Pan‐cancer molecular analysis of EGFR large fragment deletion in the Asian population

Author:

Pu Jun1,Guo Huannan2,Yu Ruoying3ORCID,Ou Qiuxiang3ORCID,Bao Hua3,Wu Xue3,Tang Sanyuan45,Chang Qingyong6

Affiliation:

1. Department of Neurosurgery Second Hospital of Kunming Medical University Kunming China

2. Department of Medical Oncology General Hospital of Heilongjiang Province Land Reclamation Bureau Harbin People's Republic of China

3. Nanjing Geneseeq Technology Inc. Nanjing China

4. Department of Oncology The Affiliated Nanhua Hospital, Hengyang Medical School, University of South China Hengyang China

5. Oncology Department The Second People's Hospital of Hunan Province Changsha China

6. The Department of Neurosurgery Affiliated Zhongshan Hospital of Dalian University Dalian China

Abstract

AbstractBackgroundLarge fragment deletion (LFD) of EGFR was associated with carcinogenesis in many types of cancers. However, the molecular features of EGFR‐LFD have not been studied in the Asian cancer population.MethodHere we retrospectively analyzed the targeted sequencing data from a large cancer database.ResultsEGFR‐LFD was detected at a frequency of 0.03% with EGFRvIII being the most frequently observed LFD. TERTp variants were identified in 60% of the cases. TP53 alterations (33%) were mutually exclusive with TERTp variants and coexisted with EGFR‐LFD in lung cancer and colorectal cancer. EGFR amplification (67%) and chromosome 10p deletion (53%) were the most focal‐level and arm‐level CNV in this cohort. EGFR exon2–17 skipping was found in the tumor tissue of one patient after progressing on osimertinib.ConclusionOur study provided valuable insights into the distribution and molecular characteristics of EGFR‐LFD, hoping to shed light on the treatment management for EGFR‐LFD carriers.

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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