Study of Specific CD4 Tumors Th1 Responses in Renal Transplant After Occurrence of Cancer

NCT ID: NCT02843763

Last Updated: 2022-08-02

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-07-13
• Study Completion Date: 2022-09-30

Brief Summary

As early complications of transplantation (acute rejection and infections) were better controlled and that the survival of kidney transplants has increased, chronic complications of immunosuppression became increasing challenges. The incidence of cancer is greatly increased in transplant and cancer is now the first cause of death. The iatrogenic immunosuppression plays a major role in the increased incidence of cancer. If it is accepted that the incidence of cancer is generally increased after transplantation, the increased risk is very different from a specific cancer to another. Furthermore the specific treatment of the tumor (surgery, radiotherapy, chemotherapy, biotherapy), the specificity of the context of transplantation is related to the possibility of modulation of immunosuppression. However, there is no immunological marker for predicting the effectiveness of a modification of the immunosuppression.

Several studies point to the important role of CD4 T cells into Th1 anti-tumor immunosurveillance group cancers. Identified "helper" degenerate peptides, called Universal Cancer Peptide (UCP) derivative of telomerase, a type of tumor antigen universal. These UCP peptides bind most HLA-DR alleles most frequent of the population and have the particularity of specifically stimulate CD4 T cells of type Th1. Using a test based on the UCP, it possible to detect the presence of spontaneous CD4 Th1 anti-UCP answers in several types of human cancers.

The main objective of this study is to determine whether, in renal transplant patients, the occurrence of cancer is associated with a deficiency of CD4 Th1 response anti-hTERT.

Conditions

Disorder Related to Renal Transplantation; Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SCREENING
• Blinding Strategy: NONE

Study Groups

Renal transplant with 1rst cancer

Renal transplant patients with first cancer (all cancer excepting skin cancer including in group 2).

Intervention : blood sample

Group Type: OTHER

Blood sample

Intervention Type: OTHER

Blood sample (28 ml)

Renal transplant patients without cancer

Renal transplant patients without cancer matched for age, transplantation duration and CMV/EBV status.

Intervention : blood sample

Group Type: OTHER

Blood sample

Intervention Type: OTHER

Blood sample (28 ml)

Patient with cancer

Patient with cancer from oncology departement matched for cancer type and stade and CMV/EBV status.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Renal transplant with first skin cancer

Renal transplant patients with first epidermoid skin cancer. Intervention : blood sample

Group Type: OTHER

Blood sample

Intervention Type: OTHER

Blood sample (28 ml)

RT with several skin cancer

Renal transplant patients with several epidermoid skin cancer. Intervention : blood sample

Group Type: OTHER

Blood sample

Intervention Type: OTHER

Blood sample (28 ml)

Rt patients without cancer apparied to RT skin cancer

Renal transplant patients without cancer matched for age, transplantation duration and CMV/EBV status with renal transplant patients with skin cancer.

Intervention : blood sample

Group Type: OTHER

Blood sample

Intervention Type: OTHER

Blood sample (28 ml)

Interventions

Blood sample

Blood sample (28 ml)

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Men and women aged 18 to 80 years included
• Signature of informed consent for participation indicating that the subject has understood the purpose and procedures required by the study and agrees to participate in the study and comply with the requirements and limitations inherent in this study
• Join a French social security or receiving such a plan
• Group 1A: renal transplant patients reporting a first cancer (all types of cancer except skin inclued in group 2A or 2B)
• Group 1B: renal transplant patients without cancer (matched to patients in group 1A)
• 1C Group: Non transplant patients reporting a first cancer (patients matched to Group 1A for the type and stage of cancer and the status CMV / EBV)
• Group 2A: kidney transplant patients reporting a single squamous cell carcinoma
• Group 2B: kidney transplant patients with multiple recurrences of squamous cell carcinomas.
• Group 2C: renal transplant patients without cancer (matched to patients in group 2A and 2B)

Exclusion Criteria

• Legal incapacity or limited legal capacity
• Topic unlikely to cooperate in the study and / or low early cooperation by the investigator
• Without health insurance Topic
• Pregnant woman
• Inability to understand the reasons for the study; psychiatric disorders judged by the investigator to be incompatible with the inclusion in the study
• Active infection or not by HIV

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Lille

OTHER

Sponsor Role: collaborator

University Hospital, Tours

OTHER

Sponsor Role: collaborator

Centre Hospitalier Universitaire de Besancon

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Didier Ducloux, Pr.

Role: PRINCIPAL_INVESTIGATOR

Besancon University Hospital, Nephrology department

Locations

Besançon University Hospital

Besançon, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Emilie Gaiffe, Dr.

Role: CONTACT

egaiffe@chu-besancon.fr

0381218824 ext. +33

Ingrid Tissot

Role: CONTACT

itissot@chu-besancon.fr

0381218427 ext. +33

Facility Contacts

Emilie Gaiffe, Dr.

Role: primary

egaiffe@chu-besancon.fr

0381218824 ext. +33

Ingrid Tissot

Role: backup

itissot@chu-besancon.fr

0381218427 ext. +33

Other Identifiers

API/2015/59

Identifier Type: -

Identifier Source: org_study_id