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Anti-tumor Specific Immune Response in Head and Neck Cancers

Anti-tumor Specific Immune Response in Head and Neck Cancers

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02881918
Acronym
CORISAT
Enrollment
154
Registered
2016-08-29
Start date
2017-03-14
Completion date
2021-03-31
Last updated
2018-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Squamous Cell Carcinoma

Brief summary

The purpose is the description of anti-tumor immune responses in general and according to clinical stage and disease free survival (DFS: survival without recurrence (local or distant)) in patients with Head & Neck Squamous Cell Carcinoma Secondary purposes are: * Study of relationship between anti-tumor immune response and qualitative (yes/no) and quantitative (number) presence of circulating tumor cells (CTCs); * Study of relationship between qualitative (yes/no) and quantitative (number) presence of CTCs and clinical stage as well as DFS * Study of relationship between anti-tumor immune response and clinical stage as well as DFS.

Interventions

OTHERBlood sample

Blood sample with 6 tube of blood (40 mL), after diagnosis and before any specific anticancer treatment

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient with Head & Neck Squamous Cell Carcinoma after extension assessment, regardless of clinical stage (TNM UICC stage I-IV), before any medical or surgical treatment specifically directed against cancer (radiotherapy, surgery, chemotherapy or targeted therapy) * Consent to participate to the study, non-opposition * Affiliation to social security

Exclusion criteria

* History of neoplasia, synchronous cancer, auto-immune disease, organ transplantation, chemotherapy * HIV infection * Corticotherapy during 15 days before blood sampling

Design outcomes

Primary

MeasureTime frame
Presence or absence of spontaneous responses against tumor-associated antigens (TAA) according to tumor stageday 0

Secondary

MeasureTime frameDescription
Functional signature of T cell responses (polyfunctionality index of lymphocytes) according to tumor stageday 0Effector functions and phenotypes of T cells
Number of CTCs according to tumor stageday 0
Polyfunctionality index of lymphocytes according to number of CTCsday 0
Disease free survival (survival without local or distant recurrence) according to Presence pr absence of CTCs at diagnosis2 years after diagnosis
Disease free survival (survival without local or distant recurrence) according to Presence or absence of spontaneous responses against TAA2 years after diagnosis

Countries

France

Contacts

Primary ContactPatrice GALLET
patrice.gallet@yahoo.fr03 83 15 54 17
Backup ContactMarcelo DE CARVALHO

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026