Clinical trial · Interventional
Study of Genetic and Cellular Immunological Parameters Predictive of Disease-free Survival in Patients With Metastatic Cancer
NCT02838381CI-TRIAL-00084088Epitopes-CRC01completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim of this study is to characterize the genetic and cellular immunological parameters of metastatic digestive cancer patients having short and long responses to chemotherapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Metastatic Cancer | Malignant Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Additional biological samples | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Additional biological samples
- description
- Additional blood samples will be realized at the inclusion of patients. Two optional blood samples could be realized if necessary with at least 3 months apart. Peripheral Blood Mononuclear Cells (PBMC) will be collected. Tissue tumor will be collected if available.
- interventionNames
- Other: Additional biological samples
Primary outcomes (2)
- measure
- frequency of peripheral T cell immune responses in the presence of antigenic peptides associated with digestive cancer
- timeFrame
- at inclusion
- measure
- progression-free survival
- timeFrame
- within 5 years after the inclusion
- description
- time interval between the date of inclusion and the date of first progression or death from any cause.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: For all patients: * signed written informed consent For cohort A: * patient with metastatic colorectal cancer with first-line therapy by chemotherapy +/- surgery and with a disease-free survival \> or = at 20 months * Ct-scan realized in the previous 4 weeks and showing no progression according to the Recist criteria v1.1 For cohort B: * patient treated for metastatic colorectal cancer and chemotherapy responder (obtention of an objective response according to the Recist criteria V1.1 in first-line therapy), with a disease-free survival \< 10 months (disease progression must be confirmed by CT scan evaluation according to Recist v1.1 criteria) For cohort C: * patients with no metastatic rectum cancer in complete remission after chemotherapy and/or radiotherapy For cohort D: * patients with metastatic or locally advanced cancer in complete remission after treatment, non eligible in the other cohorts Exclusion Criteria: For all patients: * patient with any medical or psychiatric condition or disease which would make the patient inappropriate for entry into this study * patient with a neurodegenerative disease * patient under guardianship, curator or under the protection of justice
References
Publications (1)
- DERIVEDLopez M, Spehner L, Andre F, Viot J, Seffar E, Marguier A, Curtit E, Meynard G, Dobi E, Ladoire S, Boidot R, Loyon R, Derangere V, Bidard FC, Borg C, Mansi L, Kroemer M. Exploring the role of ESR1 mutations in metastatic hormone receptor-positive breast cancer T cell immune surveillance disruption. Breast Cancer Res. 2025 Feb 7;27(1):19. doi: 10.1186/s13058-025-01962-6. PMID 39920833