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Study of Circulating Markers in Serum of Patients Treated for Metastatic Colorectal Cancer (Coca-Colon)

Primary Purpose

Metastatic Colorectal Cancer

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Blood sampling
Sponsored by
University Hospital, Rouen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Metastatic Colorectal Cancer focused on measuring metastatic colorectal cancer, circulating tumor markers, circulating tumor cell, circulating tumor DNA, marker's kinetic

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient has Stage IV colorectal adenocarcinoma histologically proved
  • Patient has at least one measurable lesion
  • Patient has performance status 0-2 on the WHO performance scale
  • Patient is male or female, and > 18 years of age
  • Patient has agree to participate by giving written informed consent

Exclusion Criteria:

  • Patient has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the study.

Sites / Locations

  • Centre François Baclesse
  • University Hospital
  • Centre Frédéric Joliot
  • University Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Tumor markers

Arm Description

measurement of tumor markers ( blood rate of ACE, CA19-9, circulating tumor cell, circulating tumor DNA )

Outcomes

Primary Outcome Measures

Prediction of tumor progression
sensitivity and specificity of CEA kinetic to predict tumor progression at 3 months (RECIST)

Secondary Outcome Measures

Prediction of tumor response
sensitivity and specificity of CEA kinetic to predict tumor response at 3 months (RECIST)

Full Information

First Posted
September 29, 2010
Last Updated
August 16, 2016
Sponsor
University Hospital, Rouen
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1. Study Identification

Unique Protocol Identification Number
NCT01212510
Brief Title
Study of Circulating Markers in Serum of Patients Treated for Metastatic Colorectal Cancer
Acronym
Coca-Colon
Official Title
Study of Circulating Markers in Serum of Patients Treated for Metastatic Colorectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
July 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Rouen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary purpose of the study is to confirm the results of previous study about the usefulness of the serum Carcinoembryonic antigen (CEA) kinetic for chemotherapy monitoring in patients with unresectable metastasis of colorectal cancer (J Clin Oncol 2008;26:3681-6). The secondary purpose is to evaluate the value of circulating free mutant DNA and circulating tumor cells (CTC) and their variations during the treatment.
Detailed Description
Prospective cohort study of patients treated with systemic chemotherapy for unresectable metastatic colorectal cancer. The chemotherapy monitoring is currently based on radiological evaluation (RECIST criteria) and clinical evaluation. Circulating markers as CEA, free mutant DNA, CTC represent an alternative approach. A previous study on usefulness of the serum Carcinoembryonic antigen (CEA) kinetic for chemotherapy monitoring in patients with unresectable metastasis of colorectal cancer has been published (J Clin Oncol 2008;26:3681-6). The present study is designed to validate the previous data. The secondary purpose is to evaluate variations of free mutant DNA and CTC during the chemotherapy. Patients will be included prospectively in 4 centers in Normandy. All systemic chemotherapy and biotherapy validate in this clinical situation by the French National Cancer Institute (INCa) is accepted. Evaluation of response based on RECIST criteria will be performed every 3 months. Blood samples for CEA and CA 19-9 levels will be performed every courses of chemotherapy during first 3 months. Blood samples for detection of free mutant DNA and CTC will be performed at day 1 and 42 of chemotherapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Colorectal Cancer
Keywords
metastatic colorectal cancer, circulating tumor markers, circulating tumor cell, circulating tumor DNA, marker's kinetic

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tumor markers
Arm Type
Other
Arm Description
measurement of tumor markers ( blood rate of ACE, CA19-9, circulating tumor cell, circulating tumor DNA )
Intervention Type
Other
Intervention Name(s)
Blood sampling
Intervention Description
blood rate of ACE, CA19-9, circulating tumor cell, circulating tumor DNA
Primary Outcome Measure Information:
Title
Prediction of tumor progression
Description
sensitivity and specificity of CEA kinetic to predict tumor progression at 3 months (RECIST)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Prediction of tumor response
Description
sensitivity and specificity of CEA kinetic to predict tumor response at 3 months (RECIST)
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient has Stage IV colorectal adenocarcinoma histologically proved Patient has at least one measurable lesion Patient has performance status 0-2 on the WHO performance scale Patient is male or female, and > 18 years of age Patient has agree to participate by giving written informed consent Exclusion Criteria: Patient has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pierre MICHEL, Pr
Organizational Affiliation
UH Rouen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre François Baclesse
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
University Hospital
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
Centre Frédéric Joliot
City
Rouen
ZIP/Postal Code
76000
Country
France
Facility Name
University Hospital
City
Rouen
ZIP/Postal Code
76000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
34112948
Citation
Sefrioui D, Beaussire L, Gillibert A, Blanchard F, Toure E, Bazille C, Perdrix A, Ziegler F, Gangloff A, Hassine M, Elie C, Bignon AL, Parzy A, Gomez P, Thill C, Clatot F, Sabourin JC, Frebourg T, Benichou J, Bouhier-Leporrier K, Gallais MP, Sarafan-Vasseur N, Michel P, Di Fiore F. CEA, CA19-9, circulating DNA and circulating tumour cell kinetics in patients treated for metastatic colorectal cancer (mCRC). Br J Cancer. 2021 Aug;125(5):725-733. doi: 10.1038/s41416-021-01431-9. Epub 2021 Jun 10.
Results Reference
derived

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Study of Circulating Markers in Serum of Patients Treated for Metastatic Colorectal Cancer

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