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

This study is currently recruiting participants.
Verified July 2017 by Denise Martin Adams, Boston Children's Hospital
Sponsor:
ClinicalTrials.gov Identifier:
NCT02110069
First Posted: April 10, 2014
Last Update Posted: July 13, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborator:
Pfizer
Information provided by (Responsible Party):
Denise Martin Adams, Boston Children's Hospital
April 8, 2014
April 10, 2014
July 13, 2017
June 14, 2017
June 2021   (Final data collection date for primary outcome measure)
  • Change in hematologic parameters [ Time Frame: 2 months ]
    Hematologic parameters are defined as a platelet count greater than 50,000/uL (or a 2 times increase in platelet count compared to baseline) and a fibrinogen level greater than 100mg/dl.
  • Number of Serious and Non-Serious Adverse Events [ Time Frame: 2 months; 12 months ]
    Serious and non-serious adverse events will be recorded for all participants and graded using CTCAE v4.0 (Common Toxicity Criteria for Adverse Effects). Adverse event rates will be calculated for both sirolimus and vincristine.
Same as current
Complete list of historical versions of study NCT02110069 on ClinicalTrials.gov Archive Site
  • Evaluation of Disease Response - Maintenance [ Time Frame: 6 months; 12 months ]
    Disease evaluation will be measured using a combination of quality of life assessments, clinical parameters, and radiologic images.
  • Number of serious and non serious adverse events - Maintenance [ Time Frame: 6 months; 12 months ]
    Serious adverse events and adverse events will be graded according to CTCAE v4.0. Adverse event rates will be calculated for both sirolimus and vincristine.
  • Change in the serum levels of KHE biomarkers [ Time Frame: Baseline, 2 months, 6 months, and 12 months ]
    The following KHE biomarkers will be evaluated vascular endothelial growth factor A, C, and D (VEGF-A, C, D_, IL-8 (interleukin), Pleiotrophin, IGF-1 (insulin-like growth factor), endothelin-1, thrombospondin and angiopoietin 1 and 2.
  • Identify genetic variants in drug metabolism enzymes. [ Time Frame: Baseline ]
    Single nucleotide polymorphism array analysis to obtain genetic information on variants in drug metabolism enzymes that affect sirolimus and vincristine metabolism.
Same as current
Not Provided
Not Provided
 
A Study to Compare Vincristine to Sirolimus for Treatment of High Risk Vascular Tumors
A Randomized Phase 2 Study of Vincristine Versus Sirolimus to Treat High Risk Kaposiform Hemangioendothelioma (KHE).

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)

Kaposiform hemangioendotheliomas (KHE) are extremely rare life threatening tumors which can be associated with Kasabach-Merritt Phenomenon consisting of profound thrombocytopenia and hypofibrinogenemia causing a significant risk of bleeding and an associated mortality rate as high as 20% to 30%. Despite the severity of potential complications, we lack uniform guidelines for the treatment and response to treatment of children and young adults with these tumors. KHE patients have been treated with a multitude of aggressive drug regimens without prospective evaluation of response or safety. Presently, vincristine is considered the standard of practice. We have treated a subset of these patients on study SIR-DA-0901 (FDA Grant# 5RO1FD003712-01). This study is a phase II trial assessing the efficacy and safety of sirolimus for the treatment of complicated vascular anomalies. Although the numbers are small, the response has been extremely promising with excellent tolerability. There is pre-clinical and clinical data supporting the essential regulatory function of the PI3 kinase/AKT/mTOR pathway in vascular growth and organization which suggests a therapeutic target for patients with complicated vascular anomalies. The overall goal of this trial is to objectively assess the efficacy of sirolimus compared to vincristine for the treatment of patients with high risk KHE.

Hypothesis: Sirolimus treatment for children and young adults with Kaposiform hemangioendotheliomas will be more effective than vincristine, assessed by time to response in an induction period and provide equivalent safety parameters.

Study Rationale We propose a multi-center, phase II trial with participation from 8 sites. The study will consist of two phases. The first of these is an initial induction phase in which vincristine and steroids will be compared to sirolimus and steroids. Response in the induction phase will be assessed as time to hematologic response. At the end of induction phase, cross over can occur if there is failure to respond. Part 2 is a maintenance phase which will be 1 year in length. Continued safety and efficacy data will be collected during maintenance and there will be cross over at any time for patients who lose their response following induction. Failure will be defined as worsening of hematological parameters on two separate laboratory evaluations at any time during maintenance or if they meet the definition of progressive disease following response assessments. Formal response in maintenance will be evaluated by imaging studies, functional assessment, and quality of life as per study SIR-DA-0901. Present therapies are very limited and new therapies are desperately needed for this devastating disease. Based on our preliminary data, there is a very good rationale for sirolimus therapy in KHE patients and so a phase II trial is urgently needed to determine if this therapy is to become the new standard of care for KHE patients.

Our secondary aims will be addressing biomarker analysis. There are limited studies describing the biology of these tumors. Per study SIR-DA-0901 there is some preliminary data indicating the importance of VEGF-C and other upregulated markers in the mTor pathway. This needs to be further investigated especially in KHE patients. Furthermore there are no clear objective measurements to determine response data.

Interventional
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Kaposiform Hemangioendothelioma (KHE)
  • Kasabach-Merritt Syndrome
  • Tufted Angioma
  • Drug: Vincristine
    Vincristine dose dependent upon weight. Weekly for 2 weeks (Induction); Weekly 2 months; every 2 weeks for next 5 months; every 3 weeks for 5 months (Maintenance)
    Other Names:
    • Oncovin
    • Vincasar® PFS
    • Vincrex
  • Drug: Sirolimus
    Continuous dosing to maintain trough level of 10-15ng/ml.
    Other Name: Rapamune
  • Active Comparator: Vincristine

    Induction phase: participants assigned to vincristine will receive vincristine weekly at a dose of 0.05mg/kd/dose IV (for participants less than 10kg) or a dose of 1.5 mg/m2/dose (for participants greater than 10kg).

    Maintenance: if participants continue to receive vincristine weekly for 2 months, every 2 weeks for 5 months and every 3 weeks for 5 months.

    Intervention: Drug: Vincristine
  • Experimental: Sirolimus

    Sirolimus will be administered at a dose of 0.8mg/m2/dose twice a day on a continuous dosing schedule throughout the trial for participants randomized to Sirolimus or for participants who fail vincristine may cross-over to the sirolimus arm.

    Sirolimus trough levels will be maintained between 10-15 ng/ml.

    Intervention: Drug: Sirolimus
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
50
December 2026
June 2021   (Final data collection date for primary outcome measure)

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.
Sexes Eligible for Study: All
up to 31 Years   (Child, Adult)
No
Contact: Denise Adams, MD 617-919-1761 denise.adams@childrens.harvard.edu
Contact: Yvonne Sheldon, RN, BSN 617-919-6299 yvonne.sheldon@childrens.harvard.edu
United States
 
 
NCT02110069
SIR-DA-1202
1R01FD004363-01A1 ( U.S. FDA Grant/Contract )
2013-2339 ( Other Identifier: CCHMC IRB )
Yes
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Plan to Share IPD: Undecided
Denise Martin Adams, Boston Children's Hospital
Boston Children’s Hospital
Pfizer
Principal Investigator: Denise Adams, MD Boston Children’s Hospital
Boston Children’s Hospital
July 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP