TheScientist's editor Richard Gallagher wrote an interesting editorial in the December issue: Stumbling Toward Personalized Medicine.
Let’s remind ourselves of the three-part promise of personalized medicine. First, everyone’s genome will be sequenced cheaply and the sequence will be interpretable, and predictive. Second, the bulk of a person’s anticipated medical problems, discerned by analysis of the sequence, will be avoided by genetic, lifestyle or therapeutic means. And third, where a disease has to be treated, it will be done with medicines that are exquisitely tailored to both patient and ailment. No risk, no mess, no problem.
The reality (to date) has been dramatically different.
Of course these things never take hold as quickly or thoroughly as we'd like, but there has been progress; numerous companion diagnostics and screens have been developed, and genomic and cellular tests for a wide range of disease states are becoming available (and increasingly they make use of digital pathology, enabling accurate quantification). The editorial does end on a more positive note:
So far we’ve stumbled forward a little on the road to personalized medicine, but it looks like the pace towards Nirvana is about to pick up.
Indeed!
