Ixabepilone and SBRT For Metastatic Breast Cancer

METASTATIC BREAST CANCER Clinical Trial

Official title:

A Phase II Trial Of Ixabepilone and Stereotactic Body Radiation Therapy (SBRT) For Patients With Triple Negative Metastatic Breast Cancer

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01818999
• Other study ID #: STU 102012-020
• Status: Withdrawn
• Phase: Phase 2
• Start date: August 2013
• Est. completion date: April 2015

Study information

• Verified date: January 2019
• Source: University of Texas Southwestern Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is being done to find the effect of Stereotactic body radiation therapy (SBRT) in combination with Ixabepilone for women with triple negative metastatic breast cancer.

Description:

Ixabepilone is a FDA approved drug for the treatment of metastatic or locally advanced breast cancer after failure of chemotherapy. SBRT is a treatment method to deliver a high dose of radiation to the target, utilizing either a single dose or a small number of treatments with a high degree of precision within the body. The combination of Ixabepilone with SBRT is not an approved treatment at this time.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: April 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 99 Years

Eligibility

Inclusion Criteria:

1. Biopsy proven triple negative invasive ductal or lobular metastatic breast cancer. Tumor estrogen, progesterone, and HER2 (tested by IHC or FISH) negative disease. (ER- defined as </=1% by IHC, PR- defined as </=1% by IHC, and HER2- by IHC 1+. If HER2 result by IHC is 2+ (equivocal), the tumor must be confirmed to be HER2- by FISH.

2. Age = 18 years.

3. Patients must not have started Ixabepilone treatment more than 5 weeks prior to initiation of SBRT treatment.

4. Patients can have up to 6 sites of active extracranial disease(</=3 in the liver = one site and </=3 in the lung= one site) identified by CT scan, or PET/CT, within 8 weeks prior to initiation of SBRT (up to 2 contiguous vertebral metastasis will be considered a single site of disease). Maximum number of lesions treated is deemed as feasible per the treating radiation oncologist; ie: A patient with 4 right axillary lymph nodes, L1-L2 bone metastasis, 3 lung lesions, 1 left lung lesion, 2 liver lesions, and T2-T3 bone metastasis would be defined as having 6 sites of disease. Criteria to define a lesion in any location as a metastasis requiring local treatment as one of the sites for SBRT is any lesion clinically felt to be viable; defined as enlarging on CT/MRI or having persistent FDG avidity (Either SUV>3 or increase of SUV>20% over a 6 month interval).

5. Patients with skin nodules, skin invasion, or skin ulceration are eligible, if treatment with conventional radiation (at discretion of radiation oncologist) or surgery is planned. SBRT to skin nodules is not advised because of risk of skin necrosis.

6. . Patients must have had failure of an anthracycline, a taxane and capecitabine as per FDA approved criteria.

7. Performance status of ECOG 0,1, or 2.

8. Adequate organ and marrow function as defined below:

• leukocytes = 3,000/mcL

• absolute neutrophil count = 1,500/mcL

• platelets = 100,000/mcl

• total bilirubin within normal institutional limits

• AST(SGOT)/ALT(SPGT) = 2.5 X institutional upper limit of normal

• creatinine within normal institutional limits

9. Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

9.1 A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:

• Has not undergone a hysterectomy or bilateral oophorectomy; or

• Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months).

10. Patients who would be receiving SBRT for lung tumors who are known or must have a documented forced expiratory volume in 1 second (FEV1)>/=30%.

11. Must have a CT C/A/P, or PET/CT scan within 8 weeks of enrollment.

12. Ability to understand and the willingness to sign a written informed consent

Exclusion Criteria:

1. Patients may not be actively receiving any other investigational agents.

2. Patients with untreated brain metastasis (patients can have whole brain radiation or stereotactic radiation to brain prior to enrollment).

3. Patients with leptomeningeal disease.

4. History of allergic reactions attributed to compounds of similar chemical or biologic composition to Agent(s) used in study. Patients with a history of severe reactions to Cremephor EL or its derivatives (polyoxyethylated castor oil) are ineligible as Ixabepilone contraindicated in these patients

5. Because the tolerance dose of SBRT to the gastrointestinal tract is not established, patients with metastatic disease invading the esophagus, stomach, intestines, or mesenteric lymph nodes will not be eligible.

6. Patients with more than 6 discrete extra-cranial sites.

7. Treatment for other carcinomas within the last 5 years, except cured non-melanoma skin and treated in-situ cancers.

8. Patients must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.

9. Patients must not be on concomitant CYP3A4 inhibitors or inducers (see section 4.3).

Related Conditions & MeSH terms

• Breast Neoplasms
• METASTATIC BREAST CANCER

Intervention

Drug:
• IXABEPILONE
injection

Radiation:
• STEREOTACTIC BODY RADIATION THERAPY
SBRT will begin between 1 and 5 weeks after the initiation of Ixabepilone. Patients will receive one, three, or five fractions.

Locations

Country	Name	City	State
United States	University of Texas Southwestern	Dallas	Texas

Sponsors (1)

Lead Sponsor	Collaborator
University of Texas Southwestern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The effect of SBRT in combination with Ixabepilone on median progression free survival	To evaluate the effect of SBRT in combination with Ixabepilone on median progression free survival. Progression free survival is defined as time from initiation of treatment to progressive disease or death	5 years
Secondary	In-field local control and out-of field disease progression rates	To describe the in-field local control and out-of field disease progression rates	5 years
Secondary	Safety of SBRT in combination with Ixabepilone for patients with metastatic triple negative breast cancer after prior chemotherapy	Evaluate the safety of SBRT in combination with Ixabepilone for patients with metastatic triple negative breast cancer after prior chemotherapy	1 year
Secondary	The duration of Ixabepilone usage and time to initiation of next line systemic agent (chemotherapy or biologic agent)	Evaluate the duration of Ixabepilone usage and time to initiation of next line systemic agent (chemotherapy or biologic agent)	5 year
Secondary	Overall survival for patients with metastatic triple negative breast treated with SBRT in combination with Ixabepilone	Evaluate overall survival for patients with metastatic triple negative breast treated with SBRT in combination with Ixabepilone	5 year
Secondary	Generation of an immune response to tumor cells	Evaluate generation of an immune response to tumor cells	1 year