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Updated: May 28, 2025

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Innovation in cancer pharmacotherapy through integrative consideration of germline and tumor genomes
Roman Tremmel1, Daniel Hübschmann2, Elke Schaeffeler3
1Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, Germany; University of Tuebingen, Tuebingen, Germany.
Abstract:
Precision cancer medicine is widely established, and numerous molecularly targeted drugs for various tumor entities are approved or are in development. Personalized pharmacotherapy in oncology has so far been based primarily on tumor characteristics, for example, somatic mutations. However, the response to drug treatment also depends on pharmacological processes summarized under the term ADME (absorption, distribution, metabolism, and excretion). Variations in ADME genes have been the subject of intensive research for >5 decades, considering individual patients' genetic makeup, referred to as pharmacogenomics (PGx). The combined impact of a patient's tumor and germline genome is only partially understood and often not adequately considered in cancer therapy. This may be attributed, in part, to the lack of methods for combined analysis of both data layers. Optimized personalized cancer therapies should, therefore, aim to integrate molecular information, which derives from both the tumor and the germline genome, and taking into account existing PGx guidelines for drug therapy. Moreover, such strategies should provide the opportunity to consider genetic variants of previously unknown functional significance. Bioinformatic analysis methods and corresponding algorithms for data interpretation need to be developed to integrate PGx data in cancer therapy with a special meaning for interdisciplinary molecular tumor boards, in which cancer patients are discussed to provide evidence-based recommendations for clinical management based on individual tumor profiles. SIGNIFICANCE STATEMENT: The era of personalized oncology has seen the emergence of drugs tailored to genetic variants associated with cancer biology. However, the full potential of targeted therapy remains untapped owing to the predominant focus on acquired tumor-specific alterations. Optimized cancer care must integrate tumor and patient genomes, guided by pharmacogenomic principles. An essential prerequisite for realizing truly personalized drug treatment of cancer patients is the development of bioinformatic tools for comprehensive analysis of all data layers generated in modern precision oncology programs.
Insights
Precision cancer medicine needs to integrate both tumor and patient genetic data. Incorporating pharmacogenomics (PGx) and advanced bioinformatics can optimize personalized cancer therapies for better patient outcomes.
Area of Science:
- Oncology
- Genomics
- Pharmacology
Background:
- Precision cancer medicine currently focuses mainly on tumor-specific mutations.
- Patient response to cancer drugs is also influenced by absorption, distribution, metabolism, and excretion (ADME) processes.
- Pharmacogenomic (PGx) variations in ADME genes are crucial for personalized drug response.
Purpose of the Study:
- To highlight the necessity of integrating tumor and germline genomic data in cancer therapy.
- To emphasize the role of pharmacogenomics (PGx) in optimizing personalized cancer treatments.
- To advocate for the development of bioinformatics tools for combined genomic data analysis.
Main Methods:
- Review of current practices in precision cancer medicine.
- Discussion of the impact of ADME gene variations on drug efficacy.
- Emphasis on the need for integrated analysis of tumor and germline genomes.
Main Results:
- Current personalized oncology predominantly relies on tumor genetic profiles.
- The combined influence of tumor and germline genomes on drug response is not fully understood or utilized.
- Existing PGx guidelines offer a foundation for integrating germline information.
Conclusions:
- Optimized personalized cancer therapies require the integration of tumor and germline genomic data.
- Bioinformatic tools are essential for analyzing and interpreting combined genomic data.
- Interdisciplinary molecular tumor boards can leverage integrated data for evidence-based recommendations.
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