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Detection of Circulating Tumor DNA in p16- Locally Advanced Head Neck Squamous Cell Carcinoma (PERSO-NECK)

Primary Purpose

Head and Neck Squamous Cell Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Detecton of circulating tumor DNA
Sponsored by
Centre Henri Becquerel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Head and Neck Squamous Cell Carcinoma focused on measuring circulating tumor DNA, Next Generation Sequencing, Digital PCR

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Operable Head and neck squamous cell carcinoma (T3-T4 stage and/or N+)
  • No p16 expression
  • Curative treatment proposed based on surgery + radiotherapy (+/- chemotherapy)
  • PS<3
  • Written consent signed

Exclusion Criteria:

  • Metastatic spread
  • Previous radiotherapy of head or neck
  • Previous HNSCC (except carcinoma restricted to glottis, with a surgery treatment alone and >3 years of follow up without relapse)

Sites / Locations

  • Centre Henri BecquerelRecruiting
  • CHURecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Detection of circulating tumor DNA

Arm Description

sampling of 20 ml of blood the day before surgery, the day after , 6 months after diagnosis and every 3 months thereafter until 18 months of follow up

Outcomes

Primary Outcome Measures

Percentage of patients with a detectable mutation in ctDNA
number of patient with detectable mutation with personalized molecular probe

Secondary Outcome Measures

Kinetics of ctDNA
Evaluation of the number of patients with an increase or decrease of circulating tumor DNA level
Kinetics of ctDNA in case of relapse
Evaluation of the number of patients with an increase or decrease of circulating tumor DNA level
progression free survival
time between inclusion and progression and correlation with circulating tumor DNA level

Full Information

First Posted
February 5, 2019
Last Updated
July 29, 2020
Sponsor
Centre Henri Becquerel
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1. Study Identification

Unique Protocol Identification Number
NCT03896412
Brief Title
Detection of Circulating Tumor DNA in p16- Locally Advanced Head Neck Squamous Cell Carcinoma
Acronym
PERSO-NECK
Official Title
Detection of Circulating Tumor DNA by a Personalized Molecular Tool During Treatment of Locally Advanced Operable Head and Neck Squamous Cell Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 21, 2019 (Actual)
Primary Completion Date
May 19, 2021 (Anticipated)
Study Completion Date
May 19, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Henri Becquerel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Locally advanced head and neck squamous cell carcinoma (LAHNSCC) is a heterogeneous disease, associated with a poor prognosis and no improvement in overall survival for years. Furthermore, treatments (surgery, radiotherapy, chemotherapy) are frequently associated with acute and late toxicities. Beside p16/HPV + tumors, only TNM classification can help estimating the prognosis of the patients. A better evaluation of the prognosis and of the risk of metastatic spread would help defining the best treatment. Circulating tumor DNA (ctDNA) has been reported as both a prognostic factor and a non-invasive way to assess tumor relapse in several cancer types. Few data are available in HNSCC, and no data among p16/HPV- cancers. Indeed, ctDNA assessment is usually based on tumor mutation monitoring. But if recurrent mutations are frequent in several cancers types (PIK3CA, KRAS, ESR1, TERT…), there is no recurrent mutation observed in HNSCC. Thus ctDNA assessment in LAHNSCC must be performed after the identification of a tumor specific mutation for each patient. In that context, the aim of this study is to perform a molecular analysis of primary LAHNSCC, and to look for the amount of ctDNA before surgery, after surgery, and during 18 months of follow up.
Detailed Description
The patients will be enrolled before surgery and follow-up during 18 months. During patient participation, 20 ml of blood will be collected 7 times (before and after surgery, 6 months after diagnosis and every 3 months thereafter until 18 months of follow up). Mutation analysis on tumor and healthy tissue will be performed on primary tumors and lymph node dissection, after removal by the surgeon. Circulating tumor DNA will be detected on blood sample

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Squamous Cell Carcinoma
Keywords
circulating tumor DNA, Next Generation Sequencing, Digital PCR

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Detection of circulating tumor DNA
Arm Type
Experimental
Arm Description
sampling of 20 ml of blood the day before surgery, the day after , 6 months after diagnosis and every 3 months thereafter until 18 months of follow up
Intervention Type
Other
Intervention Name(s)
Detecton of circulating tumor DNA
Intervention Description
7 blood samples to design a molecular probe
Primary Outcome Measure Information:
Title
Percentage of patients with a detectable mutation in ctDNA
Description
number of patient with detectable mutation with personalized molecular probe
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Kinetics of ctDNA
Description
Evaluation of the number of patients with an increase or decrease of circulating tumor DNA level
Time Frame
18 months
Title
Kinetics of ctDNA in case of relapse
Description
Evaluation of the number of patients with an increase or decrease of circulating tumor DNA level
Time Frame
18 months
Title
progression free survival
Description
time between inclusion and progression and correlation with circulating tumor DNA level
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Operable Head and neck squamous cell carcinoma (T3-T4 stage and/or N+) No p16 expression Curative treatment proposed based on surgery + radiotherapy (+/- chemotherapy) PS<3 Written consent signed Exclusion Criteria: Metastatic spread Previous radiotherapy of head or neck Previous HNSCC (except carcinoma restricted to glottis, with a surgery treatment alone and >3 years of follow up without relapse)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Florian Clatot, MD,PhD
Phone
+33232082231
Email
floriane.clatot@chb.unicancer.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Doriane Richard, PhD
Phone
+33232082985
Email
doriane.richard@chb.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Flrorian Clatot, MD,PhD
Organizational Affiliation
Centre Henri Becquerel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Henri Becquerel
City
Rouen
ZIP/Postal Code
76000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Florian Clatot, Md,PhD
Phone
+33232082231
Email
florian.clatot@chb.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Doriane Richard, PhD
Phone
+33232082985
Email
doriane.richard@chb.unicancer.fr
Facility Name
CHU
City
Rouen
ZIP/Postal Code
76000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicolas Bon Mardion, Md,PhD
Email
nicolas.bon-mardion@chu-rouen.fr

12. IPD Sharing Statement

Learn more about this trial

Detection of Circulating Tumor DNA in p16- Locally Advanced Head Neck Squamous Cell Carcinoma

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