Evidence map›Paper›PMID 35144629›Full record

ArticleDiagnostic pathology2022

Pulmonary large cell carcinoma with neuroendocrine morphology shows genetic similarity to large cell neuroendocrine carcinoma.

Zuoyu Liang, Weiya Wang, Qianrong Hu, Ping Zhou, Ying Zhang, Yuan Tang, Qian Wu, Yiyun Fu, Xue Li, Yang Shao and 1 more

Abstract read
In one paragraph

Article in Diagnostic pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

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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

8 citing papers in PubMed.

  1. Article
  2. Frontiers in medicine · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  8. Article
4 · The record

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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

11 authors.

Zuoyu Liang *Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Weiya Wang *Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Qianrong HuWest China School of Medicine, Sichuan University, Chengdu, China.
Ping ZhouDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Ying ZhangDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Yuan TangDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Qian WuDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Yiyun FuDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Xue LiNanjing Geneseeq Technology Inc, Nanjing, China.
Yang ShaoNanjing Geneseeq Technology Inc, Nanjing, China.
Lili JiangDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China. 879876047@qq.com.

Funding

1.3.5 Project for Disciplines of Excellence-Clinical Research Incubation Project, West China Hospital, Sichuan University 2019HXFH002Sichuan Province Science and Technology Support Program 2020YFS0275
6 · The paper itself

Abstract

backgroundLarge cell neuroendocrine carcinoma (LCNEC) is a high-grade malignant pulmonary neuroendocrine tumour. The distinction of pulmonary large cell carcinoma (LCC) and LCNEC is based on the presence of neuroendocrine morphology and the expression of at least one neuroendocrine marker in at least 10% of tumour cells in the latter. According to the current classification, LCC with neuroendocrine morphology and without neuroendocrine marker expression is classified as LCC. This subgroup we have named LCNEC-null and aimed to analyze its characteristics.

methods31 surgical samples resected in West China Hospital of Sichuan University between 2017 to 2021 were collected, including 7 traditional LCCs, 11 LCNEC-nulls and 13 LCNECs. Each case was conducted to immunohistochemistry and 425-panel-NGS.

resultsCompared to other LCCs, detailed analysis of LCNEC-nulls revealed biological features similar to those of LCNECs, especially for immunohistochemistry and molecular analysis: 1. diffusive, coarse granular and high expression of Pan-CK; 2. rare PD-L1 expression; 3. High rate of p53 expression and Rb deficiency 4. abundant genetic alterations are similar to LCNEC. All characteristics above deviated from traditional LCC, indicating they have the same origin as LCNEC. Furthermore, LCNEC could be genetically divided into two subtypes when we reclassified LCNEC-null as LCNEC, and the mutational type and prognosis differed significantly.

conclusionsWe consider that LCNEC-null should be reclassified as LCNEC based on analysis above. In addition, two genetic types of LCNEC with different prognosis also indicate two mechanism of tumour formation.

Indexed as

Carcinoma, Large CellCarcinoma, NeuroendocrineLung NeoplasmsHumansImmunohistochemistryPrognosisLarge cell carcinomaLarge cell carcinoma with neuroendocrine morphologyLarge cell neuroendocrine carcinomaTP53

Identifiers

PMID35144629
PMCPMC8832809

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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.