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Adenocarcinoma of the ampulla of Vater (AAC) is a rare malignancy with heterogeneous tumors arising from various histologic subtypes, necessitating new therapeutic strategies. This study examines epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and c-Met expression in AAC, given their potential as druggable targets. Among 87 patients who underwent curative resection, EGFR overexpression was found in 87.4%, HER2 in 11.5%, and c-Met in 50%. EGFR overexpression was more common in the pancreatobiliary subtype ( = 0.018) and associated with a higher histologic grade ( = 0.008). HER2 did not correlate with clinicopathological features, while c-Met was more common in node-negative groups ( = 0.004) and often co-expressed with EGFR ( = 0.049). EGFR-positive patients had worse disease-free (HR = 2.89; 95% CI, 1.35-6.20; = 0.061) and overall survival (HR = 6.89; 95% CI, 2.94-16.2; = 0.026) than EGFR-negative patients. HER2-positive AAC showed a trend towards shorter survival, although not statistically significant, and c-Met had no impact on survival outcomes. In the context of systemic disease, survival outcomes did not vary according to EGFR, HER2, and c-Met expression, but the HER2-positive group showed a trend towards inferior progression-free survival (HR = 1.90; 95% CI, 0.56-6.41; = 0.166). This study underscores the potential of EGFR, HER2, and c-Met as targets for personalized therapy in AAC, warranting further research to evaluate targeted treatments.
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http://dx.doi.org/10.3390/cancers16152756 | DOI Listing |
Adv Sci (Weinh)
August 2025
Department of Pharmacy, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Osimertinib resistance is a global problem for NSCLC patients mediated by new EGFR mutations or bypass mechanisms. Proteolysis targeting chimeras (PROTACs) have been utilized to overcome drug resistance by degrading mutant EGFR, but most are restricted to their poor cell permeability and insufficient tumor-targeting ability. Meanwhile, these PROTACs has little effect on bypass resistance mechanisms.
View Article and Find Full Text PDFJ Med Chem
July 2025
National Engineering Research Center for Strategic Drugs, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.
The cellular-mesenchymal epithelial transition factor (c-Met) is an attractive target in multiple cancers. Despite various c-Met inhibitors having been developed, the acquired drug resistance hampers their clinical application. In this study, through elaborately rational optimization, c-Met degraders, namely, , , and , were developed to exhibit single-digit nanomolar cell growth inhibition IC values, picomolar c-Met degradation DC values, and >99% of maximum degradation in cancer cells with alterations via a Cullin-CRBN-dependent pathway.
View Article and Find Full Text PDFMikrochim Acta
June 2025
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif, 21944, Saudi Arabia.
Cancer is a significant global health concern, with its prevalence continuing to rise steadily. Early detection is vital for improving treatment outcomes and survival rates by enabling timely intervention and effective disease management. Biosensors have emerged as crucial tools in cancer diagnosis, offering high sensitivity, selectivity, and rapid detection of biomarkers.
View Article and Find Full Text PDFJAMA Oncol
July 2025
Department of Medical Oncology, Gustave Roussy, International Center for Thoracic Cancers, Villejuif, France.
Importance: Patients with advanced RET fusion-positive (RET+) non-small cell lung cancer (NSCLC) who experience disease progression following treatment with RET inhibitors (RETis) have limited treatment options. Identifying membrane protein targets may support the assessment of novel therapies, such as antibody-drug conjugates and bispecific antibodies.
Objective: To evaluate membrane target expression in RET+ NSCLC.
Pharmaceutics
May 2025
Clinical Pharmacy Service, Mediterranean Institute for Transplantation and Advanced Specialized Therapies (IRCCS ISMETT), Via Ernesto Tricomi, 5, 90127 Palermo, Italy.
: Lung cancer is the leading cause of cancer-related deaths worldwide. Non-Small-Cell Lung Cancer (NSCLC) accounts for 80-90% of all lung cancers. Antibody-Drug Conjugates (ADCs) represent an expanding targeted therapy option for the treatment of NSCLC.
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