Evidence map›Paper›PMID 42266662›Full record

ArticleFrontiers in oncology2026

Case report: complete pathologic response to neoadjuvant ensartinib in locally advanced, ALK-positive lung squamous cell carcinoma.

Yingyu Yang, Junkai Zhang, Zhirun Xie, Sirui Zhang

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2026. 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
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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

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

4 authors.

Yingyu YangDepartment of Pulmonary Oncology, Zhongshan City People's Hospital, Zhongshan, China.
Junkai ZhangDepartment of Pulmonary Oncology, Zhongshan City People's Hospital, Zhongshan, China.
Zhirun XieLiaoning University of Traditional Chinese Medicine Xinglin College, Shenyang, China.
Sirui ZhangBeijing University of Chinese Medicine DongFang College, Cangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ALK-positive of anaplastic lymphoma kinase (ALK) is rare in lung squamous cell carcinoma (LSCC), with an incidence of less than 1%. The role of neoadjuvant treatment with ALK inhibitors remains understudied. Here, we report the first case of stage IIIB, ALK-positive LSCC that achieved complete pathologic responses (pCR) to neoadjuvant ensartinib. In the current study, EML4-ALK positivity was identified by next-generation sequencing in a case with locally SCC. Rapid partial response was observed after four weeks of ensartinib. The patient continued to receive 6 weeks of ensartinib followed by right upper lobectomy with complete pathological response. To the best of our knowledge, limited data are available regarding the role of ensartinib as a neoadjuvant therapy for ALK-positive, non-small cell lung cancer (NSCLC) patients. Our case provided evidence that locally advanced, ALK-positive LSCC could benefit from neoadjuvant ensartinib, with an impressive response and favorable safety. Our findings may also extend the indications for targeted therapy to the neoadjuvant setting in locally advanced, ALK-positive, resectable LSCC.

Indexed as

ALKcase reportensartiniblung cancerlung squamous cell carcinoma

Identifiers

PMID42266662
PMCPMC13243048

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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.