruda) and nivolumab (Opdivo), block proteins that suppress immune responses against tumors.AI-driven algorithms analyze large-scale genomic and clinical data to identify effective treatment strategies.Machine learning models predict patient responses to specific therapies, improving clinical decision-making.Genomic sequencing and targeted therapies remain expensive, limiting access for many patients, particularly in low-income regions.Insurance coverage for precision oncology treatments varies, making affordability a major concern. [5,6].

Cancers evolve over time, leading to genetic variations within the same tumor or between primary and metastatic sites. This complexity makes it difficult to identify consistent therapeutic targets. Large-scale genomic data require sophisticated bioinformatics tools for meaningful analysis. Standardizing genomic databases and improving data sharing among institutions remain ongoing challengesPersonalized treatments raise ethical concerns regarding genetic privacy and data security.Regulatory agencies, such as the FDA, face challenges in approving rapidly evolving targeted therapies. [7,8].

The future of precision oncology is bright, with ongoing research focusing on overcoming current limitations and expanding treatment options. Several promising developments include. CRISPR technology has the potential to correct cancer-causing mutations at the genetic level, opening new doors for gene therapy-based treatments.Researchers are refining liquid biopsy techniques to detect cancer at earlier stages, monitor treatment responses in real time, and prevent recurrence.Scientists are developing mRNA-based cancer vaccines tailored to individual tumor antigens, similar to COVID-19 vaccines.Combining genomics, proteomics, transcriptomics, and metabolomics data will provide a more comprehensive understanding of cancer biology and guide treatment choices more effectively. [9,10].

Conclusion

Precision oncology represents a paradigm shift in cancer treatment, offering hope for improved survival rates and better quality of life for patients. By leveraging genomic insights, targeted therapies, and innovative technologies, oncologists can develop personalized treatment plans that are more effective and less toxic than traditional approaches.

References

  1. Majunder M, Guerrini C, Bollinger J, et al. Sharing Data under the 21st Century Cures Act. Genet Med. 2017;19(12):1289–94.
  2. Indexed at, Google Scholar, Crossref

  3. Schmit C, Wetter S, Kash B. Falling short: how state laws can address health information exchange barriers and enablers. J Am Med Inform Assoc. 2018;25(06):635–44.
  4. Indexed at, Google Scholar, Crossref

  5. Nohr C, Parv L, Kink P, et al. nationwide citizen access to their health data: analyzing and comparing experiences in Denmark, Estonia and Australia. BMC Health Serv Res 201717534.
  6. Indexed at, Google Scholar, Crossref

  7. Pietro C, Francetic I. E-health in Switzerland: The laborious adoption of the federal law on electronic health records (EHR) and health information exchange (HIE) networks. Health Policy 2018;1220269–74.
  8. Indexed at, Google Scholar, Crossref

  9. Cairns J, Overbaugh J, Miller S The origin of mutants. Nature. 1988;335:142–145–249.
  10. Indexed at, Google Scholar, Crossref

  11. Hall BG Adaptive evolution that requires multiple spontaneous mutations. I. Mutations involving an insertion sequence. Genetics. 1988;120:887–897–622.
  12. Indexed at, Google Scholar, Crossref

  13. Boe L. Mechanism for induction of adaptive mutations in Escherichia coli. Molec Microbiol. 1990;4:597–601–95.
  14. Indexed at, Google Scholar, Crossref

  15. Foster PL Adaptive mutation: The uses of adversity. Annu Rev Microbiol. 1993;47:467–504–937.
  16. Indexed at, Google Scholar, Crossref

  17. Ahlquist DA, McGill DB, Schwartz S, et al Fecal blood levels in health and disease. A study using HemoQuant. N Engl J Med. 1985;312:1422–28–249.
  18. Indexed at, Google Scholar, Crossref

  19. Baker WF Jr Iron deficiency in pregnancy, obstetrics, and gynecology. Hematol Oncol Clin North Am. 2000;14:1061–77–622.
  20. Indexed at, Google Scholar, Crossref

Get the App