ReviewNaunyn-Schmiedeberg's archives of pharmacology2026
EGFR-targeted tyrosine kinase inhibitors: advancements in cancer therapy.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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.
Who cites it
3 citing papers in PubMed.
- Enhancing EGFR Inhibition: Monensin and Erlotinib Synergize to Eliminate Cancer Stem Cells in Canine Mammary Tumours.Veterinary and comparative oncology · 2026Article
- Does the ERBB/EGF Signaling Network Serve as a Nexus for Oncogenic Signals in Uveal Melanoma?Biomolecules · 2026Review
- Prognostic factors analysis of surgical resection after conversion therapy for isolated pleural metastatic lung cancer: a retrospective analysis.Frontiers in medicine · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cancer treatment has changed significantly with the advent of EGFR-targeted TK inhibitors (TKIs), especially for non-small cell lung cancer (NSCLC). Despite their effectiveness, problems including acquired resistance, particularly the T790M mutation, and non-specific toxicity still exist. Recent developments in drug delivery, combination therapy, and knowledge of resistance mechanisms are addressing these issues. The efficacy of EGFR-targeted therapy has been demonstrated in a wide range of cancers, including head and neck and colorectal cancers. Genomic profiling informs precision medicine, which improves treatment approaches. Targeted cancer therapies, including kinase inhibitors and monoclonal antibodies, block specific signaling pathways essential for tumor growth, offering a more precise alternative to traditional chemotherapy. Moreover, nanotechnology enhances drug delivery, reduces toxicity, and overcomes resistance through advanced nanoparticles like polymeric micelles, PLGA, and chitosan, improving solubility, bioavailability, and sustained EGFR TKI release. This review discusses EGFR's significance in cancer therapy, the evolution of EGFR-targeted TKIs, resistance challenges, and advancements in nanotechnology-based drug delivery. We explore how polymeric and inorganic nanoparticles improve pharmacokinetics and targeted delivery, offering promising solutions to overcome resistance and enhance the therapeutic potential of EGFR-targeted therapies in personalized oncology.
Indexed as
Identifiers
41143954What OpenQuestion holds
Registered trials
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.