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Intensity-modulated Radiotherapy With Integrated-boost in Patients With Spinal Bone Metastases (IRON-2)

Primary Purpose

Vertebral Bony Metastases

Status
Unknown status
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
A
B
C
D
Sponsored by
Heidelberg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vertebral Bony Metastases focused on measuring Palliative radiotherapy, Bone metastases

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a histologically confirmed tumor diagnosis, with secondarily diagnosed solitary/multiple metastatic spinal bone metastases
  • Indication for RT of the bone metastasis
  • Age: between 18 and 80 years
  • Karnofsky performance score ≥ 70
  • Signed Declaration of Informed Consent
  • Bisphosphonate therapy

Exclusion Criteria:

  • Significant neurological or psychiatric disorders, including dementia and epileptic seizures
  • Lacking or diminished legal capacity
  • foregoing radiotherapy in the planned RT area
  • Any medical of psychological condition that the study director considers a preventive factor for the patient's ability to complete the study or to adequately understand the scope of the study and to give his/her consent

Sites / Locations

  • Dept of Radiation Oncology, University of Heidelberg, Germany

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

A

B

C

D

Arm Description

Intensity modulated radiotherapy (IMRT) 30Gy in 10 fractions

Intensity modulated radiotherapy (IMRT) 30Gy in 10 fractions with an SIB with 40 Gy in 10 fractions to the metastasis

Intensity modulated radiotherapy (IMRT) 20Gy in 5 fractions

Intensity modulated radiotherapy (IMRT) 20Gy in 5 fractions with an SIB with 30 Gy in 5 fractions to the metastasis

Outcomes

Primary Outcome Measures

local control
local control as bone density is assessed 12 weeks post completion of radiotherapy using follow-up CT scan of the spine

Secondary Outcome Measures

progression-free survival (PFS)
PFS is assessed 2 years post completion of radiotherapy
pain reduction
pain is evaluated using the VAS pain scale (0-100 points) at completion and 12/ 24 weeks post completion of radiation
Quality of life
Quality of life is assessed using the EORTC BM22 questionnaire at 12 and 24 weeks post completion of treatment
Fatigue
Fatigue is assessed using the EORTC FA13 questionnaire

Full Information

First Posted
July 12, 2016
Last Updated
July 12, 2016
Sponsor
Heidelberg University
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1. Study Identification

Unique Protocol Identification Number
NCT02832765
Brief Title
Intensity-modulated Radiotherapy With Integrated-boost in Patients With Spinal Bone Metastases
Acronym
IRON-2
Official Title
Intensity-modulated Radiotherapy With Integrated-boost in Patients With Spinal Bone Metastases
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Unknown status
Study Start Date
September 2016 (undefined)
Primary Completion Date
February 2018 (Anticipated)
Study Completion Date
February 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Heidelberg University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary goal of the study is to determine the local control-rate after radiotherapy (RT) with and without simultaneous integrated boost (SIB) concepts in patients with bone metastases of the spine. Further study objectives are survival, and clinical parameters such as pain, quality of life (QoL) and fatigue. We expect an improvement in local control and consecutively an increased re-sclerotization of the bone metastasis due to a higher biological dose in the tumor area. Therefore patients could benefit in quality-of-life, pain relief and mobility.
Detailed Description
The vertebral column is the main localization of bone metastases and is where they frequently indicate an advanced stage of a malignant primary disease [1, 2]. Two thirds of all patients with tumors are estimated to develop bone metastases in the course of their disease [3]. Spinal bone metastases are of central impact for patients in a palliative setting. The clinical symptoms include pain at rest and under exercise but also impaired activity of daily life, the risk of pathological fractures, and neurological deficits. Local control is the essential factor for stability of the vertebral body of patients with spinal bone metastases. In regard to re-calcification of former osteolytic lesions, palliative radiotherapy (RT) represents an effective treatment option [4]. The most common schedule was specified as 30 Gy in 10 fractions. Stereotactic body radiation therapy (SBRT) using intensity-modulated radiotherapy (IMRT) can be a safe modality for treating spinal metastasis with enhanced targeting accuracy [5]. Secondly, IMRT to the spine was well tolerated (especially in the spinal cord), had no significant late toxicities, and spared other organs at risk simultaneously [6]. The main problem of the standard schedule is the limited dose application to the metastasis due to organ at risk myelon. Therefore, the aims of this study is to apply a high biological dose in the tumor region and to achieve an improved result related to local control for palliative patients with painful spinal bone metastases. Secondly, the aim is to evaluate QoL, fatigue, and survival of three different RT-techniques. To the best of our knowledge, no comparable randomized study has been described in the literature so far.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vertebral Bony Metastases
Keywords
Palliative radiotherapy, Bone metastases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Intensity modulated radiotherapy (IMRT) 30Gy in 10 fractions
Arm Title
B
Arm Type
Experimental
Arm Description
Intensity modulated radiotherapy (IMRT) 30Gy in 10 fractions with an SIB with 40 Gy in 10 fractions to the metastasis
Arm Title
C
Arm Type
Experimental
Arm Description
Intensity modulated radiotherapy (IMRT) 20Gy in 5 fractions
Arm Title
D
Arm Type
Experimental
Arm Description
Intensity modulated radiotherapy (IMRT) 20Gy in 5 fractions with an SIB with 30 Gy in 5 fractions to the metastasis
Intervention Type
Radiation
Intervention Name(s)
A
Intervention Description
Intensity modulated radiotherapy (IMRT) 30Gy in 10 fractions of the involved spinal bone metastases
Intervention Type
Radiation
Intervention Name(s)
B
Intervention Description
Intensity modulated radiotherapy (IMRT) 30Gy in 10 fractions with an SIB with 40 Gy in 10 fractions to the metastasis of the involved spinal bone metastases
Intervention Type
Radiation
Intervention Name(s)
C
Intervention Description
Intensity modulated radiotherapy (IMRT) 20Gy in 5 fractions of the involved spinal bone metastases
Intervention Type
Radiation
Intervention Name(s)
D
Intervention Description
Intensity modulated radiotherapy (IMRT) 20Gy in 5 fractions with an SIB with 30 Gy in 5 fractions to the metastasis of the involved spinal bone metastases
Primary Outcome Measure Information:
Title
local control
Description
local control as bone density is assessed 12 weeks post completion of radiotherapy using follow-up CT scan of the spine
Time Frame
3 months after RT
Secondary Outcome Measure Information:
Title
progression-free survival (PFS)
Description
PFS is assessed 2 years post completion of radiotherapy
Time Frame
2 years post completion of radiotherapy
Title
pain reduction
Description
pain is evaluated using the VAS pain scale (0-100 points) at completion and 12/ 24 weeks post completion of radiation
Time Frame
end of treatment, 12 and 24 weeks post completion of radiotherapy
Title
Quality of life
Description
Quality of life is assessed using the EORTC BM22 questionnaire at 12 and 24 weeks post completion of treatment
Time Frame
12 and 24 weeks post completion of therapy
Title
Fatigue
Description
Fatigue is assessed using the EORTC FA13 questionnaire
Time Frame
12 and 24 weeks post completion of therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a histologically confirmed tumor diagnosis, with secondarily diagnosed solitary/multiple metastatic spinal bone metastases Indication for RT of the bone metastasis Age: between 18 and 80 years Karnofsky performance score ≥ 70 Signed Declaration of Informed Consent Bisphosphonate therapy Exclusion Criteria: Significant neurological or psychiatric disorders, including dementia and epileptic seizures Lacking or diminished legal capacity foregoing radiotherapy in the planned RT area Any medical of psychological condition that the study director considers a preventive factor for the patient's ability to complete the study or to adequately understand the scope of the study and to give his/her consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Harald Rief, MD, PhD
Email
harald.rief@med.uni-heidelberg.de
First Name & Middle Initial & Last Name or Official Title & Degree
Jürgen Debus, MD, PhD
Email
juergen.debus@med.uni-heidelberg.de
Facility Information:
Facility Name
Dept of Radiation Oncology, University of Heidelberg, Germany
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24890347
Citation
Ryu S, Pugh SL, Gerszten PC, Yin FF, Timmerman RD, Hitchcock YJ, Movsas B, Kanner AA, Berk LB, Followill DS, Kachnic LA. RTOG 0631 phase 2/3 study of image guided stereotactic radiosurgery for localized (1-3) spine metastases: phase 2 results. Pract Radiat Oncol. 2014 Mar-Apr;4(2):76-81. doi: 10.1016/j.prro.2013.05.001. Epub 2013 Jun 4.
Results Reference
result
PubMed Identifier
22172095
Citation
Guckenberger M, Sweeney RA, Flickinger JC, Gerszten PC, Kersh R, Sheehan J, Sahgal A. Clinical practice of image-guided spine radiosurgery--results from an international research consortium. Radiat Oncol. 2011 Dec 15;6:172. doi: 10.1186/1748-717X-6-172.
Results Reference
result
PubMed Identifier
23101946
Citation
Katsoulakis E, Riaz N, Cox B, Mechalakos J, Zatcky J, Bilsky M, Yamada Y. Delivering a third course of radiation to spine metastases using image-guided, intensity-modulated radiation therapy. J Neurosurg Spine. 2013 Jan;18(1):63-8. doi: 10.3171/2012.9.SPINE12433. Epub 2012 Oct 26.
Results Reference
result
PubMed Identifier
23052695
Citation
Chung Y, Yoon HI, Kim JH, Nam KC, Koom WS. Is helical tomotherapy accurate and safe enough for spine stereotactic body radiotherapy? J Cancer Res Clin Oncol. 2013 Feb;139(2):243-8. doi: 10.1007/s00432-012-1321-0. Epub 2012 Oct 2.
Results Reference
result
PubMed Identifier
29357902
Citation
Sprave T, Welte SE, Bruckner T, Forster R, Bostel T, Schlampp I, Nicolay NH, Debus J, Rief H. Intensity-modulated radiotherapy with integrated-boost in patients with bone metastasis of the spine: study protocol for a randomized controlled trial. Trials. 2018 Jan 22;19(1):59. doi: 10.1186/s13063-018-2452-7.
Results Reference
derived

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Intensity-modulated Radiotherapy With Integrated-boost in Patients With Spinal Bone Metastases

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