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Health Economics Evaluation of Percutaneous Vertebroplasty Compared to Radiation Therapy in Patients With Painful Spine Metastases. (Radiointer)

Primary Purpose

Spine Metastases

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
External radiotherapy
Percutaneous vertebroplasty
Sponsored by
Centre Leon Berard
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spine Metastases focused on measuring Health economics, Percutaneous vertebroplasty, Radiation therapy, Painful spine metastases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years at the day of consenting to the study
  • Patient with at least a painful spine metastasis confirmed by MRI / CT scan,
  • Localized pain at the lesion ≥ 4 (VAS),
  • Bone axial metastasis localised on ≤ 6 different vertebrae,
  • Histologically established diagnosis of cancer (lung, kidney, breast, prostate, melanoma, soft tissue sarcomas) other than hematologic malignancy, myeloma, brain tumor, germ cell tumor and bone sarcomas
  • ECOG performance status 0 to 2 (Appendix 2)
  • Minimum life expectancy of 6 months (Tokuhashi score > 8 )
  • Ability to understand and willingness for follow-up visits.
  • Covered by a medical insurance
  • Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrolment

Exclusion Criteria:

  • Solitary metastasis
  • SBRT indication
  • Contra-indication to vertebroplasty
  • Previous radiotherapy for pain management in the same area.
  • Patient unable to lie prone
  • Neurological deficit due to spinal cord compression,
  • Active infection,
  • Bleeding risk (platelets < 50000 and PTT > 1.5*ULN),
  • Risk of vertebral collapse (SINS score ≥ 13),
  • Impossible follow-up for social, geographical, familial or psychological reasons,
  • Patient deprived of freedom,
  • Patient enrolled in another experimental surgical trial, with therapeutic endpoint,
  • Pregnant or breastfeeding women,Pregnant or breastfeeding women (mandatory negative serum or urinary pregnancy test at study entry for all women of childbearing potential

Sites / Locations

  • Institut Bergonié
  • Centre Leon Berard
  • HCL- Hopital Edouard Herriot
  • Centre Antoine Lacassagne
  • Institut Curie
  • Centre Paul Strauss
  • Institut Gustave Roussy

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Arm A

Arm B

Arm Description

Percutaneous vertebroplasty

External radiotherapy

Outcomes

Primary Outcome Measures

Health economics evaluation
To perform a cost-utility analysis in order to provide recommendations to French decision-makers on the treatment of patients with painful spine metastases. Incremental cost-effectiveness ratio expressed in cost per quality adjusted life year (QALY) gained

Secondary Outcome Measures

Budget impact analysis of vertebroplasty
Cost-assessment, Quality of life (EQ-5D) Quality adjusted life year,

Full Information

First Posted
June 24, 2014
Last Updated
January 9, 2017
Sponsor
Centre Leon Berard
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1. Study Identification

Unique Protocol Identification Number
NCT02174107
Brief Title
Health Economics Evaluation of Percutaneous Vertebroplasty Compared to Radiation Therapy in Patients With Painful Spine Metastases.
Acronym
Radiointer
Official Title
Health Economics Evaluation of Percutaneous Vertebroplasty Compared to Radiation Therapy in Patients With Painful Spine Metastases.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Terminated
Why Stopped
recruitment issues due to feasability issues in centers
Study Start Date
April 2015 (undefined)
Primary Completion Date
April 2018 (Anticipated)
Study Completion Date
April 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Leon Berard

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate cost-utility analysis in order to provide recommendations to French decision-makers between vertebroplasty and radiation therapy in Bone spine metastases. Indeed, radiation therapy is often advocated a systematic way. The object of this study would be to expand the use of vertebroplasty. Moreover, this study assess to the strategy impact on the pain control reduction and functional preservation. In fact, analgesic effect is achieved differently depending on the procedure used.Eligible patients will be recruited and registered consecutively. Patients will be randomly, This is a health-economic multicenter, prospective, randomized with stratification according to number of vertebrae to treat (1-3 vertebrae vs 4-6 vertebrae) and center : Arm A: Percutaneous vertebroplasty Arm B: External radiotherapy This is an open-label study. The expected total study period is 2.5 years (enrolment: 2 years, patient follow-up: 6 months). A total number of 304 patients with spine metastases will be recruited (152 patients/arm).
Detailed Description
Bone is the most common site for metastasis. In breast and prostate cancers, 70% of patients dying of their cancer have evidence of metastatic bone disease [Coleman, 2006]. Depending on their localization, bone metastases can have debilitating consequences resulting in considerable morbidity and complex demands on health care resources. Bone spine metastases are the most frequent site observed in patients with cancer of the lung, prostate, breast and hemopoetic organs. The occurrence of spinal metastases in patients with advanced cancer can cause significant morbidity, with pain and/or neurological deficit adversely affecting the patients' quality of life. Interventional radiology takes a large place in the treatment of bone metastases. Currently, vertebroplasty appears as the most satisfactory technique for stabilization of spine metastases offering a significant improvement of the quality of life. The analgesic effect is achieved very rapidly, i.e. usually within 24 hours post-procedure. Based on several publications, around 90% of patients reported rapid pain relief following vertebroplasty with 60 to 70% of complete pain relief [Mendel, 2009]. Radiotherapy also plays a very important role in the palliative treatment of the metastatic bone. Radiotherapy is effective and well tolerated. A reduction of the pain is noticed for 70 to 80 % of the patients and begins one or two weeks after the treatment. In all, the radiotherapy increases the quality of life of the patients and can reduce the intake of analgesics [Lutz, 2011]. In a lot of cases, vertebroplasty or radiotherapy can both be performed for a same painful patient (the National Institute for Health and Clinical Excellence (NICE) approved the use of vertebroplasty for patients with spinal metastases in November 2008). Radiotherapy remains the gold-standard treatment. However, vertebroplasty could be less costly and more effective compare to radiotherapy. In fact, the superiority of vertebroplasty has been demonstrated at least in the acute post-therapeutic period with (i) more rapid autonomy recovery, (ii) reduction of antalgic intakes, and potentially less side-effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spine Metastases
Keywords
Health economics, Percutaneous vertebroplasty, Radiation therapy, Painful spine metastases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm A
Arm Type
Experimental
Arm Description
Percutaneous vertebroplasty
Arm Title
Arm B
Arm Type
Experimental
Arm Description
External radiotherapy
Intervention Type
Radiation
Intervention Name(s)
External radiotherapy
Intervention Description
The radiation technique used for each patient will be based on local clinical practices and on number of vertebae to treat between 1*8 Gy; 5*4 Gy and 10*3 Gy
Intervention Type
Procedure
Intervention Name(s)
Percutaneous vertebroplasty
Other Intervention Name(s)
Vertebroplasty
Primary Outcome Measure Information:
Title
Health economics evaluation
Description
To perform a cost-utility analysis in order to provide recommendations to French decision-makers on the treatment of patients with painful spine metastases. Incremental cost-effectiveness ratio expressed in cost per quality adjusted life year (QALY) gained
Time Frame
6 months after the end ot treatment
Secondary Outcome Measure Information:
Title
Budget impact analysis of vertebroplasty
Description
Cost-assessment, Quality of life (EQ-5D) Quality adjusted life year,
Time Frame
6 months after the end of treatment
Other Pre-specified Outcome Measures:
Title
Assessment of pain reduction
Description
Visual analogue scale: VAS
Time Frame
3 weeks, 3 months and 6 months after the end of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years at the day of consenting to the study Patient with at least a painful spine metastasis confirmed by MRI / CT scan, Localized pain at the lesion ≥ 4 (VAS), Bone axial metastasis localised on ≤ 6 different vertebrae, Histologically established diagnosis of cancer (lung, kidney, breast, prostate, melanoma, soft tissue sarcomas) other than hematologic malignancy, myeloma, brain tumor, germ cell tumor and bone sarcomas ECOG performance status 0 to 2 (Appendix 2) Minimum life expectancy of 6 months (Tokuhashi score > 8 ) Ability to understand and willingness for follow-up visits. Covered by a medical insurance Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrolment Exclusion Criteria: Solitary metastasis SBRT indication Contra-indication to vertebroplasty Previous radiotherapy for pain management in the same area. Patient unable to lie prone Neurological deficit due to spinal cord compression, Active infection, Bleeding risk (platelets < 50000 and PTT > 1.5*ULN), Risk of vertebral collapse (SINS score ≥ 13), Impossible follow-up for social, geographical, familial or psychological reasons, Patient deprived of freedom, Patient enrolled in another experimental surgical trial, with therapeutic endpoint, Pregnant or breastfeeding women,Pregnant or breastfeeding women (mandatory negative serum or urinary pregnancy test at study entry for all women of childbearing potential
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bertrand BR RICHIOUD, MD
Organizational Affiliation
Center Leon Berard
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Bergonié
City
Bordeaux
Country
France
Facility Name
Centre Leon Berard
City
Lyon
Country
France
Facility Name
HCL- Hopital Edouard Herriot
City
Lyon
Country
France
Facility Name
Centre Antoine Lacassagne
City
Nice
Country
France
Facility Name
Institut Curie
City
Paris
Country
France
Facility Name
Centre Paul Strauss
City
Strasbourg
Country
France
Facility Name
Institut Gustave Roussy
City
Villejuif
Country
France

12. IPD Sharing Statement

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Health Economics Evaluation of Percutaneous Vertebroplasty Compared to Radiation Therapy in Patients With Painful Spine Metastases.

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