Anal Intraepithelial Neoplasia and Anal Squamous Cell Carcinoma

Anal Cancer Clinical Trial

Official title:

The Role of Early Diagnosis and Treatment of Anal Intraepithelial Neoplasia in the Prevention of Anal Squamous Cell Carcinoma: Identifying Prognostic Biomarkers.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05835960
• Other study ID #: 234715
• Status: Recruiting
• Start date: April 1, 2019
• Est. completion date: October 1, 2024

Study information

• Verified date: April 2023
• Source: Imperial College London
• Contact: Micol Lupi, BSc, MBBS, MRCS
• Phone: 020 3315 8000
• Email: m.lupi22[@]imperial.ac.uk
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is a study involving exome sequencing and immune profiling of matched tissue and blood samples from patients with both high-grade squamous intraepithelial lesions and anal squamous cell carcinoma. This is a collaborative project between Imperial College London and the Institute of Cancer Research (ICR), investigating the genetic predeterminants for the progression of anal HSIL to SCC as well as the immunogenetic profile of these conditions will be beneficial for risk stratification (with respect to identifying those individuals with anal HSIL most likely to progress to invasive disease), the identification of potential new drug targets and will add to our understanding of how the tumour microenvironment may influence treatment response and disease recurrence of both anal HSIL and SCC.

Description:

Patients, as identified by the colorectal MDT, are approached, and consented for tissue and blood collection on the day of their diagnostic procedure; the plasma and buffy coat are extracted from the EDTA tubes. A tissue biopsy is performed adjacent to the area sampled for diagnosis and flash frozen in liquid nitrogen. Once the diagnosis of anal cancer is confirmed, the FFPE diagnostic tissue, is requested from the Tissue Bank for the study.

The FFPE and the fresh frozen tissue samples are sliced and put on slides. Stained slides are reviewed by a consultant histopathologist, areas of anal HSIL and SCC are marked.

All samples are transferred to the ICR. Tumour DNA and RNA are extracted from the tissue samples and germline DNA from the buffy coat of the blood sample.

Exome sequencing followed by Bioinformatic analysis is carried out where somatic mutations are evaluated for impact on gene expression and compared between germline, anal HSIL and SCC samples. After a quality control process is complete, the entire dataset is compared with the germline DNA reads, thereby identifying somatic mutations. Candidate mutations are finally cross-referenced with the Cancer Genome Census and string analysis of relevant mutations is performed to assess for cancerogenic impact.

Bulk RNA and targeted RNA based T-Cell Receptor (TCR) sequencing will be carried out, with TCR sequencing also being performed on the blood. This will establish which immune cell types are present in the SCC vs HSIL (by transcriptomic deconvolution), and the repertoire of TCR in peripheral blood, HSIL and SCC. Multiplex immunofluorescence technology against distinct immune panels (established within the CTI), will further evaluate the SCC and HSIL immune microenvironments.

The immune-data will be linked to clinical outcome (both radiological and clinical), following radical chemoradiation.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: October 1, 2024
• Est. primary completion date: April 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

Males or females, with or without HIV over the age of 18 years at the time of recruitment.

Patients with either:

• A previous complete set of formalin fixed tissue samples of all stages of AIN and anal SCC.

• A new diagnosis of AIN3 and are about to undergo Anal mapping.

• A new diagnosis of Anal Squamous Cell Carcinoma and are about to undergo an Examination under Anaesthetic.

Exclusion Criteria:

• Patients without mental capacity to consent.

• Patients less than 18 years old.

• Patients with anal pathology which is not HPV driven AIN/SCC.

Related Conditions & MeSH terms

• Anal Cancer
• Anal Squamous Intraepithelial Neoplasia
• Anus Neoplasms
• Carcinoma in Situ
• Carcinoma, Squamous Cell
• Neoplasms

Locations

Country	Name	City	State
United Kingdom	Imperial College London- Chelsea and Westminster NHS Foundation Trust	London

Sponsors (1)

Lead Sponsor	Collaborator
Imperial College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Identify prognostic biomarkers with respect to anal SCC disease progression and treatment response.	Genomic and immune biomarkers	1 year
Primary	Establish the feasibility of immune analysis and NGS in informing patient treatment decisions.	Pilot study, with low patient numbers	1 year