Creation of the Swiss group of Pharmacogenomics and personalised Therapy (SPT)
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Ursula Amstutz
und on behalf of the Swiss group of Pharmacogenomics and Personalised Therapy
In memory of Prof. Gérard Siest († April 9th, 2016) and in honour of his contribution to the creation of SPT
With the development of modern drugs, it quickly became apparent that not all individuals respond equally to drug therapy. Outcomes can be multiple, ranging from a good response to non-efficacy or to the development of adverse drug reactions. Differences in response are partly attributed to various environmental factors and to an individual’s genetic predisposition as well [1]. The progress of molecular sciences has enabled both an improved understanding of drug mechanism, and of underlying molecular differences between individuals that influence the pharmacokinetics and pharmacodynamics of drugs. In turn, this provides an opportunity to identify individuals who will react differently to a given drug based on their genetic characteristics. The study of how individuals respond to drugs due to their genetic background has been termed “pharmacogenetics” or “pharmacogenomics” [1]. Bringing together clinicians and scientists in various fields, such as pharmacology, genetics, molecular biology and laboratory medicine, pharmacogenomics is a multidisciplinary science with great potential to translate findings to benefit patients by individualising therapy and providing new targets for drug development [1].
Combining multiple scientific disciplines and research approaches entails the need for a platform that is broad enough to be able to address challenges and further advance individualised medicine. For this reason, the European Society of Pharmacogenomics and Personalised Therapy (ESPT; President: Professor Ron HN van Schaik, Erasmus University Medical Center Rotterdam, The Netherlands) was established to offer the opportunity to exchange information and share ideas over a broad spectrum of scientific disciplines [2]. The aim of the ESPT is to promote “leadership and innovation in science and education to enhance the scientific basis and quality of diagnosis and therapy for patients throughout the world.” The ESPT welcomes experts from various fields of basic molecular and biochemical sciences, to clinically oriented sciences, along with practitioners, such as hospital clinicians, pharmacologists and pharmacists. The society emphasizes an informal structure that allows for personal initiative. For this reason, the creation of national pharmacogenomics societies was a key vision of the late president of ESPT, Prof. Gérard Siest. Today, the ESPT is present throughout most of Europe through national societies that serve to organize and promote pharmacogenomics research. To add to this growing number of national efforts, on February 3rd 2016, a constitution meeting of the Swiss Group of Pharmacogenomics and personalised Therapy (SPT) was held in Bern, Switzerland. The SPT was created by researchers who are active in the field of pharmacogenomics as a section within the Swiss Society of Clinical Pharmacology and Toxicology (SSCPT, then President: Dr. Hugo Kupferschmidt, Tox Info Suisse, Zurich, Switzerland; current President: Professor Thierry Buclin, Lausanne University Hospital CHUV, Switzerland) and will serve as a Swiss national point for the ESPT. As a country investing one of the highest percentages of its BDP in science and development, Switzerland has a strong commitment to fostering innovation in medical and pharmaceutical sciences. In addition, there exists a longstanding university-industry partnership culture that is underpinned by a strong base in the pharmaceutical and biotechnology industry. Indeed, as a society encouraging dynamic national and international activity, ESPT has warmly welcomed the creation of the SPT.
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved its submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
References
1. Wang L. Pharmacogenomics: a systems approach. Wiley Interdiscip Rev Syst Biol Med 2010;2:3–22.10.1002/wsbm.42Suche in Google Scholar PubMed PubMed Central
2. An update from The European Society of Pharmacogenomics and Theranostics. Pharmacogenomics 2012;13:133–5.10.2217/pgs.11.188Suche in Google Scholar
©2017 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- Editorial
- Creation of the Swiss group of Pharmacogenomics and personalised Therapy (SPT)
- Publisher’s Note
- Swarup A.V. Shah won the poster award at the 4th Annual Conference of ESPT
- Original Articles
- COQ2 polymorphisms are not associated with increased risk of statin-induced myalgia/myopathy in the Czech population
- Role of CYP4F2, CYP2C19, and CYP1A2 polymorphisms on acenocoumarol pharmacogenomic algorithm accuracy improvement in the Greek population: need for sub-phenotype analysis
- Estimation of fractions metabolized by hepatic CYP enzymes using a concept of inter-system extrapolation factors (ISEFs) – a comparison with the chemical inhibition method
- In vitro modulation of the cytochrome P450 and ABCB1/P-glycoprotein activities of the aqueous extract of Allophylus cominia (L) Sw. leaves
- Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
- Drug-drug interactions in cancer chemotherapy: an observational study in a tertiary health care centre
- Acknowledgment
Artikel in diesem Heft
- Frontmatter
- Editorial
- Creation of the Swiss group of Pharmacogenomics and personalised Therapy (SPT)
- Publisher’s Note
- Swarup A.V. Shah won the poster award at the 4th Annual Conference of ESPT
- Original Articles
- COQ2 polymorphisms are not associated with increased risk of statin-induced myalgia/myopathy in the Czech population
- Role of CYP4F2, CYP2C19, and CYP1A2 polymorphisms on acenocoumarol pharmacogenomic algorithm accuracy improvement in the Greek population: need for sub-phenotype analysis
- Estimation of fractions metabolized by hepatic CYP enzymes using a concept of inter-system extrapolation factors (ISEFs) – a comparison with the chemical inhibition method
- In vitro modulation of the cytochrome P450 and ABCB1/P-glycoprotein activities of the aqueous extract of Allophylus cominia (L) Sw. leaves
- Thymidylate synthase gene variants as predictors of clinical response and toxicity to fluoropyrimidine-based chemotherapy for colorectal cancer
- Drug-drug interactions in cancer chemotherapy: an observational study in a tertiary health care centre
- Acknowledgment