Anal Intraepithelial Neoplasia and Anal Squamous Cell Carcinoma

Trial Title: Anal Intraepithelial Neoplasia and Anal Squamous Cell Carcinoma

NCT ID: NCT05835960

Condition: Anal Cancer
Anal Squamous Intraepithelial Neoplasia

Conditions: Official terms:
Carcinoma, Squamous Cell
Neoplasms
Carcinoma in Situ
Anus Neoplasms

Conditions: Keywords:
Anal Cancer
Early Diagnosis
Anal Squamous Intraepithelial Lesion
Biomarker
HPV
Treatment response

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Prospective

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.

Detailed 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.

Criteria for eligibility:

Study pop:
Patients with HPV driven AIN 3 and anal SCC.

Sampling method: Non-Probability Sample
Criteria:
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.

Gender: All

Minimum age: N/A

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Imperial College London- Chelsea and Westminster NHS Foundation Trust

Address:
City: London
Zip: SW10 9NH
Country: United Kingdom

Status: Recruiting

Contact:
Last name: Micol Lupi

Phone: 020 3315 8000

Phone ext: 4469
Email: m.lupi22@imperial.ac.uk

Contact backup:
Last name: Christos Kontovounisios

Phone: 020 3315 8000

Phone ext: 4469
Email: c.kontovounisios@imperial.ac.uk

Investigator:
Last name: Christos Kontovounisios
Email: Principal Investigator

Investigator:
Last name: Paris Tekkis
Email: Principal Investigator

Start date: April 1, 2019

Completion date: October 1, 2024

Lead sponsor:
Agency: Imperial College London
Agency class: Other

Source: Imperial College London

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05835960