A Study to Compare Vincristine to Sirolimus for Treatment of High Risk Vascular Tumors

Status: Recruiting
Phase: Phase 2
DFCI Protocol ID:

In this research study we want to learn more about which treatment works better for patients diagnosed with a vascular tumor called Kaposiform Hemangioendothelioma (KHE) or other high risk vascular tumors such as Tufted Angioma (TA). In these tumors, the blood cells that help your blood clot called platelets become trapped in the tumor causing swelling, pain, and bruising. Vascular tumors can be life threatening. There are few medical treatments that will work to shrink the vascular tumor. Some doctors will use steroids and vincristine to try and shrink vascular tumors. In this research study, the study doctor will compare two different drugs to see which one will work better to help shrink your vascular tumor. One of the drugs is vincristine. Vincristine is approved by the Food and Drug Administration (FDA) to treat people with cancer. Vincristine is used to stop the abnormal cells from growing such as cells that make up blood vessels. The other drug to be used in this study is sirolimus. Sirolimus is currently approved by the Food and Drug Administration (FDA) to prevent transplanted organ rejection. Sirolimus is not approved by the FDA for treatment of vascular abnormalities and is considered experimental. Sirolimus belongs to a class of drugs call 'mTOR inhibitors'. mTOR (mammilian target of rapamycin) helps cells to grow and may also help blood vessels to grow in a more normal fashion. Sirolimus is currently being tested in patients with vascular tumors and cancer. In vascular tumors, we hope sirolimus will stop the blood vessel growth. Funding Source: FDA - OOPD (Office of Orphan Products Development)

Conducting Institutions:

Children's Hospital Boston, Dana-Farber Cancer Institute

Overall PI:

Cameron Trenor, MD, Children's Hospital Boston

Site-responsible Investigators:

Contacts:

Dana-Farber Cancer Institute: Childrens Hospital Pediatric Clinical Translation Investigation Program CTIP, ctip@partners.org

Eligibility Criteria

Inclusion Criteria:

  -  Diagnosis: All patients must have one of the following vascular anomalies as
     determined by clinical, radiologic and histologic criteria (when possible). Biopsy
     strongly recommended (but not required) with suggested immunostains: CD34, PROX-1 or
     D240, Glut-1 and MIB-1.

       1. Kaposiform Hemangioendotheliomas

       2. Tufted angioma

High Risk Stratification: In addition to the above diagnosis, all of the following
criteria need to be met:

a. Kasabach Merritt Syndrome defined at a platelet counts less than 50,000 K/µl and/or
fibrinogen level < 100 mg/dl at the time of diagnosis.

  -  Age: Patients must be 0 - 31 years of age at the time of study entry. Enrollment
     includes patients of both genders and all ethnic groups.

  -  Organ function requirements:

       1. Adequate liver function defined as:

    1. Total bilirubin ≤ 1.5 x ULN for age, and

    2. SGPT (ALT) ≤ 5 x ULN for age, and

    3. Serum albumin >/= 2 g/dL.

    4. Fasting LDL cholesterol of <160 mg/dL

    5. Fasting triglyceride <400 mg/dl

       2. Adequate Bone Marrow Function defined as:

    1. Peripheral absolute neutrophil count (ANC) >/= 1000/uL

    2. Hemoglobin >/= 8.0 g/dL (may receive RBC transfusions)

    3. No Platelet requirement

       3. Adequate Renal Function Defined as:

    1. A serum creatinine based on age as follows:

       Age (Years) Maximum Serum Creatinine (mg/dL)

 -  5 0.8 6 to ≤10 1.0 11 to ≤15 1.2 >15 1.5

    2. Urine protein to creatinine ratio (UPC) < 0.3 g/l

  -  Performance Status: Karnofsky >/= 50 (≥16 years of age) and Lansky >/= 50 for
     patients <16 years of age.

  -  Prior therapy

       1. Patients who have undergone surgical resection or interventional radiology
  procedures for disease control are eligible if they meet all inclusion criteria
  after surgery/procedure

       2. Surgery: At least 2 weeks since undergoing any major surgery

       3. Radiation: > 6 months from involved field radiation

       4. Prior vincristine therapy is permitted. Patients may also have received up to 2
  doses of vincristine prior to randomization.

Exclusion Criteria:

  -  Concurrent severe and/or uncontrolled medical disease that could compromise
     participation in the study (e.g. uncontrolled diabetes, uncontrolled hypertension,
     severe infection, severe malnutrition, chronic liver or renal disease, active upper
     GI tract ulceration).

  -  Patients who require medications that are strong inhibitors/inducers CYP3A4 enzyme
     activity, including anticonvulsants, (Appendix II) to control concurrent medical
     conditions are not eligible. Patients who discontinue use of prohibited medications
     with a one week washout prior to start of study treatment are eligible.

  -  Known history of HIV seropositivity or known immunodeficiency. Testing is not
     required unless a condition is suspected.

  -  Impairment of gastrointestinal function or gastrointestinal disease that may
     significantly alter the absorption of sirolimus (e.g. ulcerative disease,
     uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel
     resection). A gastric tube or nasogastric tube is allowed.

  -  Females who are pregnant or breast feeding.

  -  Males or females of reproductive potential may not participate unless they have
     agreed to use an effective contraceptive method during the period they are receiving
     the study drug and for 3 months thereafter. Abstinence is an acceptable method of
     birth control. Females of childbearing potential will be given a pregnancy test
     within 7 days prior to administration of study treatment and must have a negative
     urine or serum pregnancy test.

  -  Patients who have received prior treatment with an mTOR inhibitor.

  -  Patients unwilling or unable to comply with the protocol or who in the opinion of the
     investigator may not be able to comply with the safety monitoring requirements of the
     study.

  -  Patients who currently have an uncontrolled infection, defined as receiving
     intravenous antibiotics.

Know Your Options

Not sure which clinical trials might be right for your child? Email our clinical trials team at clinicaltrials@danafarberbostonchildrens.org.
We can help you navigate your options.

Get Clinical Trial Updates

 

Stay informed about Dana-Farber/Boston Children's research efforts, including information on new and current clinical trials. Sign up to receive our email newsletter Advances in Pediatric Hematology/Oncology.

Download Our Clinical Trials

Download a list of our open clinical trials. Check back regularly for updates.