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The Promise and the Hype of 'Personalised Medicine'
1a CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford , Oxford , UK.
Abstract:
Personalised medicine is widely considered as the way of the future for medicine. However, progress in cancer, with a few outstanding exceptions, has fallen below expectations because of the challenges of tumour heterogeneity and clonal evolution. In both benign and malignant disease, diseases caused by single genetic alterations are more amenable to precision medicine approaches. However, most common diseases are caused by a complex interplay of multiple genetic and environmental factors making personalised medicine far more challenging. The current optimism for personalised medicine is distorting clinical consultations, resource allocation and research funding prioritisation. A research active clinician must act both as an agent of change and development, and as a communicator of realism. Thus personalised medicine that includes a sober appreciation of what genomics can achieve, together with continued focus on the individual as a person not just as a genome, will contribute to further improvements in health and healthcare.
Insights
Personalised medicine faces challenges in complex diseases like cancer due to tumour heterogeneity. A realistic approach focusing on genomics and the individual is crucial for future healthcare improvements.
Area of Science:
- Genomic Medicine
- Oncology
- Healthcare Policy
Background:
- Personalised medicine is a highly anticipated future in healthcare.
- Progress in applying personalised medicine to cancer has been limited by tumor heterogeneity and clonal evolution.
- Diseases with single genetic origins are more suitable for precision medicine than complex multifactorial diseases.
Purpose of the Study:
- To critically evaluate the current state and future prospects of personalised medicine.
- To address the challenges hindering the widespread adoption of personalised medicine, particularly in complex diseases.
- To advocate for a balanced perspective on personalised medicine, integrating genomic insights with holistic patient care.
Main Methods:
- Literature review and critical analysis of current research and clinical practices in personalised medicine.
- Examination of the impact of tumour heterogeneity and clonal evolution on cancer treatment.
- Discussion of the complexities of multifactorial diseases in the context of precision medicine.
Main Results:
- The application of personalised medicine in cancer has not met expectations due to significant biological complexities.
- Most common diseases involve intricate genetic and environmental interactions, posing substantial challenges for personalised medicine.
- Current enthusiasm for personalised medicine may be misdirecting clinical resources and research priorities.
Conclusions:
- A realistic appraisal of genomics' capabilities is essential for advancing personalised medicine.
- Focusing on the individual patient beyond their genome is vital for effective healthcare.
- Integrating genomic data with a comprehensive understanding of the patient will drive meaningful health improvements.
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