Gemcitabine +/- Imatinib Mesylate, Patients w/Previously Treated Metastatic Breast Cancer

Rutgers The State University of New Jersey

Status and phase

Terminated

Phase 2

Conditions

Breast Cancer

Treatments

Drug: gemcitabine hydrochloride

Drug: imatinib mesylate

Study type

Interventional

Funder types

Other

Industry

NIH

Identifiers

NCT00323063

P30CA072720 (U.S. NIH Grant/Contract)

NJ1105 (Other Identifier)

CDR0000539445 (Other Identifier)

0220060081 (Other Identifier)

NCI-2012-00520 (Other Identifier)

040504

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Imatinib mesylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving gemcitabine together with imatinib mesylate may kill more tumor cells.

PURPOSE: This randomized phase II trial is studying gemcitabine and imatinib mesylate to see how well they work compared to gemcitabine alone in treating patients with previously treated locally advanced or metastatic breast cancer.

Full description

OBJECTIVES:

Primary

Compare time to progression in patients with previously treated locally advanced or metastatic breast cancer treated with gemcitabine hydrochloride with vs without imatinib mesylate.

Secondary

Compare the efficacy of these regimens in these patients.
Compare the overall survival of patients treated with these regimens.
Compare the safety and tolerability of these regimens in these patients.

OUTLINE: This is a multicenter, open-label, randomized study. Patients are randomized to 1 of 2 treatment arms.

Arm I: Patients receive gemcitabine hydrochloride IV on days 3 and 10.
Arm II: Patients receive gemcitabine hydrochloride IV on days 3 and 10 and oral imatinib mesylate once daily on days 1-5 and 8-12.

In both arms, treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 80 patients will be accrued for this study.

Enrollment

49 patients

Sex

All

Ages

18 to 120 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

Histologically confirmed breast cancer
- Locally advanced or metastatic disease
- Disease progression after at least 1 prior chemotherapy regimen for metastatic disease
  - No more than 2 prior chemotherapy regimens for metastatic disease (prior neoadjuvant or adjuvant treatment will not be included in determining the number of prior chemotherapy regimens)
Measurable disease
No known symptomatic or untreated brain metastases or carcinomatous meningitis
- Previously treated and clinically stable brain metastases allowed provided patient has been off steroids for > 7 days
Hormone receptor status not specified

PATIENT CHARACTERISTICS:

Male or female
Menopausal status not specified
ECOG performance status 0-2
Life expectancy ≥ 3 months
Absolute neutrophil count ≥ 1,500/mm^3
Platelet count ≥ 100,000/mm^3
Bilirubin ≤ 1.5 times upper limit of normal (ULN)
AST or ALT ≤ 2.5 times ULN
Creatinine ≤ 1.5 times ULN OR creatinine clearance ≥ 60 mL/min
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception during and for 3 months after completion of study therapy
Able to swallow oral medication
No coexisting medical condition that would preclude study compliance
No uncontrolled illness, including any of the following:
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Cardiac arrhythmia requiring therapy
- Myocardial infarction within the past 6 months
- Active infection
No New York Heart Association class III-IV cardiac disease
No history of allergic reaction attributed to compounds of similar chemical or biologic composition to gemcitabine hydrochloride and/or imatinib mesylate
No other primary malignancies within the past 5 years except for carcinoma in situ of the cervix or nonmelanoma skin cancer
No known chronic liver disease (i.e., chronic active hepatitis or cirrhosis)
No known HIV infection

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
Recovered from all prior therapy
More than 2 weeks since prior surgery
At least 2 weeks since prior hormonal therapy
At least 2 weeks since prior trastuzumab (Herceptin®)
At least 3 weeks since prior chemotherapy (6 weeks for nitrosoureas)
At least 3 weeks since prior anti-vascular endothelial growth factor therapy
More than 28 days since prior investigational agents
At least 3 weeks since prior radiotherapy
- Must have evidence of ≥ 1 measurable target lesion outside the irradiated fields OR radiologically confirmed disease progression within the irradiated fields after completion of radiotherapy
No prior imatinib mesylate for metastatic disease
No prior gemcitabine hydrochloride for metastatic disease
More than 6 months since prior adjuvant gemcitabine hydrochloride
No other concurrent investigational or commercial agents
No concurrent therapeutic anticoagulation with warfarin (e.g., Coumadin® or Coumadine®)
- Concurrent heparin or low-molecular weight heparin (e.g., Lovenox®) for therapeutic anticoagulation allowed
- Concurrent prophylactic warfarin therapy (e.g., mini-dose Coumadin® ≤ 1 mg daily) to maintain catheter patency allowed
No concurrent routine chronic systemic corticosteroids
No concurrent medications that would preclude study compliance