Your browser doesn't support javascript.
loading
Actionable Mutation Profiles of Non-Small Cell Lung Cancer patients from Vietnamese population.
Dang, Anh-Thu Huynh; Tran, Vu-Uyen; Tran, Thanh-Truong; Thi Pham, Hong-Anh; Le, Dinh-Thong; Nguyen, Lam; Nguyen, Ngoc-Vu; Thi Nguyen, Thai-Hoa; Nguyen, Chu Van; Le, Ha Thu; Thi Nguyen, Mai-Lan; Le, Vu Thuong; Nguyen, Phuc Huu; Vo, Binh Thanh; Thi Dao, Hong-Thuy; Nguyen, Luan Thanh; Van Nguyen, Thien-Chi; Bui, Quynh-Tram Nguyen; Nguyen, Long Hung; Nguyen, Nguyen Huu; Thi Nguyen, Quynh-Tho; Le, Truong Xuan; Do, Thanh-Thuy Thi; Dinh, Kiet Truong; Do, Han Ngoc; Phan, Minh-Duy; Nguyen, Hoai-Nghia; Tran, Le Son; Giang, Hoa.
Afiliação
  • Dang AH; University of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
  • Tran VU; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Tran TT; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Thi Pham HA; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Le DT; Pham Ngoc Thach Hospital, Ho Chi Minh city, Vietnam.
  • Nguyen L; Pham Ngoc Thach Hospital, Ho Chi Minh city, Vietnam.
  • Nguyen NV; Pham Ngoc Thach Hospital, Ho Chi Minh city, Vietnam.
  • Thi Nguyen TH; Vietnam National Cancer Hospital, Ha Noi, Vietnam.
  • Nguyen CV; Vietnam National Cancer Hospital, Ha Noi, Vietnam.
  • Le HT; Ha Noi Oncology hospital, Ha Noi, Vietnam.
  • Thi Nguyen ML; Ha Noi Oncology hospital, Ha Noi, Vietnam.
  • Le VT; Cho Ray hospital, Ho Chi Minh City, Vietnam.
  • Nguyen PH; University of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
  • Vo BT; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Thi Dao HT; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Nguyen LT; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Van Nguyen TC; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Bui QN; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Nguyen LH; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Nguyen NH; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Thi Nguyen QT; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Le TX; University of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
  • Do TT; University of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
  • Dinh KT; Medical Genetics Institute, Ho Chi Minh City, Vietnam.
  • Do HN; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Phan MD; Gene Solutions, Ho Chi Minh city, Vietnam.
  • Nguyen HN; School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Australia.
  • Tran LS; University of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam. nhnghia81@gmail.com.
  • Giang H; Gene Solutions, Ho Chi Minh city, Vietnam. leson1808@gmail.com.
Sci Rep ; 10(1): 2707, 2020 02 17.
Article em En | MEDLINE | ID: mdl-32066856
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenocarcinoma / Regulação Neoplásica da Expressão Gênica / Proteínas Proto-Oncogênicas p21(ras) / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Mutação Tipo de estudo: Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenocarcinoma / Regulação Neoplásica da Expressão Gênica / Proteínas Proto-Oncogênicas p21(ras) / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Mutação Tipo de estudo: Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article