Evidence map›Paper›PMID 33273725›Full record

ArticleOncogene2021

Genomic origin and intratumor heterogeneity revealed by sequencing on carcinomatous and sarcomatous components of pulmonary sarcomatoid carcinoma.

Xuewen Liu, Fang Wang, Chunwei Xu, Xinru Chen, Xue Hou, Qian Li, Pansong Li, Zhi Xie, Yongdong Liu, Lianpeng Chang and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Article
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  5. Distinct Clinicogenomic Features and Immunotherapy Associations in Pulmonary Sarcomatoid Carcinoma: A Multicenter Retrospective Study.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Article
  6. Article
  7. Article
  8. Article
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  10. Review
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  14. Review
  15. Targeted therapy for rare lung cancers: Status, challenges, and prospects.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
  16. Article
  17. Article
  18. Review
  19. Comprehensive analysis ofTherapeutic advances in medical oncology · 2022
    Article
  20. Article
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

19 authors at 6 institutions in 2 countries.

Xuewen Liu *Department of Oncology, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, P.R. China.
Fang Wang *Department of Molecular Diagnostic, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, Guangdong, P. R. China.
Chunwei Xu *Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, Jiangsu, P.R. China.
Xinru Chen *Department of Medical Oncology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, Guangdong, P. R. China.
Xue Hou *Department of Medical Oncology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, Guangdong, P. R. China.
Qian LiGeneplus-Beijing, Beijing, 102206, P. R. China.ORCID http://orcid.org/0000-0001-9413-1877
Pansong LiGeneplus-Beijing, Beijing, 102206, P. R. China.
Zhi XieGuangdong Lung Cancer Institute, Guangdong Provincial Key Laboratory of Translational Medicine in Lung Cancer, Guangdong General Hospital (GGH) and Guangdong Academy of Medical Sciences, Guangzhou, 510080, Guangdong, P. R. China.
Yongdong LiuDepartment of Pathology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, Guangdong, P. R. China.
Lianpeng ChangGeneplus-Beijing, Beijing, 102206, P. R. China.
Yanfang GuanGeneplus-Beijing, Beijing, 102206, P. R. China.
Xuchao ZhangGuangdong Lung Cancer Institute, Guangdong Provincial Key Laboratory of Translational Medicine in Lung Cancer, Guangdong General Hospital (GGH) and Guangdong Academy of Medical Sciences, Guangzhou, 510080, Guangdong, P. R. China.
Ling YangGeneplus-Beijing, Beijing, 102206, P. R. China.
Hui WangDepartment of Radiation Oncology, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University; Hunan Provincial Key Laboratory of Translational Radiation Oncology, Changsha, 410013, Hunan, P. R. China.
Xin YiGeneplus-Beijing, Beijing, 102206, P. R. China.
Jianjun ZhangDepartment of Genomic Medicine and Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA.
Xuefeng XiaGeneplus-Beijing, Beijing, 102206, P. R. China.
Cesar MoranDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, 77030, TX, USA. cesarmoran@mdanderson.org.ORCID http://orcid.org/0000-0003-1158-5713
Likun ChenDepartment of Medical Oncology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, Guangdong, P. R. China. chenlk@sysucc.org.cn.ORCID http://orcid.org/0000-0002-7158-3878
Annoroad Gene Technology (China) · CNSun Yat-sen University · CNCentral South University · CNGuangdong General Hospital · CNThe University of Texas MD Anderson Cancer Center · USNanjing General Hospital of Nanjing Military Command · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary sarcomatoid carcinoma (PSC) contains carcinomatous component (CaC) and sarcomatous component (SaC). Herein, we explored the genomic origin and intratumor heterogeneity (ITH) of PSC. We collected 31 resected PSC tumors and obtained CaC and SaC by laser capture microdissection for next-generation sequencing. The majority of PSCs (97%) had component-shared alterations. Driver mutations in EGFR, KRAS, MET, PIK3CA, and EML4-ALK fusion were mostly component-shared. Twenty-seven (87%) PSCs had component-private alterations. Compared with pure lung adenocarcinoma (LUAD), adenocarcinoma component of PSC showed lower EGFR incidence. Compared with other typical sarcomas, numerous genes of SaC exhibited significant differences. CaC and SaC had equivalent and proportional tumor mutation burden (TMB), as well as PD-L1 level. Compared with LUAD, SaC had significant higher TMB and more patients with high PD-L1 expression (tumor proportion score ≥50%). PSC with lower proportion of component-shared alterations (trunk-ratio) had a prolonged disease-free survival (DFS), regardless of the influence of clinical factors. We conclude that most PSCs originate from a monoclone accompanied by genomic ITH which is a potential independent prognostic factor, and more proportion of PSCs may be beneficial from immune checkpoint inhibitors.

Indexed as

AdultAgedAged, 80 and overB7-H1 AntigenCarcinoma, Non-Small-Cell LungFemaleGenomicsHigh-Throughput Nucleotide SequencingHumansLaser Capture MicrodissectionLung NeoplasmsMaleMiddle AgedMutationSarcomaB7-H1 Antigen

Identifiers

PMID33273725
OpenAlexW3106670734

What OpenQuestion holds

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Registered trials

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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.