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Endostatin Study for Patients With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors (Endostatin)

Primary Purpose

Vestibular Schwannoma, Neurofibromatosis Type 2

Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Endostatin
Sponsored by
Beijing Tiantan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vestibular Schwannoma focused on measuring Neurofibromatosis Type 2, Vestibular Schwannoma, Other NF2-related tumors

Eligibility Criteria

16 Years - 30 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1)Patients must be at the age of 16-30
  • 2)Patients must meet the diagnostic criteria for NF2, with bilateral acoustic neuroma and other central nervous system tumors
  • 3)Patients must not be treated with other drugs or radiation therapy recently
  • 4)Patients should live in Beijing or nearby and can be treated in hospital
  • 5)Patients must be healthy and not be seriously allergic with biological agents
  • 6)Patients must join the clinical trial voluntarily, with good compliance, cooperate with the researchers well, sign a written informed consent.

Exclusion Criteria:

  • 1)Treated with other drugs, surgery or radiation therapy recently
  • 2)Brainstem is compressed seriously, with hydrocephalus, need to be treated with surgery in short time
  • 3)Being pregnant or try to get pregnant, lactating women
  • 4)With acute or chronic infectious diseases
  • 5)With heart diseases, cardiac dysfunction or abnormal ECG
  • 6)With uncontrolled neural or mental diseases, poor compliance
  • 7)Not available for enhanced MRI
  • 8)Take part in any other clinical trial
  • 9)With other conditions that are considered not suitable for this clinical trial.

Sites / Locations

  • Beijing Tiantan Hospital Affiliated to Capital Medical University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Endostatin,treatment effect evaluation

Arm Description

Patients receive continuous intravenous Endostatin drug pumping during the course of treatment. The drug dosage is 7.5mg/m2/d. Every course of treatment lasts three months. Patients are designed to receive total three courses of treatment if there is no disease progression. The interval between two courses is one month.

Outcomes

Primary Outcome Measures

Change from Baseline in volume of tumour after every course of the treatment
Patients in this clinical trial would receive MRI test to evaluate the volume of tumour after every course of the treatment.

Secondary Outcome Measures

Change from Baseline in hearing ability after every course of the treatment
Patients' hearing ability would be tested after every course of the treatment.

Full Information

First Posted
March 26, 2014
Last Updated
February 7, 2017
Sponsor
Beijing Tiantan Hospital
Collaborators
Shandong Simcere-Medgenn Bio-pharmaceutical Co., Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT02104323
Brief Title
Endostatin Study for Patients With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors
Acronym
Endostatin
Official Title
Recombinant Human Endostatin Injection Study for Patients With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors by Continuous Intravenous Pumping
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Tiantan Hospital
Collaborators
Shandong Simcere-Medgenn Bio-pharmaceutical Co., Ltd

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
1)Preliminarily evaluate the treatment effect of continuous vein injection of recombinant human endostatin on NF2; 2)Preliminarily evaluate the safety and the patient's tolerance of the treatment of endostatin; 3)Provide an objective basis for an enlarged randomized double-blind trial.
Detailed Description
Neurofibromatosis type 2 (NF2) is a hereditary tumor predisposition syndrome caused by mutations in the NF2 tumor suppressor gene. Individuals with NF2 have a higher likelihood to develop multiple nervous system tumors, including schwannomas, meningiomas, and ependymomas. The hallmark of NF2 is bilateral vestibular schwannomas. Historically, most NF2 patients experience complete hearing loss either from tumor progression or after treatment of the tumors with surgery or radiation. Effective treatments are urgently needed for NF2 patients with progressive hearing loss because hearing loss is associated with impairment in social, emotional,and communication function and with increased depression. Previous studies of NF2 patients treated with bevacizumab suggested that inhibition of vascular endothelial growth factor (VEGF) could result in hearing improvement and reduction in tumor size.Recombinant human endostatin can inhibit the formation of blood vessels by inhibiting the migration of vascular endothelial cells .In this way, endostatin can inhibit the nutrition of the tumor and decrease the tumor's growth and metastasis. In vitro tests, endostatin can inhibit the cell migration and Tube formation of the microvascular endothelial cell line HHEC. Besides, it can inhibit blood vessels' formation of the chicken embryo sac membrane. Based on these studies, we perform this clinical trial to known the treatment effect and tolerability of endostatin on NF2.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Schwannoma, Neurofibromatosis Type 2
Keywords
Neurofibromatosis Type 2, Vestibular Schwannoma, Other NF2-related tumors

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Endostatin,treatment effect evaluation
Arm Type
Experimental
Arm Description
Patients receive continuous intravenous Endostatin drug pumping during the course of treatment. The drug dosage is 7.5mg/m2/d. Every course of treatment lasts three months. Patients are designed to receive total three courses of treatment if there is no disease progression. The interval between two courses is one month.
Intervention Type
Drug
Intervention Name(s)
Endostatin
Other Intervention Name(s)
Recombinant Human Endostatin
Intervention Description
Method of drug administration:continuous intravenous pumping; Dosage: 7.5mg/m2/d; Course of treatment: 3 months;Total three treatment courses.
Primary Outcome Measure Information:
Title
Change from Baseline in volume of tumour after every course of the treatment
Description
Patients in this clinical trial would receive MRI test to evaluate the volume of tumour after every course of the treatment.
Time Frame
Baseline,Month 3,Month 7,Month 11
Secondary Outcome Measure Information:
Title
Change from Baseline in hearing ability after every course of the treatment
Description
Patients' hearing ability would be tested after every course of the treatment.
Time Frame
Baseline,Month 3,Month 7,Month 11
Other Pre-specified Outcome Measures:
Title
Change from baseline in QOL(quality of life) score after every course of the treatment
Description
Patients' QOL(quality of life) would be evaluated after every course of the treatment.
Time Frame
Baseline,Month 3,Month 7,Month 11

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1)Patients must be at the age of 16-30 2)Patients must meet the diagnostic criteria for NF2, with bilateral acoustic neuroma and other central nervous system tumors 3)Patients must not be treated with other drugs or radiation therapy recently 4)Patients should live in Beijing or nearby and can be treated in hospital 5)Patients must be healthy and not be seriously allergic with biological agents 6)Patients must join the clinical trial voluntarily, with good compliance, cooperate with the researchers well, sign a written informed consent. Exclusion Criteria: 1)Treated with other drugs, surgery or radiation therapy recently 2)Brainstem is compressed seriously, with hydrocephalus, need to be treated with surgery in short time 3)Being pregnant or try to get pregnant, lactating women 4)With acute or chronic infectious diseases 5)With heart diseases, cardiac dysfunction or abnormal ECG 6)With uncontrolled neural or mental diseases, poor compliance 7)Not available for enhanced MRI 8)Take part in any other clinical trial 9)With other conditions that are considered not suitable for this clinical trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pinan Liu
Organizational Affiliation
Beijing Tiantan Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Fu Zhao
Organizational Affiliation
Beijing Neurosurgical Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Tiantan Hospital Affiliated to Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100050
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22805104
Citation
Plotkin SR, Merker VL, Halpin C, Jennings D, McKenna MJ, Harris GJ, Barker FG 2nd. Bevacizumab for progressive vestibular schwannoma in neurofibromatosis type 2: a retrospective review of 31 patients. Otol Neurotol. 2012 Aug;33(6):1046-52. doi: 10.1097/MAO.0b013e31825e73f5.
Results Reference
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PubMed Identifier
19587327
Citation
Plotkin SR, Stemmer-Rachamimov AO, Barker FG 2nd, Halpin C, Padera TP, Tyrrell A, Sorensen AG, Jain RK, di Tomaso E. Hearing improvement after bevacizumab in patients with neurofibromatosis type 2. N Engl J Med. 2009 Jul 23;361(4):358-67. doi: 10.1056/NEJMoa0902579. Epub 2009 Jul 8.
Results Reference
background
PubMed Identifier
23555840
Citation
Nunes FP, Merker VL, Jennings D, Caruso PA, di Tomaso E, Muzikansky A, Barker FG 2nd, Stemmer-Rachamimov A, Plotkin SR. Bevacizumab treatment for meningiomas in NF2: a retrospective analysis of 15 patients. PLoS One. 2013;8(3):e59941. doi: 10.1371/journal.pone.0059941. Epub 2013 Mar 21.
Results Reference
background
PubMed Identifier
24249803
Citation
Plotkin SR, Ardern-Holmes SL, Barker FG 2nd, Blakeley JO, Evans DG, Ferner RE, Hadlock TA, Halpin C; REiNS International Collaboration. Hearing and facial function outcomes for neurofibromatosis 2 clinical trials. Neurology. 2013 Nov 19;81(21 Suppl 1):S25-32. doi: 10.1212/01.wnl.0000435746.02780.f6.
Results Reference
background
PubMed Identifier
20150363
Citation
Mautner VF, Nguyen R, Kutta H, Fuensterer C, Bokemeyer C, Hagel C, Friedrich RE, Panse J. Bevacizumab induces regression of vestibular schwannomas in patients with neurofibromatosis type 2. Neuro Oncol. 2010 Jan;12(1):14-8. doi: 10.1093/neuonc/nop010. Epub 2009 Oct 20.
Results Reference
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Endostatin Study for Patients With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors

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