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In Vivo Immunofluorescence Localization for Assessment of Therapeutic and Diagnostic Antibody Biodistribution in Cancer Research
Published on: September 16, 2019
Antibodies and their multivalent constructs for cancer therapy
1Department of Chemistry and Biochemistry, The University of Texas at Austin, MBB 3.310, 2500 speedway, Austin, Texas 78712. qingli2012@utexas.edu.
Abstract:
In 2008 cancer was identified by the World Health Organization (WHO) as one of four threats to human health and development. Since the early published reports of the first chemotherapeutic, mustine, in 1946, the anti-cancer drug and development industry has grown into a multi-billion dollar business enterprise. Worldwide, the rates of new cancer cases and deaths has been steadily increasing each year, with the estimation by the WHO-sponsored GLOBOCAN cancer database, that at current rates, nearly 13 million cancer deaths will be reported in 2030. The recent successes of monoclonal antibodies (mAbs), an important class of glycoprotein, and their multivalent and drug conjugated derivatives over the past 30 years have led to the approval of 12 monoclonal antibodies for use in cancer treatment by the FDA. Modern recombinant and engineering techniques have led to an explosion of antibody platforms that can be attributed to great gains in clinical efficacy. This review discusses and outlines a sample of mAbs currently approved for cancer treatment by the FDA, as well as antibody platforms in the research pipeline and clinic that have been engineered for greater tumor penetration, binding, and efficacy.
Insights
Monoclonal antibodies (mAbs) are increasingly successful in treating cancer, with FDA-approved options and promising new antibody platforms in development for enhanced efficacy and tumor targeting.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Cancer remains a significant global health threat, with increasing incidence and mortality rates.
- The anti-cancer drug industry has expanded significantly since the mid-20th century.
- Monoclonal antibodies (mAbs) represent a key advancement in cancer therapeutics.
Purpose of the Study:
- To review currently FDA-approved monoclonal antibodies for cancer treatment.
- To discuss emerging antibody platforms in clinical research and development.
- To highlight advancements in antibody engineering for improved anti-cancer efficacy.
Main Methods:
- Review of FDA-approved monoclonal antibodies for cancer therapy.
- Analysis of antibody platforms in the research and clinical pipeline.
- Discussion of engineering techniques enhancing antibody tumor penetration, binding, and efficacy.
Main Results:
- Twelve monoclonal antibodies have been approved by the FDA for cancer treatment.
- Recombinant and engineering techniques have driven significant gains in antibody-based cancer therapy efficacy.
- New antibody platforms are being developed for superior tumor targeting and therapeutic effect.
Conclusions:
- Monoclonal antibodies are a vital and growing component of modern cancer treatment.
- Ongoing research and engineering innovations promise further improvements in antibody-based cancer therapies.
- Advanced antibody platforms offer potential for enhanced tumor penetration, binding, and overall clinical efficacy.
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