Study of the Contribution of Mutant p53/YAP Proteins to Therapy Resistance in Recurrent Head and Neck Cancer

Multicenter, non-interventional, retrospective/prospective study of a biological nature, on patients affected by head and neck tumors, for which the collection and use of tissue samples is planned for the study of the mutational profile, the transcriptional profile and the proteomic profile.

Study Overview

• Status: Recruiting
• Conditions: Head and Neck Tumors
• Intervention / Treatment: Biological: Culture of organoids

Detailed Description

The study aims to characterize molecular networks governed by the mutated protein p53 with a relevant role in the development of local recurrence in head and neck tumors HNSCC, in order to identify the main actors involved in resistance to current therapy and try to develop new more effective therapeutic strategies for head and neck tumors.

Furthermore, the existence of a significant relationship between the time of onset of recurrence and the deregulation of the identified molecular networks will be studied.

This study will therefore allow to:

1. Identify networks associated with the presence of mutation in the TP53 gene relevant in the development of relapse, comparing the tissues of the primary tumor to the respective tissue of the relapse of patients affected by head and neck cancer, by:

   1. expression profiles of coding and non-coding RNAs (retrospective cohort)
   2. mutational profile by NGS (retrospective cohort)
   3. Single cell RNA-sequencing (SC-RNAseq) on samples belonging to the prospective cohort
2. Characterize the molecular mechanisms underlying TP53-dependent networks with a key role in resistance to therapy, using resistance cell systems and in organoid cultures derived from head and neck tumors HNSCC (PDO) (prospective cohort).
3. Identify the best treatment combinations able to target the networks identified as associated with resistance (prospective cohort).
4. To evaluate the response of treatments in vivo using a syngeneic model of head and neck tumors HNSCC (MOC model).

• Study Type: Observational
• Enrollment (Estimated): 18

Contacts and Locations

• Study Contact: Name: Giovanni Blandino, Doctor; Phone Number: +39 06 52662911; Email: giovanni.balndino@ifo.it

Study Locations

• Italy
  • Rome
    • Roma, Rome, Italy, 00144
      • Recruiting
      • IRCCS National Cancer Institute
      • Contact: Giovanni Blandino, Doctor; Phone Number: +39 06 52662911; Email: giovanni.blandino@ifo.it

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

Patients with head and neck tumors

Description

Inclusion Criteria:

• Age over 18
• Patients with squamous cell tumors of the oral cavity, pharynx or larynx
• Surgical patients with primary HNSCC tumors, who have not had previous tumors in other sites or adjuvant treatments prior to surgery.
• Availability of adequate material (tissue) for the planned analyses
• Availability of follow-up data for at least one year (retrospective part)
• Written informed consent (prospective part and/or, for the retrospective part, traceable patients and/or patients in follow-up and/or if necessary for the legal nature/institutional purposes of the participating centers).

Exclusion Criteria:

• Presence of distant metastases at the time of diagnosis
• Previous head and neck cancer
• Second cancer undergoing treatment or follow-up for less than 5 years

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Organoids cultures	Fresh tissue samples collected from surgery at the reference centers will be selected by the pathologist, and stored at 4°C in special media at the reference laboratories. These samples will be evaluated by means of viabilityassays with ATPlite, the ability to form colonies and apoptosis assays (by FACS). For organoids, the response to treatment will be performed by macroscopic analysis, evaluating the size and number of organoids before and after treatment.	60 months

Collaborators and Investigators

• Sponsor: Regina Elena Cancer Institute
• Investigators: Principal Investigator: Giovanni Blandino, Doctor, IRCCS National Cancer Institute

Study record dates

Study Major Dates

• Study Start (Actual): March 7, 2024
• Primary Completion (Estimated): March 7, 2029
• Study Completion (Estimated): March 7, 2029

Study Registration Dates

• First Submitted: January 16, 2025
• First Submitted That Met QC Criteria: January 23, 2025
• First Posted (Actual): March 25, 2025

Study Record Updates

• Last Update Posted (Actual): March 25, 2025
• Last Update Submitted That Met QC Criteria: January 23, 2025
• Last Verified: January 1, 2025

More Information

Terms related to this study

• Keywords: TP53; organoids; head and neck tumors
• Additional Relevant MeSH Terms: Neoplasms by Site; Neoplasms; Head and Neck Neoplasms
• Other Study ID Numbers: RS105/IRE/24

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No