Monoclonal Antibodies and Clinical Use in the Field of Cancer Treatment

Authors

  • Sabrina Hui-Yan Chao

DOI:

https://doi.org/10.61173/26ve7g24

Keywords:

Monoclonal therapeutics, personalised treatments, monoclonal antibody production, cancer treatment, cancer immunotherapy

Abstract

Monoclonal antibody-based cancer therapy has now been proven successful and effective in the therapeutic treatment of both haematological malignancies and solid tumours. Antibodies are proteins that bind to specific antigens naturally circulating in the body, and monoclonal antibodies are designed to mimic this biological process. Possessing high specificity, monoclonal antibodies can be engineered to directly target cancerous cells, making them highly valuable in clinical settings as they cause minimal damage to non-cancerous cells. As an emerging technology in cancer treatment, they are used alongside established methods such as surgery, radiotherapy, and chemotherapy. This paper explores the historical development of monoclonal antibodies, detailing their production processes and examining current clinical applications in cancer treatment, along with the controversies surrounding their use. It also assesses the balance between the economic costs associated with monoclonal antibody therapies and their clinical success, while drawing comparisons with other newly emerging therapeutic technologies in the field. By synthesizing these elements, the paper aims to provide a comprehensive overview of the role of monoclonal antibodies in cancer treatment and their position within the broader landscape of oncology therapies.

References

[1] Traditional Hybridoma Techniques - innovations, benefits & future. Retrieved from Danaher life sciences. (2024, May 10).

[2] Ecker, Dawn M et al. “The therapeutic monoclonal antibody market.” mAbs vol. 7,1 (2015): 9-14.

[3] Leavy, O. The birth of monoclonal antibodies. Nat Immunol 17 (Suppl 1), S13 (2016).

[4] Chapman, Andrew P. “PEGylated antibodies and antibody fragments for improved therapy: a review.” Advanced drug delivery reviews vol. 54,4 (2002): 531-45.

[5] Cleveland Clinic. ELISA. Retrieved from Cleveland Clinic. (2023, May 15).

[6] McKinnon, Katherine M. “Flow Cytometry: An Overview.” Current protocols in immunology vol. 120 5.1.1-5.1.11. 21 Feb. 2018.

[7] Ravandi, Farhad, and Susan O’Brien. “Alemtuzumab.” Expert review of anticancer therapy vol. 5,1 (2005): 39-51.

[8] Alinari, L et al. “Alemtuzumab (Campath-1H) in the treatment of chronic lymphocytic leukemia.” Oncogene vol. 26,25 (2007): 3644-53.

[9] Pento, Joseph Thomas. “Monoclonal Antibodies for the Treatment of Cancer.” Anticancer research vol. 37,11 (2017): 5935-5939.

[10] Healio. FDA aoorives second-line bevacizumab plus chemo for metastatic colorectal cancer. Retrieved from Healio. (2006, July 1).

[11] Nahta, R, and F J Esteva. “Trastuzumab: triumphs and tribulations.” Oncogene vol. 26,25 (2007): 3637-43.

[12] Shpilberg, O, and C Jackisch. “Subcutaneous administration of rituximab (MabThera) and trastuzumab (Herceptin) using hyaluronidase.” British journal of cancer vol. 109,6 (2013): 1556-61.

[13] Pohlmann, Paula R et al. “Resistance to Trastuzumab in Breast Cancer.” Clinical cancer research: an official journal of the American Association for Cancer Research vol. 15,24 (2009): 7479-7491

[14] Chames, Patrick et al. “Therapeutic antibodies: successes, limitations and hopes for the future.” British journal of pharmacology vol. 157,2 (2009): 220-33.

[15] Liu, Jiwei et al. “Unveiling the new chapter in nanobody engineering: advances in traditional construction and AI-driven optimization.” Journal of nanobiotechnology vol. 23,1 87. 6 Feb. 2025.

Downloads

Published

2025-12-19