Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06435689

Study and Modulation of Immune Responses in Primary and Metastatic Colon Cancers

Colorectal cancer (CRC) is the 3rd most common cancer in France. Treatment of CRC relies primarily on surgical removal of the primary tumor and chemotherapy is the current standard of care for synchronous metastatic disease. Overall survival remains strongly correlated with the tumor stage at the time of surgery, from 90% at five years for localized disease (stages 1 and 2), to around 20% for metastatic forms of the disease (stage 4). Recent research in cancer highlights the role of the immune system in the development, evolution and fate of tumors. Understanding the nature of interactions between different immune cells infiltrating the tumor is important for the development of innovative therapies. Recently, the consensus molecular classification of CRC confirmed the importance of the immune response in CRC by showing that a "high immune response" is a good prognostic indicator for patients with this pathology. However, immunotherapies are effective for only a minority of patients with metastatic CRC. Indeed, anti Programmed cell Death 1 (anti-PD-1), -PD-L1 immune checkpoint blocking antibodies have only shown effectiveness in patients with microsatellite instability (MSI), which only represents 5% of metastatic CRCs.

Thus, the aim of this study is to better understand the role of the immune system on the development of CRC and its possible modulation to treat or prevent metastatic recurrences.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hôpital Saint Louis - gastoenterology, Paris, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female 18 years of age or older
  • Diagnosis of colorectal adenocarcinoma
  • Scheduled resection of tumor and/or metastasis(es)

Exclusion criteria

  • Patient's opposition to research
  • Patients under guardianship
  • The following situations
  • Persons unable to understand and/or read the information leaflet
  • Patient with one of the following functions: Investigator or co-investigator, research assistant, pharmacist, study coordinator or, having any involvement in the study
  • Non-cooperative or potentially non-compliant person for the study and its procedures with foreseeable difficulties in regular follow-up over 5 years.
  • Non-affiliation with a social security scheme, Couverture Médicale Universelle or any equivalent scheme.
  • Pregnant or breast-feeding women.
  • HIV-positive patients.

Treatment and study plan

Sampling

Other

Blood and surgical specimen sampling the day of surgery

Primary outcomes

  1. Effectiveness of immunotherapies in a co-culture model

    Time frame: At 1 year

    Characterize effective immunotherapies in colorectal cancers by demonstrating their effectiveness in a co-culture model between cancer cells and autologous T cells.

Secondary outcomes

  1. Evaluation of transcriptomic differences

    Time frame: At 5 years

    Evaluation of transcriptomic differences between tissues or cells from the healthy mucosa compared to those from the primary or metastatic tumor: sequencing of mRNA in the two types of mucosa and comparison of mRNA expression profiles between the latter.

  2. Evaluation of proteomic differences

    Time frame: At 5 years

    Evaluation of proteomic differences between tissues or cells from the healthy mucosa in comparison to those from the primary tumor by:

    multiplexed immunodetection in situ in tissues detection and dosage of proteins in culture supernatants (ELISA), in a co-culture model between cancer cells and autologous T cells, with or without modulation of a pathway targeting the T lymphocyte response by immunotherapy.

  3. Evaluation of the T Cell Receptor (TCR) repertoire

    Time frame: At 5 years

    Evaluation of the TCR repertoire by sequencing, carried out from:

    patient blood, DNA from cancerous tissues and healthy mucosa DNA from the co-culture between cancer cells and autologous T cells, with or without modulation of a pathway targeting the T lymphocyte response by immunotherapy

Study contacts

Contact information is provided by the study sponsor or research team.

Jérôme Lambert, Pr

CONTACT

[email protected]

142499742 ext. +33

Thomas Aparicio, Pr

CONTACT

[email protected]

142499597 ext. +33

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Etude et Modulation de la réponse Immunitaire Dans Les Cancers COlorectaux Primaires et METastatiques

Acronym: I-COMET

Important dates

Study start
2024
Primary completion
2025
Study completion
2039
First posted
May 30, 2024
Registry last updated
May 30, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.