Title |
Current trends on immunotherapy for oncology
|
Authors |
Neya Kavya Chander1, A. Prashannalakshmi2, Phanish Chandra Ravi3, Aravind Muthiah4, Yagvalkya Sharma5, Gajalakshmi Suriyanarayanan6,* & P.S Shakthipriya7
|
Affiliation |
1Institute of Internal Medicine, Madras Medical College & Rajiv Gandhi Government General Hospital, Chennai, India; 2Department of Medicine, Tashkent Medical Academy, Urgench branch, Uzbekistan; 3Department of Internal Medicine, SVS Medical College, Mahabubnagar, India; 4Department of Medicine, Tirunelveli Medical College, Tirunelveli, India; 5Department of Research, Kalp Research Work, Mathura, Uttar Pradesh, India; 6Department of Community Medicine, Veer Chandra Singh Garhwali Government Institute of Medical Science and Research, Srinagar, Pauri Garhwal, Uttarakhand, India; 7Institute of Internal Medicine, Madras Medical College, Chennai, India; *Corresponding author
|
|
Neya Kavya Chander - E-mail: nychander01@gmail.com; Phone: +91 9384025898 A Prashannalakshmi - E-mail: prashannahu@gmail.com; Phone: +91 9940594556 Phanish Chandra Ravi - E-mail: phanishchandra183@gmail.com; Phone: +91 9949504761
Aravind Muthiah - E-mail: aravindnobel@gmail.com; Phone: +91
8072027657 Gajalakshmi - E-mail: sgajalakshmi1911@gmail.com; Phone: +91 8197600376 P.S Shakthi Priya - E-mail: shakthipriyaps23@gmail.com; Phone: +91 7305254593
|
Article Type |
Review
|
Date |
Received July 1, 2025; Revised July 31, 2025; Accepted July 31, 2025, Published July 31, 2025
|
Abstract |
Immunotherapy has revolutionized oncology by harnessing the patient’s own immune system to recognize and eliminate tumor cells, leading to durable responses in a variety of malignancies. Over the past decade, immune checkpoint inhibitors targeting CTLA-4, PD-1, and PD-L1 have become standard of care across multiple solid tumors, while chimeric antigen receptor (CAR) T-cell therapies have demonstrated remarkable efficacy in hematologic cancers. Despite these successes, challenges such as primary and acquired resistance, immune-related toxicities, and high treatment costs continue to limit broader application. Emerging strategies including novel checkpoint targets (e.g., LAG-3, TIGIT), next-generation cellular therapies, cancer vaccines, and oncolytic viruses are under active investigation to expand therapeutic options and improve patient outcomes. Biomarker development for patient selection and combination regimens with chemotherapy, targeted agents, and radiation are critical to overcoming resistance mechanisms. Looking ahead, personalized immunotherapy approaches leveraging tumor neoantigens and the tumor microenvironment hold promise for more precise and effective treatments. |
Keywords |
Cancer immunotherapy; immune checkpoint inhibitors; CAR T-cell therapy; tumor microenvironment; immune-related adverse events; precision oncology; combination therapy
|
Citation |
Chander et al. Bioinformation 21(7): 1880-1885 (2025)
|
Edited by |
A Prashanth
|
ISSN |
0973-2063
|
Publisher |
|
License |
This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.
|
|