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Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Molecular targeted therapy in prevalent tumors: learning from the past and future perspectives
Otto Metzger-Filho1, Camilo Moulin, Ahmad Awada
1Medical Oncology Clinic, Jules Bordet Institute, Brussels, Belgium.
Abstract:
Important advances have been achieved with molecular targeted agents in clinical oncology. Breast, colon, and lung cancer, are now commonly treated with a combination of chemotherapy and targeted agents. In this article the authors discuss the limitations of targeted therapy development, failures of previous studies, and possible strategies for an intelligent drug development. Initial attempts to block mTOR in breast cancer, the magnitude of benefit obtained with anti-EGFR therapy in lung cancer, and the narrowing use of anti-EGFR therapy in colon cancer based on KRAS status are discussed.
Insights
Molecular targeted agents have advanced cancer treatment, but development faces limitations. Strategies for intelligent drug development are crucial for overcoming failures in treating breast, colon, and lung cancers.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Molecular targeted agents represent significant advances in clinical oncology.
- These agents are commonly combined with chemotherapy for breast, colon, and lung cancers.
- Despite progress, targeted therapy development encounters limitations and past study failures.
Purpose of the Study:
- To discuss the limitations encountered in molecular targeted agent development.
- To analyze failures from previous targeted therapy studies.
- To propose strategies for more intelligent drug development in oncology.
Main Methods:
- Review of existing literature on molecular targeted agents in oncology.
- Analysis of specific case studies including mTOR inhibitors in breast cancer.
- Examination of anti-EGFR therapy efficacy in lung and colon cancer, considering KRAS mutation status.
Main Results:
- Initial mTOR blockade attempts in breast cancer showed limited benefit.
- Anti-EGFR therapy demonstrated significant benefit in lung cancer.
- Colon cancer treatment with anti-EGFR therapy is increasingly guided by KRAS mutation status.
Conclusions:
- Targeted therapy development requires overcoming significant limitations and past failures.
- Intelligent drug development strategies are necessary for optimizing cancer treatment.
- Personalized approaches, like KRAS-based selection for anti-EGFR therapy, are vital.
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