Development of Patient Derived Xenografts (PDXs) and Analysis of Tyrosine Kinase Receptor Expression in Patients With Squamous Cell Head and Neck Cancer (HNSCC) to Study Resistance Mechanisms Induced by Standard Therapy

1. Protocol Identification & Administrative StatusStudy Acronym: SPAR Protocol Date: 04-02-2026 Version: 3 (Superseding version 1 from 26/11/2025) Study Duration: 6.5 years total (5 years enrollment/selection, 8-12 months for PDX expansion, 3 months molecular analysis, 2 months data analysis) Principal Investigator: Mattia Lauriola Coordinating Institution: IRCCS Azienda Ospedaliero-Universitaria di Bologna (Policlinico S. Orsola) 2. Scientific Background & RationaleHead and Neck Squamous Cell Carcinoma (HNSCC) remains a global health challenge, representing the seventh most common cancer with approximately 890,000 new cases and 450,000 deaths annually.The Resistance ProblemWhile standard therapies include surgery, chemotherapy, and radiation, recent innovations like PD-1 inhibitors (pembrolizumab, nivolumab) benefit only 20-30% of patients. Cetuximab (CTX), an anti-EGFR monoclonal antibody, is a standard treatment, but acquired resistance is a frequent barrier.The Biological HypothesisResistance is often driven by:RTK Bypass: Activation of alternative receptor tyrosine kinases (RTKs) such as MET, AXL, IGFR1, and MERTK.ERBB Family Interactions: The ERBB family (EGFR, HER2, HER3, HER4) utilizes complex heterodimerization to maintain signaling despite EGFR inhibition.Signaling Pathways: Downstream activation of RAS and PI3K/AKT pathways, as well as alterations in the tumor microenvironment (e.g., cytokines, EMT markers).The SPAR project aims to address this by developing unique Italian Patient-Derived Xenograft (PDX) models to study these specific resistance mechanisms.3. Study Objectives & OutcomesPrimary ObjectiveGoal: To develop a set of HNSCC PDX models.Method: Implantation of surgical tumor samples into immunocompromised mice.Assessment: Success is evaluated 2-3 months post-implantation.Secondary ObjectivesMolecular Characterization: Comprehensive analysis of RTK expression (EGFR, HER2, HER3, HER4, MET, AXL, IGFR1, MERTK) and their ligands (e.g., NRG1-4, EGF, HGF).Technological Scope: Utilize NGS (genomic and transcriptomic), RT-qPCR, ddPCR, ELISA, Western Blot, and QF-Pro Technology to map the tumor landscape.Virology: Detection of HPV genotypes and presence of viral oncogene transcripts (E6).4. Study Design & MethodologyThis is a non-profit, observational, cross-sectional study using both retrospective and prospective cohorts.Retrospective Phase (n = 40)Sample Source: Archived FFPE (formalin-fixed paraffin-embedded) materials from the last 10 years at IRCCS AOU Bologna.Population: Patients treated with Cetuximab (both locally advanced and R/M settings).Inclusion: Patients must have adequate biological material for immunohistochemical/molecular analysis.Prospective Phase (n = 80)Duration: Enrollment over 5 years.Source: Patients undergoing surgery for HNSCC at IRCCS S. Orsola.PDX Development: Fresh tumor/blood samples collected during standard care.Feasibility: Researchers estimate a 30% success rate for PDX development, targeting sufficient models for a robust biobank.5. Clinical Procedures & Data ManagementClinical EvaluationThis study does not introduce experimental pharmacological treatments; it aligns with the patient's "usual care".Patients in therapy are seen every 2-3 weeks; patients not in active therapy are followed up every 3 months for the first 2 years, then every 6 months for the next 3 years.Data GovernancePlatform: Data is recorded in a pseudonymized electronic Case Report Form (eCRF) using the REDCap platform.Personnel: The Principal Investigator maintains a delegation log for data management duties.Statistical Analysis: Conducted using GraphPad Prism (v.9.5.0). Demographics are reported as frequencies (categorical) or mean/median (continuous).6. Ethics & Regulatory ComplianceInformed ConsentWritten informed consent is mandatory for participation.Special Case (Deceased/Unreachable Patients): For the retrospective cohort, if patients are deceased or unreachable despite reasonable efforts, researchers may proceed without explicit consent under Art. 110, D.Lgs 196/2003, provided they comply with the Italian Data Protection Authority's requirements.Insurance & AmendmentsAs an observational study, no study-specific insurance is required.Any protocol changes must be submitted to the Ethics Committee as formal amendments.7. Dissemination & ReproducibilityOpen Science: The study will be registered on platforms such as clinicaltrials.gov or osf.io.Publication: The investigator commits to submitting findings to a peer-reviewed journal within 12 months of study conclusion, regardless of the results.Data Sharing: Anonymous data will be made available only after publication