Evidence map›Paper›PMID 32066856›Full record

ArticleScientific reports2020

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

Anh-Thu Huynh Dang, Vu-Uyen Tran, Thanh-Truong Tran, Hong-Anh Thi Pham, Dinh-Thong Le, Lam Nguyen, Ngoc-Vu Nguyen, Thai-Hoa Thi Nguyen, Chu Van Nguyen, Ha Thu Le and 19 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05227261 (Assessment of a Novel Blood Test in Early Detection of the Five Common Cancers Based on the Investigation of the Circulating Tumour DNA), which is not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05227261 completednot on this mapstarted 2022, after this paper: background citation

Assessment of a Novel Blood Test in Early Detection of the Five Common Cancers Based on the Investigation of the Circulating Tumour DNA

TypeobservationalSponsorGene SolutionsRan2022 to 2024Enrolled9,057ConditionsCancer, Lung, Cancer, Breast, Cancer Liver, Cancer, Colorectal
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. A KRASMolecular therapy. Oncology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Prevalence ofLung Cancer (Auckland, N.Z.) · 2025
    Article
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  10. Article
  11. Article
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  15. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors at 8 institutions in 3 countries.

Anh-Thu Huynh Dang *University of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
Vu-Uyen Tran *Gene Solutions, Ho Chi Minh city, Vietnam.
Thanh-Truong TranGene Solutions, Ho Chi Minh city, Vietnam.
Hong-Anh Thi PhamGene Solutions, Ho Chi Minh city, Vietnam.
Dinh-Thong LePham Ngoc Thach Hospital, Ho Chi Minh city, Vietnam.
Lam NguyenPham Ngoc Thach Hospital, Ho Chi Minh city, Vietnam.
Ngoc-Vu NguyenPham Ngoc Thach Hospital, Ho Chi Minh city, Vietnam.
Thai-Hoa Thi NguyenVietnam National Cancer Hospital, Ha Noi, Vietnam.
Chu Van NguyenVietnam National Cancer Hospital, Ha Noi, Vietnam.
Ha Thu LeHa Noi Oncology hospital, Ha Noi, Vietnam.
Mai-Lan Thi NguyenHa Noi Oncology hospital, Ha Noi, Vietnam.
Vu Thuong LeCho Ray hospital, Ho Chi Minh City, Vietnam.
Phuc Huu NguyenUniversity of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
Binh Thanh VoGene Solutions, Ho Chi Minh city, Vietnam.
Hong-Thuy Thi DaoGene Solutions, Ho Chi Minh city, Vietnam.
Luan Thanh NguyenGene Solutions, Ho Chi Minh city, Vietnam.
Thien-Chi Van NguyenGene Solutions, Ho Chi Minh city, Vietnam.
Quynh-Tram Nguyen BuiGene Solutions, Ho Chi Minh city, Vietnam.
Long Hung NguyenGene Solutions, Ho Chi Minh city, Vietnam.
Nguyen Huu NguyenGene Solutions, Ho Chi Minh city, Vietnam.
Quynh-Tho Thi NguyenMedical Genetics Institute, Ho Chi Minh City, Vietnam.
Truong Xuan LeUniversity of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
Thanh-Thuy Thi DoUniversity of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam.
Kiet Truong DinhMedical Genetics Institute, Ho Chi Minh City, Vietnam.
Han Ngoc DoGene Solutions, Ho Chi Minh city, Vietnam.
Minh-Duy PhanGene Solutions, Ho Chi Minh city, Vietnam.
Hoai-Nghia NguyenUniversity of Medicine and Pharmacy at Ho Chi Minh city, Ho Chi Minh city, Vietnam. nhnghia81@gmail.com.
Le Son TranGene Solutions, Ho Chi Minh city, Vietnam. leson1808@gmail.com.ORCID http://orcid.org/0000-0002-5382-3903
Hoa GiangGene Solutions, Ho Chi Minh city, Vietnam. gianghoa@gmail.com.
Pham Ngoc Thach Hospital · VNUniversity of Medicine and Pharmacy at Ho Chi Minh City · VNAgricultural Genetics Institute · VNVietnam National Children's Hospital · VNCho Ray Hospital · VNThe University of Queensland · AUUniversity Medical Center HCMC · VNUniversity of Economics Ho Chi Minh City · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Gene Expression Regulation, NeoplasticMutationAdenocarcinomaAdultAgedAged, 80 and overAnaplastic Lymphoma KinaseAsian PeopleCarcinoma, Non-Small-Cell LungDNA Mutational AnalysisErbB ReceptorsFemaleGTP PhosphohydrolasesHigh-Throughput Nucleotide SequencingHumansIncidenceALK protein, humanAnaplastic Lymphoma KinaseBRAF protein, humanEGFR protein, humanErbB ReceptorsGTP PhosphohydrolasesKRAS protein, humanMembrane ProteinsNRAS protein, humanProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)ROS1 protein, human

Identifiers

PMID32066856
PMCPMC7026432
OpenAlexW3006608335

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.