Tailoring medical treatment to the individual characteristics of each patient.Personalized medicine is an approach to healthcare that tailors medical treatment and prevention strategies to the individual characteristics of each patient, such as their genetic makeup, lifestyle, and environment. This contrasts with the traditional one-size-fits-all model, where treatments are designed for the average patient. By understanding the molecular basis of disease, personalized medicine aims to improve efficacy and reduce adverse effects.
The term gained prominence in the early 2000s following the completion of the Human Genome Project, which provided the foundational data for understanding genetic variation. However, the concept has roots in earlier practices like blood typing for transfusions.
It relies on advanced diagnostics, including genomic sequencing, biomarker analysis, and imaging, to identify the specific drivers of a patient's condition. Clinicians then select therapies that target those drivers, often using drugs or interventions that are most likely to work for that particular genetic profile. This can involve pharmacogenomics, which studies how genes affect a person's response to drugs.
Personalized medicine is used in oncology to choose targeted cancer therapies based on tumor mutations, in cardiology to adjust drug dosages based on genetic variants, and in rare disease diagnosis through whole-exome sequencing.
The first FDA-approved drug with a pharmacogenomic label was the leukemia drug mercaptopurine, which requires dose adjustment based on a patient's TPMT gene variant.















