4.6 Article

The genetic landscape of pancreatic head ductal adenocarcinoma in China and prognosis stratification

Journal

BMC CANCER
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12885-022-09279-9

Keywords

Pancreatic cancer; NGS; Genomic landscape; Prognosis prediction

Categories

Funding

  1. National Natural Science Foundation of China [81773109]
  2. Natural Science Foundation of Jiangsu Province [BK20151582]
  3. Nanjing Medical University [2242019K3DN09, 2019DN0011]
  4. Fund of the priority Academic Programme Development of Jiangsu Higher Education Institution [JX1023-1801]
  5. National key Clinical Specialty Construction Project (2014)
  6. Southeast University [2242019K3DN09, 2019DN0011]

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This study analyzed the genomic alterations of 151 Chinese patients with head PDAC and found a higher frequency of KRAS G12V mutation in the Chinese population. Additionally, the authors developed a well-performed nomogram that could improve post-operation care in real-world practice.
Background Pancreatic ductal adenocarcinoma (PDAC) is the major subtype of pancreatic cancer and head PDACs show distinct characteristics from body/tail PDACs. With limited studies based on Asian population, the mutational landscape of Asian PDAC remains unclear. Methods One hundred fifty-one Chinese patients with head PDAC were selected and underwent targeted 425-gene sequencing. Genomic alterations, tumor mutational burden, and microsatellite instability were analyzed and compared with a TCGA cohort. Results The genomic landscape of Chinese and Western head PDAC had identical frequently-mutated genes including KRAS, TP53, SMAD4, and CDKN2A. KRAS hotspot in both cohorts was codon 12 but Chinese PDACs containing more G12V but fewer G12R variants. Potentially pathogenic fusions, CHD2-BRAF and KANK1-MET were identified in two KRAS wild-type patients. Serum cancer antigens CA125 and CA19-9 were positively associated with SMAD4 alterations while high CEA was enriched in wild-type CDKN2A subgroup. The probability of vascular invasion was lower in patients with RNF43 alterations. The nomogram developed including histology grade, the mutation status of SMAD4, TGFBR2, and PREX2 could calculate the risk score of prognoses validated by Chinese and TCGA cohort. Conclusions Chinese head PDAC contained more KRAS G12V mutation than Western population. The well-performed nomogram may improve post-operation care in real-world practice.

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