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The International Journal of the Royal Society of Thailand
              Volume XI - 2019



              prophylactic surgery can also be recommended. When these cancers are detected
              at the earlier state, life expectancy can be extended for these cancer patients.
              The better survival rate based on earlier cancer detection, are likely cost-effective

              health interventions. Since the mutation rates are usually lower than 1%,
              applying the advance screening technology in these number of populations
              are likely a cost-effective strategy. The opening of advance technology service
              platform in the health system also enable the health service system development.
              The screening services development and implementation is the opportunity for
              health service delivery development, especially for the aging populations.

                      Excellent in management shall by applied to deliver the seamless
              integration of genomics medicine from primary care to tertiary care. Family
              health history (FHH) is new tool for screening family at risk for familial cancer,
              the FHH collection process is usually time-consuming steps for routine clinical
              services, but this can be introduced widely due to the primary care cluster
              established in Thailand from 2017. This personalized screening program not
              only vital for cancers prevention in this family. The next generation sequencing
              technology is enabled the liquid biopsy, potentially identify tumors and types
              of tumors even before the clinically detectable stage of cancer. Two of the
              interventions that ready for clinical implementation such as 1) Screening
              program for hereditary breast and ovarian cancer to detect BRCA1/BRCA2
              mutations (King et al., 2003) 2) Screening program for hereditary nonpolyposis
              colorectal cancer or Lynch syndrome to detect mutations in MLH1, MSH2, MSH6,
              PMS2 (Giardiello et al., 2014).

                      In near future, when the sequencing cost reduced further, it is possible
              to provide screening for larger groups at risk, this mean that the screening
              program can included other high-risk populations, and eventually accessible

              to all population.
                      For cancers that caused by oncovirus infection, detection of virus is the
              risk stratification to identify high risk groups for cancer, one prominent example
              is HPV DNA testing in samples from urogenital tract, that identify patients with
              high risk HPV genotype infection. Further investigation can be offered to those
              with high risk HPV genotype infection, so that cervical cancer will be detected

              at the early stage. The HPV DNA test is a better screening test because of its
              better sensitivity, when compared with conventional cytology-based test such as
              “Pap smear”, that looking for abnormal cells from cervix area. Due to the higher



              92                                                   Precision Medicine: Preventive aspect




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