Evidence map›Paper›PMID 41158851›Full record

ArticleFrontiers in oncology2025

Durable clinical benefit from gefitinib plus bevacizumab in a non-small cell lung cancer patient with an acquired C797S mutation following osimertinib treatment: a case report and literature review.

Yuping Tan, Meng Dong, Xi Li, Wenbo Li, Fei Xiong, Weidong Bao, Yongzhou Dai, Linjun Yue, Yuan Liu

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Yuping Tan *Department of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Meng Dong *Department of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Xi LiDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Wenbo LiDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Fei XiongDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Weidong BaoDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Yongzhou DaiDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Linjun YueDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Yuan LiuDepartment of Interventional Oncology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The emergence of the epidermal growth factor receptor (EGFR) C797S mutation in the absence of T790M represents a common mechanism of acquired resistance to first-line osimertinib in non-small cell lung cancer (NSCLC), posing a significant clinical challenge. Case presentation: We present the case of a 72-year-old man diagnosed with metastatic NSCLC harboring an EGFR exon 19 deletion who developed an acquired C797S mutation (without T790M) following 25 months of first-line osimertinib therapy. Based on this molecular profile, the patient received a regimen of gefitinib combined with bevacizumab. This combination was well tolerated and resulted in a partial response, achieving a progression-free survival (PFS) of 15.5 months. Conclusion: This case indicates that the combination of gefitinib and bevacizumab may offer a durable clinical benefit for NSCLC patients who develop osimertinib resistance via the C797S mutation. The observed outcomes warrant further investigation into this dual-blockade strategy, especially given the limited duration of response noted for tyrosine kinase inhibitor (TKI) monotherapy.

Indexed as

bevacizumabC797S mutationepidermal growth factor receptornon-small-cell lung cancertyrosine kinase inhibitor

Identifiers

PMID41158851
PMCPMC12554549

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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.