Pilot Study of Sorafenib and Bi-weekly Capecitabine in Patients With Advanced Breast and Gastrointestinal Tumors

This study is currently recruiting participants.
Verified July 2012 by Yale University
Sponsor:
Collaborator:
Bayer
Information provided by (Responsible Party):
Gina Chung, Yale University
ClinicalTrials.gov Identifier:
NCT01640665
First received: June 5, 2012
Last updated: July 10, 2012
Last verified: July 2012
  Purpose

The purpose of this study is to find the maximum tolerated dose of the combination of two drugs. The two drugs are Sorafenib and Capecitabine. The drug Sorafenib is an approved drug which is used to treat certain cancers. The drug Capecitabine is approved to treat patients with advanced breast cancer as well as early stage colon cancer.


Condition Intervention Phase
Metastatic Breast Cancer
Gastrointestinal Tumors
Drug: Sorafenib, Capecitabine
Phase 1

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Pilot Study of Sorafenib and Bi-weekly Capecitabine in Patients With Advanced Breast and Gastrointestinal Tumors

Resource links provided by NLM:


Further study details as provided by Yale University:

Primary Outcome Measures:
  • Maximum Tolerated Dose / Safety [ Time Frame: 4 weeks ] [ Designated as safety issue: Yes ]

    Primary Objectives:

    • Safety
    • Determination of maximum tolerated dose


Secondary Outcome Measures:
  • Response [ Time Frame: 8 Weeks ] [ Designated as safety issue: No ]

    Secondary Objectives:

    • Overall Response Rate
    • Duration of Response


Estimated Enrollment: 15
Study Start Date: July 2012
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: Sorafenib, Capecitabine
    One cycle will consist of 4 weeks of treatment. The dose of Sorafenib will be 600 mg administered orally daily in divided doses. Capecitabine will be given at a fixed dose of 2000 mg orally BID x 7 days every 14 days.
    Other Name: Sorafenib (Nexavar), Capecitabine (Xeloda)
Detailed Description:

This is a pilot study of Sorafenib combined with Capecitabine in patients with histologically confirmed unresectable or metastatic breast and GI tumors. One cycle will consist of 4 weeks of treatment. The dose of Sorafenib will be 600 mg administered orally daily in divided doses. Capecitabine will be given at a fixed dose of 2000 mg orally BID x 7 days every 14 days

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age ≥ 18 years.
  • Life expectancy of at least 12 weeks (3 months).
  • ECOG Performance Status 0 or 1.
  • Histologically confirmed unresectable or metastatic breast and/or GI tumors for which curative standard treatments are unavailable
  • Adequate bone marrow, liver and renal function as assessed by the following:

    • Hemoglobin > 9.0 g/dl
    • Absolute neutrophil count (ANC) >1,500/mm3
    • Platelet count > 100,000/mm3
    • Total bilirubin < 1.5 times ULN
    • ALT and AST < 2.5 times the ULN ( < 5 x ULN for patients with liver involvement)
    • GFR > 30 ml/min
  • All acute toxic effects (excluding alopecia and neuropathy) of any prior treatment have resolved to NCI-CTCAE v4.0 Grade 1 or less at the time of signing the Informed Consent Form (ICF).
  • Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of study drug. Post-menopausal women (defined as no menses for at least 1 year) and surgically sterilized women are not required to undergo a pregnancy test.
  • Subjects (men and women) of childbearing potential must agree to use adequate contraception beginning at the signing of the ICF until at least 30 days after the last dose of study drug. The definition of adequate contraception will be based on the judgment of the principal investigator or a designated associate.
  • Subject must be able to swallow and retain oral medication.
  • Subjects must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.

Exclusion Criteria:

  • Metastatic brain or meningeal tumors (unless subject completed definitive therapy more than 1 month previously and is stable off steroids).
  • Uncontrolled hypertension defined as systolic blood pressure > 140 mmHg or diastolic pressure > 90 mmHg, despite optimal medical management.
  • Active or clinically significant cardiac disease including:

    • Congestive heart failure - New York Heart Association (NYHA) > Class II.
    • Active coronary artery disease.
    • Cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers or digoxin.
    • Unstable angina (anginal symptoms at rest), new-onset angina within 3 months before randomization, or myocardial infarction within 6 months before randomization.
  • Subject with any pulmonary hemorrhage/bleeding event of NCI-CTCAE v4.0 Grade 2 or higher within 4 weeks of study enrollment; any other hemorrhage/bleeding event of NCI-CTCAE v4.0 Grade 3 or higher within 4 weeks of study enrollment.
  • Major surgery, open biopsy or significant traumatic injury within 30 days of first study drug.
  • Presence of an active non-healing wound, non-healing ulcer, or bone fracture.
  • Thrombotic or embolic events such as a cerebrovascular accident (including transient ischemic attacks) within 3 month of informed consent.
  • Anticoagulation with warfarin is not permitted.
  • Evidence or history of bleeding diathesis or coagulopathy.
  • Subjects who have used strong CYP3A4 inducers (eg, phenytoin, carbamazepine, phenobarbital, St. John's Wort [Hypericum perforatum], dexamethasone at a dose of greater than 16 mg daily, or rifampin [rifampicin], and/or rifabutin) within 30 days of trial enrollment.
  • Subjects with a history of dihydopyrimidine dehydrogenase (DHPD) deficiency or severe and unexpected reactions to fluropyrimidines.
  • Subjects with any previously untreated or concurrent cancer that is distinct in primary site or histology except cervical cancer in-situ, treated basal cell carcinoma, or superficial bladder tumor. Subjects surviving a cancer that was curatively treated and without evidence of disease for more than 3 years before randomization are allowed. All relevant cancer treatments must be completed at least 3 years prior to study entry (i.e., signature date of the informed consent form).
  • History of organ allograft. (Including corneal transplant).
  • Known human immunodeficiency virus (HIV) infection or Hepatitis B or C currently undergoing active antiviral treatment.
  • Any malabsorption problem.
  • Anticancer chemotherapy or immunotherapy during the study is not permitted.
  • Known or suspected allergy or hypersensitivity to any of the study drugs, study drug classes, or excipients of the formulations given during the course of this trial.
  • Women who are pregnant or breast-feeding.
  • Inability to comply with the protocol and/or not willing or not available for follow-up assessments.
  • Any condition which, in the investigator's opinion, makes the subject unsuitable for trial participation.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01640665

Contacts
Contact: Yale Cancer Center 203-785-5702

Locations
United States, Connecticut
Yale Cancer Center Recruiting
New Haven, Connecticut, United States, 06519
Contact: Yale Cancer Center    203-785-5702      
Principal Investigator: Gina Chung, MD         
Sponsors and Collaborators
Yale University
Bayer
Investigators
Principal Investigator: Gina Chung, MD Yale University
  More Information

Additional Information:
No publications provided

Responsible Party: Gina Chung, Assistant Professor of Medical Oncology, Yale University
ClinicalTrials.gov Identifier: NCT01640665     History of Changes
Other Study ID Numbers: GC0212
Study First Received: June 5, 2012
Last Updated: July 10, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by Yale University:
histologically
unresectable
metastatic
Phase 1
Breast Cancer
GI Tumors
Sorafenib
Capecitabine

Additional relevant MeSH terms:
Breast Neoplasms
Digestive System Neoplasms
Gastrointestinal Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases
Digestive System Diseases
Gastrointestinal Diseases
Capecitabine
Fluorouracil
Sorafenib
Antimetabolites, Antineoplastic
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Antineoplastic Agents
Therapeutic Uses
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Protein Kinase Inhibitors
Enzyme Inhibitors

ClinicalTrials.gov processed this record on April 15, 2014