Actionable Mutation Profiles of Non-Small Cell Lung Cancer patients from Vietnamese population

被引:22
|
作者
Anh-Thu Huynh Dang [1 ]
Vu-Uyen Tran [2 ]
Thanh-Truong Tran [2 ]
Hong-Anh Thi Pham [2 ]
Dinh-Thong Le [3 ]
Lam Nguyen [3 ]
Ngoc-Vu Nguyen [3 ]
Thai-Hoa Thi Nguyen [4 ]
Chu Van Nguyen [4 ]
Ha Thu Le [5 ]
Mai-Lan Thi Nguyen [5 ]
Vu Thuong Le [6 ]
Phuc Huu Nguyen [1 ]
Binh Thanh Vo [2 ]
Hong-Thuy Thi Dao [2 ]
Luan Thanh Nguyen [2 ]
Thien-Chi Van Nguyen [2 ]
Quynh-Tram Nguyen Bui [2 ]
Long Hung Nguyen [2 ]
Nguyen Huu Nguyen [2 ]
Quynh-Tho Thi Nguyen [7 ]
Truong Xuan Le [1 ]
Thanh-Thuy Thi [1 ]
Kiet Truong Dinh [7 ]
Han Ngoc Do [2 ]
Minh-Duy Phan [2 ,8 ]
Hoai-Nghia Nguyen [1 ]
Le Son Tran [2 ,9 ]
Giang, Hoa [2 ,7 ]
机构
[1] Univ Med & Pharm Ho Chi Minh City, Ho Chi Minh City, Vietnam
[2] Gene Solut, Ho Chi Minh City, Vietnam
[3] Pham Ngoc Thach Hosp, Ho Chi Minh City, Vietnam
[4] Vietnam Natl Canc Hosp, Hanoi, Vietnam
[5] Ha Noi Oncol Hosp, Hanoi, Vietnam
[6] Cho Ray Hosp, Ho Chi Minh City, Vietnam
[7] Med Genet Inst, Ho Chi Minh City, Vietnam
[8] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld, Australia
[9] Astar, Inst Mol & Cellular Biol, Singapore, Singapore
关键词
MOLECULAR TESTING GUIDELINE; ONCOGENIC DRIVER MUTATIONS; KRAS MUTATIONS; EGFR MUTATIONS; CLINICAL-FEATURES; RESISTANCE; ADENOCARCINOMAS; ALK; REARRANGEMENTS; EPIDEMIOLOGY;
D O I
10.1038/s41598-020-59744-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Comprehensive profiling of actionable mutations in non-small cell lung cancer (NSCLC) is vital to guide targeted therapy, thereby improving the survival rate of patients. Despite the high incidence and mortality rate of NSCLC in Vietnam, the actionable mutation profiles of Vietnamese patients have not been thoroughly examined. Here, we employed massively parallel sequencing to identify alterations in major driver genes (EGFR, KRAS, NRAS, BRAF, ALK and ROS1) in 350 Vietnamese NSCLC patients. We showed that the Vietnamese NSCLC patients exhibited mutations most frequently in EGFR (35.4%) and KRAS (22.6%), followed by ALK (6.6%), ROS1 (3.1%), BRAF (2.3%) and NRAS (0.6%). Interestingly, the cohort of Vietnamese patients with advanced adenocarcinoma had higher prevalence of EGFR mutations than the Caucasian MSK-IMPACT cohort. Compared to the East Asian cohort, it had lower EGFR but higher KRAS mutation prevalence. We found that KRAS mutations were more commonly detected in male patients while EGFR mutations was more frequently found in female. Moreover, younger patients (<61 years) had higher genetic rearrangements in ALK or ROS1. In conclusions, our study revealed mutation profiles of 6 driver genes in the largest cohort of NSCLC patients in Vietnam to date, highlighting significant differences in mutation prevalence to other cohorts.
引用
收藏
页数:11
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