Sunitinib, Cyclophosphamide, and Methotrexate in Treating Patients With Metastatic Breast Cancer

University of California San Francisco (UCSF)

Status and phase

Terminated

Phase 2

Phase 1

Conditions

Breast Cancer

Treatments

Drug: cyclophosphamide

Drug: sunitinib malate

Other: laboratory biomarker analysis

Drug: methotrexate

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00616122

NCI-2011-01275 (Registry Identifier)

057519

Details and patient eligibility

About

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

PURPOSE: This phase I/II trial is studying the side effects and best dose of sunitinib when given together with cyclophosphamide and methotrexate to see how well they work in treating patients with metastatic breast cancer.

Full description

OBJECTIVES:

Primary

To determine the maximum tolerated dose of the combination of metronomic dose cyclophosphamide and methotrexate with continuous dosing sunitinib malate. (Phase I)
To determine the time to disease progression in patients with metastatic breast cancer treated with metronomic dose chemotherapy with cyclophosphamide and methotrexate combined with continuous dosing of sunitinib malate. (Phase II)

Secondary

To determine the response rate in patients receiving this treatment.
To determine the duration of response in patients receiving this treatment.
To determine the toxicity of this regimen in these patients.
To determine the feasibility by assessment of toxicities of this regimen and number of voluntary withdrawals from the study.
To correlate outcome measures with possible surrogate markers including serial measurements of circulating tumor cells and circulating endothelial cells.

OUTLINE: This is a dose-escalation study of sunitinib malate.

Phase I: Patients receive oral sunitinib malate once daily. Beginning 14 days later, patients also receive oral cyclophosphamide once daily on days 1-21 and oral methotrexate twice daily on days 1, 2, 8, 9, 15, and 16. Treatment with sunitinib malate, cyclophosphamide, and methotrexate repeats every 21 days* in the absence of disease progression or unacceptable toxicity.
Phase II: Patients receive sunitinib malate at the maximum tolerated dose determined in phase I and cyclophosphamide and methotrexate as in phase I.

NOTE: *Course 1 includes 2 weeks of sunitinib malate alone followed by sunitinib malate, cyclophosphamide, and methotrexate for 21 days

Blood samples are collected periodically for measurement of circulating tumor cells, circulating endothelial cells, and vascular endothelial growth factor (VEGF) levels.

After completion of study treatment, patients are followed for 30 days and then every 2 months for 1 year.

Enrollment

32 patients

Sex

All

Ages

18 to 120 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

Pathologically confirmed diagnosis of breast cancer with documented progressive disease
- Metastatic disease
Measurable disease as defined by RECIST criteria or evaluable disease
Must have received at least one prior chemotherapy regimen for metastatic breast cancer
- Patients refusing all other chemotherapy for breast cancer may enroll without prior treatment
Patients with HER2-overexpression disease must have been previously treated with trastuzumab (Herceptin®)
Patients with stable brain metastases are eligible
Hormone receptor status not specified

PATIENT CHARACTERISTICS:

Menopausal status not specified
Eastern Cooperative Oncology Group (ECOG) performance status 0-2
Life expectancy ≥ 12 weeks
Absolute Neutrophil Count (ANC) ≥ 1,000/mm³
Platelet count ≥ 100,000/mm³
Creatinine ≤ 1.5 times upper limit of normal (ULN)
aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 times ULN (≤ 5 times ULN in the presence of liver metastases)
Total bilirubin ≤ 1.5 times ULN
Able to take oral medications and maintain hydration
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception during and for 6 months after treatment
No severe concurrent illness including, but not limited to, any of the following:
- Congestive heart failure
- Significant cardiac disease
- Uncontrolled hypertension
Must be able to read and speak English

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
At least 2 weeks since prior treatment, including chemotherapy, hormonal therapy, trastuzumab (Herceptin®), or other targeted therapies
Prior bevacizumab allowed if discontinued for any reason other than toxicity
No potent inducers or inhibitors of CYP3A4 enzymes that effect the metabolism of sunitinib malate
No prior sunitinib malate
No other concurrent investigational therapy
No concurrent radiotherapy
Concurrent bisphosphonates allowed