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Optimization of Radiotherapy in Treatment of Painful Bone Metastasis (bone mets)

Primary Purpose

Pain, Bone Metastasis

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Radiotherapy
Radiotherapy
Radiotherapy
Radiotherapy
Sponsored by
International Atomic Energy Agency
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain focused on measuring single bone metastasis, multiple bone metastasis, pain relief, radiotherapy

Eligibility Criteria

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

Inclusion Criteria:

  • histological diagnosis of malignancy associated with radiological evidence of painful bone metastasis
  • If patients with two sites of pain requiring separate treatment are to be entered, the same randomized treatment option will be used for both sites, but response at each site will be scored and analyzed separately.
  • age > 18 years
  • anticipated remaining life of at least 12 weeks (3 months)
  • informed consent

Exclusion Criteria:

  • Primary histology myeloma
  • Sites of previous RT or previous radioisotope treatment
  • conditions or circumstances, which may interfere with treatment or follow-up
  • complicated bone metastasis (pathological fractures, metastatic spinal cord compression)

Sites / Locations

  • Centre Pierre et Marie Curie, Centre hospitalier universitaire Mustapha (CHU)
  • Irmandade de Santa Casa de Misericordia de Porto Alegre
  • Misr Oncology Center (MOC)
  • Tata Memorial Hospital
  • Institute of Oncology, University of Vilinius
  • Institute of Radiotherapy and Oncology
  • Instituto Nacional de Cancerología (INCAN)
  • Institute of Oncology and Radiology
  • Hospital Clinic Universidad de Barcelona
  • Hospital Son Dureta
  • Institut national de cancer Salah Azaiz
  • Mount Vernon Cancer Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Active Comparator

Experimental

Arm Label

Single Site Radiation 4Gy Fraction

Single Site Radiation 8Gy Fraction

Multiple Sites Radiation 8Gy Fraction

Multiple Sites Radiation 12Gy Fraction

Arm Description

4 Gy single fraction; mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks

8 Gy single fraction, mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks

8 Gy in a single fraction; retreatments > 4 weeks, using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy) ; second reirradiation with 8 Gy using local RT fields optional (at discretion of PI);

12 Gy in 4 fractions of 3 Gy in 2 consecutive days interfraction interval of a minimum of 6 hrs; retreatments > 4 weeks using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy); second reirradiation with 8 Gy using local RT fields optional (at discretion of PI) ;

Outcomes

Primary Outcome Measures

Pain Relief (response rate) at 4 weeks

Secondary Outcome Measures

Onset and Duration of Pain Relief in Responders
Toxicity
Quality of Life
Rates of Pathological Fractures and Spinal Cord Compression

Full Information

First Posted
January 25, 2008
Last Updated
August 6, 2013
Sponsor
International Atomic Energy Agency
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1. Study Identification

Unique Protocol Identification Number
NCT00610272
Brief Title
Optimization of Radiotherapy in Treatment of Painful Bone Metastasis
Acronym
bone mets
Official Title
Investigation of Optimal Radiotherapy Regimen and Type of Irradiation in Treatment of Painful Bone Metastasis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Atomic Energy Agency

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bone metastasis is one of the most frequent end complications of the cancer. Radiation therapy is the mainstay of treatment in this disease. Single fraction radiotherapy in both single and multiple bone metastasis is widely used, but optimization of the single dose fractionation is needed. Two different regimens of radiotherapy dose fractionation will be investigated in both single and multiple bone metastasis and endpoints will include pain relief as well as toxicity and quality of life.
Detailed Description
PROTOCOL SCHEMA Group A Treatment of single site of painful bone metastasis: Arm 1: 4 Gy single fraction; mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks Arm 2: 8 Gy single fraction, mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks Group B Treatment of multiple bone metastasis: lower hemibody radiotherapy (LHBI): Arm 3: 8 Gy in a single fraction; retreatments > 4 weeks, using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy) ; second reirradiation with 8 Gy using local RT fields optional (at discretion of PI); Arm 4: 12 Gy in 4 fractions of 3 Gy in 2 consecutive days interfraction interval of a minimum of 6 hrs; retreatments > 4 weeks using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy); second reirradiation with 8 Gy using local RT fields optional (at discretion of PI) ;

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Bone Metastasis
Keywords
single bone metastasis, multiple bone metastasis, pain relief, radiotherapy

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Single Site Radiation 4Gy Fraction
Arm Type
Experimental
Arm Description
4 Gy single fraction; mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks
Arm Title
Single Site Radiation 8Gy Fraction
Arm Type
Active Comparator
Arm Description
8 Gy single fraction, mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks
Arm Title
Multiple Sites Radiation 8Gy Fraction
Arm Type
Active Comparator
Arm Description
8 Gy in a single fraction; retreatments > 4 weeks, using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy) ; second reirradiation with 8 Gy using local RT fields optional (at discretion of PI);
Arm Title
Multiple Sites Radiation 12Gy Fraction
Arm Type
Experimental
Arm Description
12 Gy in 4 fractions of 3 Gy in 2 consecutive days interfraction interval of a minimum of 6 hrs; retreatments > 4 weeks using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy); second reirradiation with 8 Gy using local RT fields optional (at discretion of PI) ;
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
4 Gy single fraction; mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
8 Gy single fraction, mandate first retreatment if moderate or severe pain persists or recurs (as measured by categorical pain scale or VAS greater than 50 mm), >4 weeks after initial RT) retreat with 8 Gy single fraction; second retreatment is optional if moderate or severe pain recurs (as measured by categorical pain scale or VAS greater than 50 mm), retreat with 8 Gy after > 4 weeks
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
8 Gy in a single fraction; retreatments > 4 weeks, using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy) ; second reirradiation with 8 Gy using local RT fields optional (at discretion of PI);
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
12 Gy in 4 fractions of 3 Gy in 2 consecutive days interfraction interval of a minimum of 6 hrs; retreatments > 4 weeks using local RT fields to sites of residual or recurrent, moderate or severe pain with a single fraction of 8 Gy); second reirradiation with 8 Gy using local RT fields optional (at discretion of PI) ;
Primary Outcome Measure Information:
Title
Pain Relief (response rate) at 4 weeks
Time Frame
Up to 52 weeks
Secondary Outcome Measure Information:
Title
Onset and Duration of Pain Relief in Responders
Time Frame
Up to 52 weeks
Title
Toxicity
Time Frame
Up to 52 weeks
Title
Quality of Life
Time Frame
Up to 52 weeks
Title
Rates of Pathological Fractures and Spinal Cord Compression
Time Frame
Up to 52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: histological diagnosis of malignancy associated with radiological evidence of painful bone metastasis If patients with two sites of pain requiring separate treatment are to be entered, the same randomized treatment option will be used for both sites, but response at each site will be scored and analyzed separately. age > 18 years anticipated remaining life of at least 12 weeks (3 months) informed consent Exclusion Criteria: Primary histology myeloma Sites of previous RT or previous radioisotope treatment conditions or circumstances, which may interfere with treatment or follow-up complicated bone metastasis (pathological fractures, metastatic spinal cord compression)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elena Fidarova, MD
Organizational Affiliation
International Atomic Energy Agency
Official's Role
Study Chair
Facility Information:
Facility Name
Centre Pierre et Marie Curie, Centre hospitalier universitaire Mustapha (CHU)
City
Alger
ZIP/Postal Code
16016
Country
Algeria
Facility Name
Irmandade de Santa Casa de Misericordia de Porto Alegre
City
Porto Alegre
ZIP/Postal Code
90020-090
Country
Brazil
Facility Name
Misr Oncology Center (MOC)
City
Cairo
Country
Egypt
Facility Name
Tata Memorial Hospital
City
Mumbai
ZIP/Postal Code
Maharashtra 400 012
Country
India
Facility Name
Institute of Oncology, University of Vilinius
City
Vilnius
ZIP/Postal Code
08660
Country
Lithuania
Facility Name
Institute of Radiotherapy and Oncology
City
Skopje
ZIP/Postal Code
1000
Country
Macedonia, The Former Yugoslav Republic of
Facility Name
Instituto Nacional de Cancerología (INCAN)
City
Ciudad de Mexico
ZIP/Postal Code
14080
Country
Mexico
Facility Name
Institute of Oncology and Radiology
City
Belgrade
ZIP/Postal Code
11000
Country
Serbia
Facility Name
Hospital Clinic Universidad de Barcelona
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
Facility Name
Hospital Son Dureta
City
Palma de Mallorca
ZIP/Postal Code
07014
Country
Spain
Facility Name
Institut national de cancer Salah Azaiz
City
Tunis
ZIP/Postal Code
Bab Saadoun 1006
Country
Tunisia
Facility Name
Mount Vernon Cancer Centre
City
Northwood
ZIP/Postal Code
HA6 2 RN
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
8823258
Citation
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Results Reference
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PubMed Identifier
11395246
Citation
Salazar OM, Sandhu T, da Motta NW, Escutia MA, Lanzos-Gonzales E, Mouelle-Sone A, Moscol A, Zaharia M, Zaman S. Fractionated half-body irradiation (HBI) for the rapid palliation of widespread, symptomatic, metastatic bone disease: a randomized Phase III trial of the International Atomic Energy Agency (IAEA). Int J Radiat Oncol Biol Phys. 2001 Jul 1;50(3):765-75. doi: 10.1016/s0360-3016(01)01495-x.
Results Reference
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PubMed Identifier
7521863
Citation
Mithal NP, Needham PR, Hoskin PJ. Retreatment with radiotherapy for painful bone metastases. Int J Radiat Oncol Biol Phys. 1994 Jul 30;29(5):1011-4. doi: 10.1016/0360-3016(94)90396-4.
Results Reference
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PubMed Identifier
1372126
Citation
Hoskin PJ, Price P, Easton D, Regan J, Austin D, Palmer S, Yarnold JR. A prospective randomised trial of 4 Gy or 8 Gy single doses in the treatment of metastatic bone pain. Radiother Oncol. 1992 Feb;23(2):74-8. doi: 10.1016/0167-8140(92)90338-u.
Results Reference
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PubMed Identifier
12573746
Citation
Wu JS, Wong R, Johnston M, Bezjak A, Whelan T; Cancer Care Ontario Practice Guidelines Initiative Supportive Care Group. Meta-analysis of dose-fractionation radiotherapy trials for the palliation of painful bone metastases. Int J Radiat Oncol Biol Phys. 2003 Mar 1;55(3):594-605. doi: 10.1016/s0360-3016(02)04147-0.
Results Reference
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PubMed Identifier
9423999
Citation
Gaze MN, Kelly CG, Kerr GR, Cull A, Cowie VJ, Gregor A, Howard GC, Rodger A. Pain relief and quality of life following radiotherapy for bone metastases: a randomised trial of two fractionation schedules. Radiother Oncol. 1997 Nov;45(2):109-16. doi: 10.1016/s0167-8140(97)00101-1.
Results Reference
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PubMed Identifier
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Citation
Arcangeli G, Micheli A, Arcangeli G, Giannarelli D, La Pasta O, Tollis A, Vitullo A, Ghera S, Benassi M. The responsiveness of bone metastases to radiotherapy: the effect of site, histology and radiation dose on pain relief. Radiother Oncol. 1989 Feb;14(2):95-101. doi: 10.1016/0167-8140(89)90053-4.
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Optimization of Radiotherapy in Treatment of Painful Bone Metastasis

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