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Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Targeted Therapy Database (TTD): a model to match patient's molecular profile with current knowledge on cancer
Simone Mocellin1, Jeff Shrager, Richard Scolyer
1Clinica Chirurgica Generale 2, Department of Oncological and Surgical Sciences, University of Padova, Padova, Italy. simone.mocellin@unipd.it
Background:
The efficacy of current anticancer treatments is far from satisfactory and many patients still die of their disease. A general agreement exists on the urgency of developing molecularly targeted therapies, although their implementation in the clinical setting is in its infancy. In fact, despite the wealth of preclinical studies addressing these issues, the difficulty of testing each targeted therapy hypothesis in the clinical arena represents an intrinsic obstacle. As a consequence, we are witnessing a paradoxical situation where most hypotheses about the molecular and cellular biology of cancer remain clinically untested and therefore do not translate into a therapeutic benefit for patients.
Objective:
To present a computational method aimed to comprehensively exploit the scientific knowledge in order to foster the development of personalized cancer treatment by matching the patient's molecular profile with the available evidence on targeted therapy.
Methods:
To this aim we focused on melanoma, an increasingly diagnosed malignancy for which the need for novel therapeutic approaches is paradigmatic since no effective treatment is available in the advanced setting. Relevant data were manually extracted from peer-reviewed full-text original articles describing any type of anti-melanoma targeted therapy tested in any type of experimental or clinical model. To this purpose, Medline, Embase, Cancerlit and the Cochrane databases were searched.
Results And Conclusions:
We created a manually annotated database (Targeted Therapy Database, TTD) where the relevant data are gathered in a formal representation that can be computationally analyzed. Dedicated algorithms were set up for the identification of the prevalent therapeutic hypotheses based on the available evidence and for ranking treatments based on the molecular profile of individual patients. In this essay we describe the principles and computational algorithms of an original method developed to fully exploit the available knowledge on cancer biology with the ultimate goal of fruitfully driving both preclinical and clinical research on anticancer targeted therapy. In the light of its theoretical nature, the prediction performance of this model must be validated before it can be implemented in the clinical setting.
Insights
Developing personalized cancer treatments requires matching patient molecular profiles with targeted therapy evidence. This study presents a computational method to analyze scientific knowledge, aiming to improve targeted therapy development and clinical application for better patient outcomes.
Area of Science:
- Oncology
- Bioinformatics
- Computational Biology
Background:
- Current anticancer treatments have limited efficacy, necessitating molecularly targeted therapies.
- Clinical implementation of targeted therapies is hindered by challenges in testing hypotheses.
- Most cancer biology insights remain clinically untested, limiting therapeutic benefits.
Purpose of the Study:
- To develop a computational method for personalized cancer treatment.
- To match patient molecular profiles with existing targeted therapy evidence.
- To accelerate the translation of cancer research into clinical practice.
Main Methods:
- Focused on melanoma, a malignancy with unmet therapeutic needs.
- Manually extracted data from peer-reviewed articles on anti-melanoma targeted therapies.
- Utilized Medline, Embase, Cancerlit, and Cochrane databases for comprehensive literature search.
Main Results:
- Created a manually annotated database (Targeted Therapy Database, TTD) for computational analysis.
- Developed algorithms to identify prevalent therapeutic hypotheses and rank treatments.
- The method aims to exploit existing knowledge for preclinical and clinical research.
Conclusions:
- The described method provides a framework for analyzing cancer knowledge to guide targeted therapy.
- Algorithms facilitate the identification of optimal treatments based on molecular profiles.
- Further validation is required to implement this model in clinical settings.
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