Trial Search Results

Phase I Oral mTOR Inhibitor RAD001 in Combo w/ Capecitabine for Metastatic Breast

In order to improve the survival of metastatic breast patients, it is important to investigate the use of novel therapeutic agents combined with known active agents in the treatment of breast cancer. This is a phase I study evaluating the maximum tolerated doses and toxicities of RAD001 in combination with capecitabine for the treatment of metastatic breast cancer. RAD001 (INN: everolimus) is a novel macrolide, which is being developed as an antiproliferative drug with applications as an immunosuppressant and anticancer agent. Phase I trials in patients with solid tumors have shown that treatment with RAD001 is well-tolerated with a minimal side effect profile. Capecitabine (Xeloda, Roche) is an oral fluoropyrimidine that was approved in 1998 for the treatment of patients with metastatic breast cancer. The all-oral regimen of RAD001 with capecitabine is an attractive approach as the treatment of metastatic breast cancer has not yet proven to be curative. We also want to find out what possible benefit this combination of drugs might have on treating your cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Stanford University

Collaborator: Novartis

Stanford Investigator(s):

Intervention(s):

  • Drug: Capecitabine
  • Drug: RAD001

Phase:

Phase 1

Eligibility


Inclusion Criteria:Patients meeting all of the following criteria are eligible for this
trial:

   1. Histologically-confirmed metastatic breast cancer.

   2. Measurable disease either by clinical exam or radiographs.

   3. Patients must be fully recovered from acute toxicity of prior therapy.

   4. Patients must not have received prior therapy with capecitabine.

   5. Patients must not have received more than 3 prior chemotherapy regimens for metastatic
   breast cancer.

   6. Patients must not be receiving concurrent endocrine therapy or immunotherapy.

   7. Patients must have an expected survival of at least 3 months.

   8. Patients should have ECOG performance status 0 or 1 (KPS 100-80%).

   9. Patients should have adequate bone marrow, hepatic and renal function.

      - WBC >= 3000/mm^3,

      - ANC > 1500,

      - Hgb > 9 g/dL,

      - Platelets >= 100,000/mm^3,

      - total bilirubin<1 .5 mg/dL,

      - AST/ALT<2.5 x normal {<= 5x ULN in patients with liver metastases}

      - creatinine<2 mg/dL);

10. Fasting serum cholesterol ˜300 mg/dL OR ˜7.75 mmol/L AND fasting triglycerides ˜2.5 x
   ULN. (Note: In case one or both of these thresholds are exceeded, the patient can only
   be included after initiation of appropriate lipid lowering medication.)

11. Patients must be >18 years of age

12. Signed informed consent

Exclusion Criteria:Patients meeting any of the following criteria will not be eligible for
the trial:

   1. Patients who have received other chemotherapy or endocrine therapy and not recovered
   from acute toxicity of previous therapy.

   2. Patients who have received radiotherapy within 4 weeks prior to start of this trial.

   3. Patients who have undergone major surgery within 2 weeks of study enrollment.

   4. Patients with known evidence of brain metastases or leptomeningeal disease, ,
   including patients who continue to require glucocorticoids for brain or leptomeningeal
   metastases..

   5. Patients with a history of other cancers except curatively-treated carcinoma of the
   cervix in situ or non-melanomatous skin cancer. Patients with other cancers thought to
   be cured may be entered into the trial after discussion with and approval of the study
   chair.

   6. Patients with an active serious infection or other serious underlying medical
   condition that would impair their ability to receive protocol treatment.

   7. Patients with bone metastases as their only site of measurable disease.

   8. Dementia or significantly altered mental status that would prohibit the understanding
   and/or giving of informed consent.

   9. Pregnant or breast-feeding patients.

10. Patients not using adequate methods of birth control if still of child-bearing
   potential.

11. Patients who have received prior therapy with capecitabine.

12. Patients who have received more than 3 prior chemotherapy regimens for metastatic
   breast cancer.

13. Patients receiving other investigational therapy.

14. Patients who have received prior treatment with experimental therapy within 30 days
   prior to start of trial.

15. Patients who receive chronic systemic steroids or other immunosuppressive agents.

16. Patients with a known history of HIV.

17. Patients with impaired gastrointestinal function which may significantly decrease
   absorption of RAD001 and capecitabine.

18. Patients with an active, bleeding diathesis or receiving anti-vitamin K therapy.
   (except low dose coumadin)

19. Patients who have had prior treatment with an mTOR inhibitor (sirolimus, temsirolimus,
   everolimus).

20. Patients who have any sever and/or uncontrolled medical conditions or other conditions
   that could affect their participation in the study such as:

      - with uncontrolled diabetes mellitus,

      - uncontrolled hypertension,

      - severe malnutrition,

      - unstable angina, or congestive heart failure - New York Heart Association Class
      III or IV, ventricular arrhythmias, active ischemic heart disease,

      - myocardial infarction within 6 months, chronic liver disease such as cirrhosis,
      chronic active hepatitis or chronic persistent hepatitis /

         - renal disease,

         - Impairment of gastrointestinal function or gastrointestinal disease that may
         significantly alter the absorption of RAD001 (e.g., ulcerative disease,
         uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small
         bowel resection)

21. Patients who have had prior bone marrow or stem cell transplant.

22. Patients receiving tube feeding or TPN, or who are 75% or less of their ideal body
   weight.

23. Patients with a caloric intake of less than 500 calories per day.

24. History of noncompliance to medical regimens

25. Patients unwilling to or unable to comply with the protocol

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Female

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Mary Chen
6507238686