Evidence map›Paper›PMID 40506495›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2025

[Case Report: Histological Transformation to Atypical Carcinoid in RET Fusion-positive NSCLC Following Immune Therapy Resistance].

Yu Zhang, Hui Zhang, Wei Zhong, Minjiang Chen, Mengzhao Wang

Abstract readCase ReportsEnglish Abstract
In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Yu ZhangDepartment of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, 
Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Hui ZhangDepartment of Pathology, Peking Union Medical College Hospital, 
Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Wei ZhongDepartment of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, 
Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Minjiang ChenDepartment of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, 
Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Mengzhao WangDepartment of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, 
Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) have become the cornerstone of treatment for driver gene-negative advanced non-small cell lung cancer (NSCLC). However, resistance is inevitable, and the underlying mechanisms remain incompletely understood. Histological transformation is a rare but emerging cause of acquired resistance to immunotherapy, with only sporadic case reports documented to date. Here, we report the first case of lung adenocarcinoma that underwent histological transformation to atypical carcinoid following first-line therapy with ICIs combined with chemotherapy, highlighting the critical role of histological lineage switching in mediating NSCLC resistance to ICIs. Notably, the patient harbored a rearranged during transfection (RET) fusion mutation. Subsequent targeted therapy with Selpercatinib after histological transformation demonstrated favorable efficacy, suggesting a potential therapeutic strategy for atypical carcinoid patients with co-occurring rare driver mutations. This case provides a potential therapeutic option for atypical carcinoid patients with rare mutations.
.

Indexed as

Carcinoid TumorCarcinoma, Non-Small-Cell LungDrug Resistance, NeoplasmLung NeoplasmsOncogene Proteins, FusionProto-Oncogene Proteins c-retHumansImmune Checkpoint InhibitorsImmunotherapyImmune Checkpoint InhibitorsOncogene Proteins, FusionProto-Oncogene Proteins c-retRET protein, humanAtypical carcinoidHistological transformationImmune resistanceLung neoplasmsSelective RET inhibitors

Identifiers

PMID40506495
PMCPMC12171582

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.