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CyberKnife Based Hypofractionated Radiotherapy for Vertebral Hemangiomas (CKHRTVH)

Primary Purpose

Hemangioma of Vertebral Column

Status
Unknown status
Phase
Phase 3
Locations
Poland
Study Type
Interventional
Intervention
Cybernetic microradiosurgery
Conventional radiotherapy
Sponsored by
Maria Sklodowska-Curie National Research Institute of Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemangioma of Vertebral Column focused on measuring vertebral hemangioma, conventional radiotherapy, Cyber Knife radiotherapy, randomized trial, radioablation

Eligibility Criteria

25 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Confirmed vertebral hemangioma ,
  2. Lesion visible in CT and MR
  3. Pain located in area of the lesion
  4. Informed consent for participation in the study and for radiotherapy in interested area

Exclusion Criteria:

  1. Any previous radiotherapy in region of treated hemangioma
  2. Spinal damage or disease that may be associated with an increased radiosensitivity
  3. The coexistence of the vertebral morphological changes at the level of hemangioma causing pressure on the nerve roots and / or spinal cord causing pain located in that area
  4. Neurological deficits caused by the presence of hemangioma (patients should be considered for surgery)
  5. Contradictions for MRI
  6. Lack of informed consent.

Sites / Locations

  • Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology Gliwice BranchRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Cybernetic microradiosurgery

Conventional radiotherapy

Arm Description

Hypofractionated microradiosurgery using Cyber Knife to the vertebral hemangioma to the total dose of 25 Gy in 5.0 Gy per fraction, 2 or 3 days a week over the period of 2 weeks,

Conventionally fractionated external beam conformal radiotherapy to the vertebral hemangioma to the total dose of 36 Gy in 2.0 Gy per fraction, 5 days a week over the period of 3,5 weeks,

Outcomes

Primary Outcome Measures

Analgetic effect
rate of pain relief

Secondary Outcome Measures

Identification of radiologic prognostic and predictal factors of response to external beam radiotherapy (radiosurgery compared to conventional)
Identification of biochemical and physical prognostic factors of response to external beam radiotherapy (radiosurgery compared to conventional)

Full Information

First Posted
January 4, 2015
Last Updated
January 4, 2015
Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology
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1. Study Identification

Unique Protocol Identification Number
NCT02332408
Brief Title
CyberKnife Based Hypofractionated Radiotherapy for Vertebral Hemangiomas
Acronym
CKHRTVH
Official Title
CyberKnife Based Hypofractionated Radiotherapy Versus Conventional Linac Based Radiotherapy for Painful Vertebral Hemangiomas - Controlled Randomized Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2014 (undefined)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
September 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Clinical objective of the study is to compare the analgesic effect, toxicity and pathologic effect in the tumors of two radiotherapy schedules used for patients suffering from painful vertebral haemangiomas
Detailed Description
Hemangiomas are frequent vertebral lesions (12% of the whole human population) but only 1% displays any clinical symptoms . The most common symptom is local pain, usually non responding for non-steroid anti-inflammatory drugs. Radiation therapy usually does not result calcification or the tumor regression, but significantly reduces the pain intensity or eliminates it. Currently, the most common RT schedule is conventional radiotherapy using fraction dose (fd) of 2 Gy delivered to the total dose (TD) varying from36 Gy to 40 Gy. The results in pain reduction achieved after larger total doses are better that led us to use radioablative techniques. This procedure is associated with a probability of better analgesic effect and the good local effect (calcification and / or regression of laesion) with high safety of radiation delivery using tracking based cybernetic microradiosurgery (CyberKnife). The comparison of two modalities of radiation therapy (conventional [fd 2 Gy, TD 36 Gy] and hypofractionated [fd 5 Gy, TD 25 Gy]) used for treatment of painful vertebral hemangioma patients will be performed in the phase III randomized study. 80 patients will be enrolled in this study. All patients will be planned (RT) on the base of CT/MRI fusion. Patients will be controlled 1, 3, 6, 9, 12 months after treatment completion and, next every each 6 months. Pain relief, analgesics uptake, local effect (MRI and Technetium - 99m-labelled RBC(red blood cell) scintigraphy) and eventual toxicity will be checked during follow-up (FU).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemangioma of Vertebral Column
Keywords
vertebral hemangioma, conventional radiotherapy, Cyber Knife radiotherapy, randomized trial, radioablation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cybernetic microradiosurgery
Arm Type
Experimental
Arm Description
Hypofractionated microradiosurgery using Cyber Knife to the vertebral hemangioma to the total dose of 25 Gy in 5.0 Gy per fraction, 2 or 3 days a week over the period of 2 weeks,
Arm Title
Conventional radiotherapy
Arm Type
Active Comparator
Arm Description
Conventionally fractionated external beam conformal radiotherapy to the vertebral hemangioma to the total dose of 36 Gy in 2.0 Gy per fraction, 5 days a week over the period of 3,5 weeks,
Intervention Type
Radiation
Intervention Name(s)
Cybernetic microradiosurgery
Intervention Description
Cybernetic microradiosurgery (6MV) using tracking to TD 25Gy given in five fraction (5Gy p fr) two or three days a week, during 2 weeks
Intervention Type
Radiation
Intervention Name(s)
Conventional radiotherapy
Intervention Description
Conventionally fractionated linac based external beam radiation therapy - EBRT, (conformal or dynamic) to the TD of 36 Gy, in 2.0 Gy per fraction 5 days a week over the period of 3.5 weeks)
Primary Outcome Measure Information:
Title
Analgetic effect
Description
rate of pain relief
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Identification of radiologic prognostic and predictal factors of response to external beam radiotherapy (radiosurgery compared to conventional)
Time Frame
2 years
Title
Identification of biochemical and physical prognostic factors of response to external beam radiotherapy (radiosurgery compared to conventional)
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed vertebral hemangioma , Lesion visible in CT and MR Pain located in area of the lesion Informed consent for participation in the study and for radiotherapy in interested area Exclusion Criteria: Any previous radiotherapy in region of treated hemangioma Spinal damage or disease that may be associated with an increased radiosensitivity The coexistence of the vertebral morphological changes at the level of hemangioma causing pressure on the nerve roots and / or spinal cord causing pain located in that area Neurological deficits caused by the presence of hemangioma (patients should be considered for surgery) Contradictions for MRI Lack of informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Leszek Miszczyk, MD, PhD
Phone
0048322788001
Email
leszek@io.gliwice.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leszek Miszczyk, MD, PhD
Organizational Affiliation
Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice Branch, Gliwice, Poland
Official's Role
Study Director
Facility Information:
Facility Name
Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology Gliwice Branch
City
Gliwice
State/Province
Wybrzeze AK 15
ZIP/Postal Code
44-100
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Leszek MIszczyk, MD. PhD
Phone
+48322788001
Email
leszek@io.gliwice.pl
First Name & Middle Initial & Last Name & Degree
Leszek Miszczyk, MD, PhD
First Name & Middle Initial & Last Name & Degree
Grzegorz Wozniak, MD PhD
First Name & Middle Initial & Last Name & Degree
Aleksandra Napieralska, MD
First Name & Middle Initial & Last Name & Degree
Andrzej Tukiendorf, PhD
First Name & Middle Initial & Last Name & Degree
MIchał Gola, MD
First Name & Middle Initial & Last Name & Degree
Michał Kalemba, MD

12. IPD Sharing Statement

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CyberKnife Based Hypofractionated Radiotherapy for Vertebral Hemangiomas

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