There’s a good reason why precision medicine sparks such excitement and controversy. It promises individualized diagnosis and targeted therapy that can treat the most challenging and incurable of diseases — yet the numerous obstacles standing in its way, such as regulatory approvals and affordability, call into question its wide-scale application. Still, precision medicine continues to gain momentum in APAC, affirming our belief that it will play a crucial role in delivering effective healthcare to the region in the near future.
In its first series of publications, L.E.K. Consulting’s APAC Life Sciences Centre of Excellence will explore the key aspects of precision medicine for APAC: its potential contribution to the region, leading innovators in the space, hurdles to overcome and the role various stakeholders will play in influencing the rate of adoption of precision medicine in this region. This initial publication offers an overview of some of the elements critical for precision medicine to succeed in APAC, which will be studied in further detail in subsequent publications.
Building the foundation
Over the past two decades, the West has helped pave the way for precision medicine. In 2003, the Human Genome Project published the full genome sequence, following a detailed analysis of the structure, organization and function of human genes. The landmark international research initiative has since spurred the creation of large DNA repositories, including public efforts such as the Human Genome Diversity Project and the 1000 Genomes Project, as well as databanks created by genealogy companies such as 23andMe, Ancestry and more. Meanwhile, disease-focused database development is also underway, with public data portals led by organizations such as The Cancer Genome Atlas and the International Cancer Genome Consortium, along with similar private efforts sponsored by companies including Foundation Medicine and Caris Life Sciences. These databases have continued to grow in size and sophistication over the years and serve as a treasure trove of information aiding the development of gene-specific therapies.
Existing databases, unfortunately, are overwhelmingly made up of Caucasians’ data. For APAC to fully reap the benefits of precision medicine, it will first have to collect sufficient data on APAC genotypes. Only then can diagnosis and treatment be appropriately tailored to diseases disproportionately affecting this region. Equally important will be the quality of data gathered; there has to be adequate diversity to accurately capture the genetic traits of specific subsets of the APAC population.
Nonetheless, as the cost of genome sequencing continues to decline exponentially, we expect APAC to catch up over the coming few years thanks to a combination of consumer genetic testing companies and government-led programs. In fact, efforts are already underway. The GenomeAsia100K initiative, for example, is a multicountry collaboration that seeks to “sequence and analyse 100,000 Asian individuals’ genomes to help accelerate Asian population-specific medical advances and precision medicine.” All findings and results will be shared with the broader scientific community so that the responsibility of furthering the industry through R&D is spread among other similar institutions and organizations.





