Evidence map›Paper›PMID 29747488›Full record

ArticleCancer research and treatment2019

Investigating the Feasibility of Targeted Next-Generation Sequencing to Guide the Treatment of Head and Neck Squamous Cell Carcinoma.

Sun Min Lim, Sang Hee Cho, In Gyu Hwang, Jae Woo Choi, Hyun Chang, Myung-Ju Ahn, Keon Uk Park, Ji-Won Kim, Yoon Ho Ko, Hee Kyung Ahn and 19 more

Open access · diamondAbstract readMulticenter Study
In one paragraph

Article in Cancer research and treatment, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.7field-weighted citation impact, top 17% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Immune biomarkers for head and neck cancer.Cancer immunology, immunotherapy : CII · 2025
    Review
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  10. Extracellular vesicles as tools and targets in therapy for diseases.Signal transduction and targeted therapy · 2024
    Review
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  15. Review
  16. Review
  17. Frontiers in immunology · 2022
    Article
  18. Article
  19. Review
  20. Review
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 20 institutions in 1 country.

Sun Min LimDivision of Medical Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, Korea.
Sang Hee ChoDepartment of Hemato-Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
In Gyu HwangDivision of Hematology/Oncology, Department of Internal Medicine, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea.
Jae Woo ChoiDepartment of Pharmacology, Severance Biomedical Science Institute, Yonsei University of College of Medicine, Yonsei Cancer Research Institute, JE-UK Laboratory of Molecular Cancer Therapeutics, Seoul, Korea.
Hyun ChangDivision of Hematology and Medical Oncology, International St. Mary's Hospital, Catholic Kwandong University College of Medicine, Incheon, Korea.
Myung-Ju AhnDepartment of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Keon Uk ParkDepartment of Hemato-Oncology, Keimyung University Dongsan Medical Center, Daegu, Korea.
Ji-Won KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Yoon Ho KoDepartment of Internal Medicine, Uijeongbu St. Mary's Hospital, Uijeongbu, Korea.
Hee Kyung AhnDepartment of Medical Oncology, Gachon University Gil Medical Center, Incheon, Korea.
Byoung Chul ChoDivison of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.
Byung-Ho NamHERINGS, The Institute of Advanced Clinical & Biomedical Research, Seoul, Korea.
Sang Hoon ChunDivision of Medical Oncology, Department of Internal Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Korea.
Ji Hyung HongDepartment of Internal Medicine, Incheon St. Mary's Hospital, Incheon, Korea.
Jung Hye KwonDivision of Hemato-Oncology, Department of Internal Medicine, Hallym University Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.
Jong Gwon ChoiDepartment of Internal Medicine, Konyang University Hospital, Daejeon, Korea.
Eun Joo KangDivision of Medical Oncology, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea.
Tak YunRare Cancers Clinic, Center for Specific Organs Cancer, National Cancer Center, Goyang, Korea.
Keun-Wook LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Joo-Hang KimDivision of Medical Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, Korea.
Jin Soo KimDepartment of Internal Medicine, SMG-SNU Boramae Hospital, Seoul, Korea.
Hyun Woo LeeDepartment of Hematology-Oncology, Ajou University School of Medicine, Suwon, Korea.
Min Kyoung KimDepartment of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea.
Dongmin JungDepartment of Pharmacology, Institute for Cancer Research, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.
Ji Eun KimDepartment of Pathology, SMG-SNU Boramae Hospital, Seoul National University College of Medicine, Seoul, Korea.
Bhumsuk KeamDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Hwan Jung YunDepartment of Internal Medicine, Chungnam National University Hospital, Daejeon, Korea.
Sangwoo KimDepartment of Biomedical Systems Informatics and Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
Hye Ryun KimDivison of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.
Yonsei University · KRSNUH SMG-SNU Boramae Medical Center · KRCHA University Bundang Medical Center · KRAjou University · KRCatholic Kwandong University · KRCatholic University of Korea · KRChonnam National University Hwasun Hospital · KRChung-Ang University Hospital · KRChungnam National University Hospital · KRGachon University Gil Medical Center · KRKangdong Sacred Heart Hospital · KRKeimyung University · KRKonyang University Hospital · KRKorea University Medical Center · KRNational Cancer Center · KRSeoul National University Bundang Hospital · KRSeoul National University Hospital · KRSungkyunkwan University · KRThe Catholic University of Korea Incheon St. Mary's Hospital · KRThe Catholic University of Korea Uijeongbu St. Mary's Hospital · KR

Funding

Ministry of Health and Welfare 1631050
6 · The paper itself

Abstract

purposeHead and neck squamous cell carcinoma (HNSCC) is a deadly disease in which precision medicine needs to be incorporated. We aimed to implement next-generation sequencing (NGS) in determining actionable targets to guide appropriate molecular targeted therapy in HNSCC patients. MATERIALS AND

methodsNinety-three tumors and matched blood samples underwent targeted sequencing of 244 genes using the Illumina HiSeq 2500 platform with an average depth of coverage of greater than 1,000×. Clinicopathological data from patients were obtained from 17 centers in Korea, and were analyzed in correlation with NGS data.

resultsNinety-two of the 93 tumors were amenable to data analysis. TP53 was the most common mutation, occurring in 47 (51%) patients, followed by CDKN2A (n=23, 25%), CCND1 (n=22, 24%), and PIK3CA (n=19, 21%). The total mutational burden was similar between human papillomavirus (HPV)-negative vs. positive tumors, although TP53, CDKN2A and CCND1 gene alterations occurred more frequently in HPV-negative tumors. HPV-positive tumors were significantly associated with immune signature-related genes compared to HPV-negative tumors. Mutations of NOTCH1 (p=0.027), CDKN2A (p < 0.001), and TP53 (p=0.038) were significantly associated with poorer overall survival. FAT1 mutations were highly enriched in cisplatin responders, and potentially targetable alterations such as PIK3CA E545K and CDKN2A R58X were noted in 14 patients (15%).

conclusionWe found several targetable genetic alterations, and our findings suggest that implementation of precision medicine in HNSCC is feasible. The predictive value of each targetable alteration should be assessed in a future umbrella trial using matched molecular targeted agents.

Indexed as

AdultAgedAged, 80 and overCadherinsClass I Phosphatidylinositol 3-KinasesCyclin D1Cyclin-Dependent Kinase Inhibitor p16Feasibility StudiesFemaleGenetic Predisposition to DiseaseHead and Neck NeoplasmsHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMolecular Targeted TherapyCadherinsCCND1 protein, humanCDKN2A protein, humanClass I Phosphatidylinositol 3-KinasesCyclin D1Cyclin-Dependent Kinase Inhibitor p16FAT1 protein, humanNOTCH1 protein, humanPIK3CA protein, humanReceptor, Notch1TP53 protein, humanTumor Suppressor Protein p53BiomarkersClinical trialMolecular Targeted TherapyNext-generation sequencingSquamous cell carcinoma of the head and neck

Identifiers

PMID29747488
PMCPMC6333965
OpenAlexW2799440650

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.