search
Back to results

Influence of Body Composition on Chemotherapy Outcomes in Localized Breast Cancer (FATTAX)

Primary Purpose

Breast Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
pharmacokinetics blood sample assessment
Sponsored by
Centre Henri Becquerel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Cancer focused on measuring breast cancer, body composition, docetaxel, pharmacokinetics

Eligibility Criteria

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

Inclusion Criteria: Woman older than Early breast cancer CT-scan of less than 3 months, including L3 level Indication of docetaxel at 100 mg/m² as adjuvant CT Exclusion Criteria: HER2 amplified or triple negative tumors Pregnant or breastfeeding women Patients under guardianship or curatorship Concomitant administration of another cytotoxic drug or targeted therapy Psychosocial disorder Administration of another cytotoxic drug or targeted therapy within 20 days prior to blood collection

Sites / Locations

  • Centre Henri Becquerel

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Pharmocokinetics blood sample assessment

Arm Description

during first administration of docetaxel several pharmacokinetics samples will be assessed

Outcomes

Primary Outcome Measures

Comparison of docetaxel area under courb between obese and lean patients

Secondary Outcome Measures

Comparison of docetaxel area under courb between overweight and lean patients
Comparison of docetaxel area under courb according to BMI versus body composition (assessed by CT scan)
Interrelationship of docetaxel area under courb and docetaxel induced side effects
Interrelationship between of body composition and leptine/adiponectine rates

Full Information

First Posted
April 14, 2023
Last Updated
May 11, 2023
Sponsor
Centre Henri Becquerel
Collaborators
Erasmus Medical Center, Universitaire Ziekenhuizen KU Leuven
search

1. Study Identification

Unique Protocol Identification Number
NCT05858398
Brief Title
Influence of Body Composition on Chemotherapy Outcomes in Localized Breast Cancer
Acronym
FATTAX
Official Title
Influence of Body Composition, Total Body Fat and Body Mass Index on the Pharmacokinetics of Docetaxel in Localized Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 30, 2023 (Anticipated)
Primary Completion Date
May 2, 2025 (Anticipated)
Study Completion Date
May 2, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Henri Becquerel
Collaborators
Erasmus Medical Center, Universitaire Ziekenhuizen KU Leuven

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
The purpose of this study is to determine if pharmacokinetics of docetaxel is modified by the body composition (assessed by the BMI but also by CT-scan) in patients treated by docetaxel as adjuvant treatment of a localized breast cancer
Detailed Description
Half of the patients treated for a localized breast cancer are obese or overweighted. Recently published post-hoc analyses of a large randomised trial (BIG-2-98) revealed that BMI could impact the benefit of a docetaxel based chemotherapy, but not of an anthracyclin based chemotherapy. One of the hypothesis is that the distribution volume of hydrophobic drugs, such as docetaxel, may be influenced by the BMI, and more precisely by the amount of total fat. In that context, we aim to assess the docetaxel pharmacokinetics during its first exposure for localized breast cancer, and compare these results according to 3 groups of patients (lean, overweight and obese).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer, body composition, docetaxel, pharmacokinetics

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Pharmocokinetics blood sample assessment
Arm Type
Experimental
Arm Description
during first administration of docetaxel several pharmacokinetics samples will be assessed
Intervention Type
Biological
Intervention Name(s)
pharmacokinetics blood sample assessment
Intervention Description
pharmacokinetics blood sample assessment during the first exposure to docetaxel
Primary Outcome Measure Information:
Title
Comparison of docetaxel area under courb between obese and lean patients
Time Frame
8 hours after the end of first cycle of docetaxel
Secondary Outcome Measure Information:
Title
Comparison of docetaxel area under courb between overweight and lean patients
Time Frame
8 hours after the end of first cycle of docetaxel
Title
Comparison of docetaxel area under courb according to BMI versus body composition (assessed by CT scan)
Time Frame
8 hours after the end of first cycle of docetaxel
Title
Interrelationship of docetaxel area under courb and docetaxel induced side effects
Time Frame
3 months after first cycle of docetaxel
Title
Interrelationship between of body composition and leptine/adiponectine rates
Time Frame
8 hours after the end of first cycle of docetaxel

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Woman older than Early breast cancer CT-scan of less than 3 months, including L3 level Indication of docetaxel at 100 mg/m² as adjuvant CT Exclusion Criteria: HER2 amplified or triple negative tumors Pregnant or breastfeeding women Patients under guardianship or curatorship Concomitant administration of another cytotoxic drug or targeted therapy Psychosocial disorder Administration of another cytotoxic drug or targeted therapy within 20 days prior to blood collection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Florian Clatot, Prof
Phone
+33232082231
Email
florian.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
Florian Clatot, Prof
Organizational Affiliation
Centre Henri Becquerel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Henri Becquerel
City
Rouen
ZIP/Postal Code
76038
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Florian Clatot, Prof
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

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Influence of Body Composition on Chemotherapy Outcomes in Localized Breast Cancer

We'll reach out to this number within 24 hrs