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Study Assessing Efficacy of ZARNESTRA™ Combined With Tamoxifen in Patients With Advanced or Metastatic Breast Cancer

Primary Purpose

Breast Neoplasms

Status
Terminated
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Tamoxifen
Zarnestra
Sponsored by
Institut Claudius Regaud
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Neoplasms focused on measuring Breast Neoplasms, Zarnestra, Tamoxifen, estrogen receptor, progesterone receptor

Eligibility Criteria

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

Inclusion Criteria: Histologically proven, metastatic or locally advanced inoperable breast cancer Tumor considered potentially hormone-sensitive, i.e. presence by IHC of hormone receptors for estrogens (ER+ for more than 10% of cells) and/or progesterone (Pg+ for more than 10% of cells) or both. This expression may have been detected on the primary tumor or at a metastatic site. The method used will be reassessed by IHC if it involves a radioligand technique whenever it is possible to obtain histological material. Progressing on treatment with tamoxifen, given either as adjuvant treatment or for advanced/metastatic breast cancer. Any previous treatment with a steroidal or nonsteroidal antiaromatase in a neo-adjuvant, adjuvant or metastatic situation is permitted. Likewise, any previous treatment with chemotherapy and/or herceptin in a nonmetastatic situation is permitted. Post-menopausal patients Age > 18 years At least one measurable lesion according to the Response Evaluation Criteria for Solid Tumors (RECIST) criteria; for patients who only have bone metastases, an evaluable non-irradiated lytic lesion is required Performance Status (WHO): PS ≤ 2 (Appendix 1). Laboratory tests in accordance with the following criteria: Neutrophils ≥ 2x109/l,Platelets ≥ 100x109/l,Hemoglobin ≥ 10 g/dl, ASAT, ALAT ≤ 2.5 N , or < 5 N when liver metastasis,bilirubin ≤ 1.5 N creatinin ≤ 1.5 N Signed, written consent before any study-related procedure Exclusion Criteria: Men Pre-menopausal patients who are not receiving concurrent LHRH agonist therapy ER- and PR-negative patients Contraindication to antiestrogens (thromboembolic risk) or ZARNESTRA Non metastatic tumor susceptible to management by radiotherapeutic and/or surgical means T4d inflammatory tumor (PEV 2 or 3). Short-term, life-threatening lesions: hepatic invasion > 1/3 of liver volume, pulmonary lymphangitis, uncontrolled cerebral metastases, carcinomatous meningitis Sensory neuropathy > or = grade 1 (WHO) Previous history of uncontrolled cancers or controlled for less than 5 years, except basal cell skin cancers and in situ cancers of the cervix. Chronic diseases (somatic or psychiatric) with a poor prognosis subjects with enzyme-inducing anti-convulsants (e.g., phenytoin, phenobarbital, carbamazepine) : this treatment is not permitted while taking ZARNESTRA Patients who, for family, social, geographic or psychological reasons, could not be followed up correctly.

Sites / Locations

  • Institut Bergonie
  • Institut Val d'Aurelle_ Paul Lamarque
  • Institut Claudius Regaud

Outcomes

Primary Outcome Measures

To evaluate the objective response rate when ZARNESTRA is added to administration of tamoxifen in patients suffering from metastatic or advanced inoperable breast cancer, who are progressing on tamoxifen treatment

Secondary Outcome Measures

To evaluate the time to progression
To evaluate the clinical benefit (response + stable disease at 6 months)
To evaluate the safety of the combination ZARNESTRA and tamoxifen
To evaluate a possible pharmacokinetic interaction between ZARNESTRA and tamoxifen
To evaluate the biological predictive and prognostic factors of a response

Full Information

First Posted
September 13, 2005
Last Updated
November 10, 2006
Sponsor
Institut Claudius Regaud
Collaborators
Janssen-Cilag Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT00210028
Brief Title
Study Assessing Efficacy of ZARNESTRA™ Combined With Tamoxifen in Patients With Advanced or Metastatic Breast Cancer
Official Title
Open, Single-Arm Phase II Study Assessing Efficacy of ZARNESTRA™ Combined With Tamoxifen in Patients With Advanced or Metastatic Breast Cancer Expressing the Estrogen and/or Progesterone Receptor
Study Type
Interventional

2. Study Status

Record Verification Date
November 2006
Overall Recruitment Status
Terminated
Study Start Date
August 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2008 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Institut Claudius Regaud
Collaborators
Janssen-Cilag Ltd.

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate the objective response rate when ZARNESTRA is added to treatment with tamoxifen

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasms
Keywords
Breast Neoplasms, Zarnestra, Tamoxifen, estrogen receptor, progesterone receptor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Tamoxifen
Intervention Type
Drug
Intervention Name(s)
Zarnestra
Primary Outcome Measure Information:
Title
To evaluate the objective response rate when ZARNESTRA is added to administration of tamoxifen in patients suffering from metastatic or advanced inoperable breast cancer, who are progressing on tamoxifen treatment
Secondary Outcome Measure Information:
Title
To evaluate the time to progression
Title
To evaluate the clinical benefit (response + stable disease at 6 months)
Title
To evaluate the safety of the combination ZARNESTRA and tamoxifen
Title
To evaluate a possible pharmacokinetic interaction between ZARNESTRA and tamoxifen
Title
To evaluate the biological predictive and prognostic factors of a response

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven, metastatic or locally advanced inoperable breast cancer Tumor considered potentially hormone-sensitive, i.e. presence by IHC of hormone receptors for estrogens (ER+ for more than 10% of cells) and/or progesterone (Pg+ for more than 10% of cells) or both. This expression may have been detected on the primary tumor or at a metastatic site. The method used will be reassessed by IHC if it involves a radioligand technique whenever it is possible to obtain histological material. Progressing on treatment with tamoxifen, given either as adjuvant treatment or for advanced/metastatic breast cancer. Any previous treatment with a steroidal or nonsteroidal antiaromatase in a neo-adjuvant, adjuvant or metastatic situation is permitted. Likewise, any previous treatment with chemotherapy and/or herceptin in a nonmetastatic situation is permitted. Post-menopausal patients Age > 18 years At least one measurable lesion according to the Response Evaluation Criteria for Solid Tumors (RECIST) criteria; for patients who only have bone metastases, an evaluable non-irradiated lytic lesion is required Performance Status (WHO): PS ≤ 2 (Appendix 1). Laboratory tests in accordance with the following criteria: Neutrophils ≥ 2x109/l,Platelets ≥ 100x109/l,Hemoglobin ≥ 10 g/dl, ASAT, ALAT ≤ 2.5 N , or < 5 N when liver metastasis,bilirubin ≤ 1.5 N creatinin ≤ 1.5 N Signed, written consent before any study-related procedure Exclusion Criteria: Men Pre-menopausal patients who are not receiving concurrent LHRH agonist therapy ER- and PR-negative patients Contraindication to antiestrogens (thromboembolic risk) or ZARNESTRA Non metastatic tumor susceptible to management by radiotherapeutic and/or surgical means T4d inflammatory tumor (PEV 2 or 3). Short-term, life-threatening lesions: hepatic invasion > 1/3 of liver volume, pulmonary lymphangitis, uncontrolled cerebral metastases, carcinomatous meningitis Sensory neuropathy > or = grade 1 (WHO) Previous history of uncontrolled cancers or controlled for less than 5 years, except basal cell skin cancers and in situ cancers of the cervix. Chronic diseases (somatic or psychiatric) with a poor prognosis subjects with enzyme-inducing anti-convulsants (e.g., phenytoin, phenobarbital, carbamazepine) : this treatment is not permitted while taking ZARNESTRA Patients who, for family, social, geographic or psychological reasons, could not be followed up correctly.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henri Roché, Pr
Organizational Affiliation
Institut Claudius Regaud
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Bergonie
City
Bordeaux
Country
France
Facility Name
Institut Val d'Aurelle_ Paul Lamarque
City
Montpellier
Country
France
Facility Name
Institut Claudius Regaud
City
Toulouse
Country
France

12. IPD Sharing Statement

Learn more about this trial

Study Assessing Efficacy of ZARNESTRA™ Combined With Tamoxifen in Patients With Advanced or Metastatic Breast Cancer

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