Evidence map›Paper›PMID 40703207›Full record

ArticleOncoTargets and therapy2025

A Rare Histologic Transformation from EGFR-Positive Lung Adenocarcinoma to EGFR-Negative Squamous Cell Carcinoma After EGFR-TKIs Resistance: A Case Report.

Mengli Qiu, Peiwen Guo, Jieheng Lin, Sisi Wang, Wenping Wang, Jianying Yang, Zhongming Huang, Yang Cao

Abstract readCase Reports
In one paragraph

Article in OncoTargets and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

Mengli QiuThe First Clinical School, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.
Peiwen GuoThe First Clinical School, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.
Jieheng LinDepartment of Oncology, The First Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.
Sisi WangDepartment of Oncology, The First Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.
Wenping WangDepartment of Oncology, The First Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.ORCID 0000-0002-1851-5219
Jianying YangDepartment of Oncology, The 928rd Hospital of the Chinese People's Liberation Army Joint Logistic Support Force, Haikou, People's Republic of China.
Zhongming HuangDepartment of Oncology, Cancer Hospital of Shantou University Medical College, Shantou University, Shantou, People's Republic of China.
Yang CaoDepartment of Oncology, The First Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung adenocarcinoma (ADC) harboring epidermal growth factor receptor (EGFR) mutations rarely transforms into squamous cell carcinoma (SCC) following resistance to targeted therapy. Here, we present a case of EGFR-positive ADC that transformed into EGFR-negative SCC after developing resistance to EGFR tyrosine kinase inhibitors (TKIs). The patient experienced progressive disease after one cycle of chemotherapy and subsequently underwent five courses of tislelizumab combined with chemotherapy. Although the primary tumor showed a partial response to this combined regimen, intracranial metastases continued to progress, ultimately leading to the patient's death. Notably, the patient survived for 8 months after SCC transformation with immuno-chemotherapy, a significantly longer duration than the previously reported median survival of 3.5 months. This case underscores the occurrence of genomic instability, histological transformation, and dissociated response (DR) following treatment with EGFR-TKIs in EGFR-positive lung ADC. We hypothesize that these phenomena may be driven by tumor heterogeneity and the dynamic variability within the tumor microenvironment (TME).

Indexed as

brain metastaseschemotherapydissociated responseepidermal growth factor receptorhistological transformationimmunotherapy

Identifiers

PMID40703207
PMCPMC12283237

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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.