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Single-Cell Transcriptomics of the Peritoneal Microenvironment of Colorectal PC (SingleCell)

G

Ghent University Hospital (UZ)

Status

Enrolling

Conditions

Peritoneal Metastases

Treatments

Procedure: CRC+HIPEC

Study type

Observational

Funder types

Other

Identifiers

NCT05676372
BC-6978

Details and patient eligibility

About

Single cell transcriptomics of CRC PC samples

Full description

Research methodology

Before inclusion of patients, patients will be screened for the presence of hepatitis B, hepatitis C and HIV to ensure researcher safety. During cytoreductive surgery, a total of five samples of tumoral tissue will be acquired. Three of those samples will be utilized for ScRNASeq analysis, and two samples of a macrometastasis will be snap frozen and cryopreserved.

Single-cell RNA-Sequencing analysis We will comprehensively catalog the stromal cell types in the microenvironment of colorectal cancer peritoneal metastases utilizing single-cell RNA sequencing (scRNAseq) on three samples (one of which should preferably originate from the omentum majus, to encompass milky spots) acquired from surgical waste material of patients undergoing cytoreductive surgery. After sample prelevation, samples will be transported as soon as possible while cooled and submerged in 10% PBS to the VIB facilities, where single cell suspensions will be made according to standard protocols. After cell selection by FACS (CD45+ and live/dead stain, to ensure a 50/50 mix of immune and stromal cells) and library prep, ScRNASeq will be performed.

Single cell sequencing analysis will allow us to identify cell clusters that by usage of marker genes will be assigned to different known cell lineages. After annotation of data, a "landscape" of the composition of the tumor stroma will be acquired.

Enrollment

50 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing CRS+HIPEC for PC of colorectal origin

Exclusion criteria

  • Previous HIPEC/PIPAC

Trial contacts and locations

1

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Central trial contact

Wim P Ceelen, MD, PhD; Jesse G Demuytere, MD

Data sourced from clinicaltrials.gov

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