TY - JOUR
T1 - A clinical trial of somatic and germline analyses for healthy longevity in a postoperative cancer patient
AU - Hayashi, Naoki
AU - Kuroda, Yosuke
AU - Saito, Tomoko
AU - Tsuruda, Yusuke
AU - Niida, Atsushi
AU - Otsu, Hajime
AU - Eguchi, Hidetoshi
AU - Masuda, Takaaki
AU - Suzuki, Yutaka
AU - Natsugoe, Shoji
AU - Mimori, Koshi
N1 - Funding Information:
Fig. 4 The pathways associated with PIK3CA, BRAF, and SMAD4. We assumed that inhibiting proteins coded by these genes or their main downstream molecules was an effective therapeutic strategy Acknowledgements This study was funded by A-STEP (Adaptable and Seamless Technology Transfer Program through Target-driven R & D). The SNP analysis of the salivary sample was performed with the full cooperation of Yahoo Japan Corporation.
Publisher Copyright:
© 2019, Springer Nature Singapore Pte Ltd.
PY - 2019/9/10
Y1 - 2019/9/10
N2 - Purpose: Recent developments in molecular-targeted therapies have improved the clinical outcome of cancer patients; however, the issue of adverse effects due to treatments has often gone unconsidered. We herein report the results of a clinical trial of dual genomic analyses for healthy longevity in a postoperative cancer patient. Methods: We performed dual genomic analyses for a representative 79-year-old rectal cancer patient who relapsed with liver metastasis. First, we determined single-nucleotide polymorphisms according to the constitution and disease risk in the genomic DNA from the patient’s saliva by referring to the data of 10,000 Japanese patients obtained from Yahoo Japan Corporation. Second, we conducted whole-exome sequencing to detect druggable mutations in the primary tumour. Results: Forty of 59 determinable characters related to the constitution were consistent with the clinical phenotype. Several diseases classified as ‘high risk’ diseases actually occurred during the patient’s clinical course. Of the 129 significant mutations, we identified somatic mutations in BRAF, PIK3CA, and SMAD4 as targets. Conclusion: The dual genomic examination will improve the follow-up observation system to support primary care doctors in the social community for taking care of postoperative cancer patients.
AB - Purpose: Recent developments in molecular-targeted therapies have improved the clinical outcome of cancer patients; however, the issue of adverse effects due to treatments has often gone unconsidered. We herein report the results of a clinical trial of dual genomic analyses for healthy longevity in a postoperative cancer patient. Methods: We performed dual genomic analyses for a representative 79-year-old rectal cancer patient who relapsed with liver metastasis. First, we determined single-nucleotide polymorphisms according to the constitution and disease risk in the genomic DNA from the patient’s saliva by referring to the data of 10,000 Japanese patients obtained from Yahoo Japan Corporation. Second, we conducted whole-exome sequencing to detect druggable mutations in the primary tumour. Results: Forty of 59 determinable characters related to the constitution were consistent with the clinical phenotype. Several diseases classified as ‘high risk’ diseases actually occurred during the patient’s clinical course. Of the 129 significant mutations, we identified somatic mutations in BRAF, PIK3CA, and SMAD4 as targets. Conclusion: The dual genomic examination will improve the follow-up observation system to support primary care doctors in the social community for taking care of postoperative cancer patients.
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U2 - 10.1007/s00595-019-01789-7
DO - 10.1007/s00595-019-01789-7
M3 - Article
C2 - 30843125
AN - SCOPUS:85062681659
SN - 0941-1291
VL - 49
SP - 738
EP - 747
JO - Surgery today
JF - Surgery today
IS - 9
ER -