search
Back to results

Radiofrequency Ablation in Treating Patients With Bone Metastases (ACRIN-6661)

Primary Purpose

Metastatic Cancer, Pain, Unspecified Adult Solid Tumor, Protocol Specific

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
pain therapy
radiofrequency ablation
Sponsored by
American College of Radiology Imaging Network
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Cancer focused on measuring bone metastases, pain, unspecified adult solid tumor, protocol specific

Eligibility Criteria

21 Years - 120 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

4.1 Inclusion Criteria 4.1.1 Histologically or cytologically documented malignant disease with a bone lesion that has the clinical and/imaging features of metastatic disease. 4.1.2 Persistent intractable pain that results in a return visit to the oncologist. The measurable pain must be above a pain scale of five (scale of 0-10). (Pain during the last week described as "the worst" by the patient on a scale of 0 (no pain) to 10 (pain as bad as patient can imagine)). 4.1.3 The patient's pain must be from a solitary site of metastatic disease in the bone. Each site must be amenable to RFA utilizing a percutaneous CT-guided approach. (RF electrode can be safely placed under CT guidance without harm to normal structures.) 4.1.4 The maximum size of the bone metastasis (study site) must be no greater than 8 cm. 4.1.5 Radiofrequency treatment can be performed within 5 days of baseline evaluations. 4.1.6 All patients must understand and sign a study-specific informed consent. 4.2 Exclusion Criteria 4.2.1 Tumor mass in contact with hollow viscera. 4.2.2 Uncontrolled coagulopathy or bleeding diathesis that cannot be corrected with FFP and platelets prior to procedure. (Platelets must be ≥ 70,000/ul.) 4.2.3 Aspirin and nonsteroidal anti-inflammatory medications, antiplatelet medications, or warfarin must be discontinued prior to the procedure for a time period that is appropriate given the drug half life and the drugs known antiplatelet activity (e.g. aspirin for 7 days and ibuprofen 24 hours). Low molecular weight heparin preparations must be discontinued 24 hours prior to procedure. 4.2.4 Tumor involves a weight-bearing long-bone of the lower extremity. 4.2.5 Site of tumor surgically stabilized with metallic hardware. 4.2.6 Previous (within 30 days immediately prior to RFA or post RFA) or scheduled concurrent systemic treatment of metastases with external beam radiation or radioisotopes. (Chemotherapy will not be allowed within 14 days prior to and within 14 days post RFA procedure). 4.2.7 Patients with primary musculoskeletal malignancies, lymphoma and leukemia will not be RFA treatment candidates. 4.2.8 Spinal metastases that do not have an intact cortex between the mass and the spinal canal and exiting nerve roots. 4.2.8 Patients with a pacemaker.

Sites / Locations

  • Comprehensive Cancer Center at University of Alabama at Birmingham
  • UMASS Memorial Cancer Center - University Campus
  • Mallinckrodt Institute of Radiology at Washington University Medical Center
  • Radiology Consultants, Incorporated
  • Abramson Cancer Center of the University of Pennsylvania
  • Kimmel Cancer Center at Thomas Jefferson University - Philadelphia
  • Comprehensive Cancer Center at Rhode Island Hospital
  • M.D. Anderson Cancer Center at University of Texas

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

RFA as pain therapy

Arm Description

Changes in the severity of pain as measured using using the Memorial Pain Assessment Cards (MPAC) before and after RadioFrequency Ablation (RFA) will be statistically analyzed

Outcomes

Primary Outcome Measures

Adverse events
Estimate the adverse event rate due to RFA within 1 month follow-up period.

Secondary Outcome Measures

Pain intensity
pain intensity as measured by VASPI Scale
Pain intensity
pain intensity as measured by VASPI Scale
Pain reduction
pain reduction as measured by VASPR Scale
Pain reduction
pain reduction as measured by VASPR Scale
Mood
Mood as measured byt the VASMOOD scale
Mood
Mood as measured by the VASMOOD scale
Pain Severity
Pain severity as measured by the Tursky scale
Pain Severity
Pain severity as measured by the Tursky scale

Full Information

First Posted
November 9, 2001
Last Updated
July 2, 2019
Sponsor
American College of Radiology Imaging Network
Collaborators
National Cancer Institute (NCI)
search

1. Study Identification

Unique Protocol Identification Number
NCT00026247
Brief Title
Radiofrequency Ablation in Treating Patients With Bone Metastases
Acronym
ACRIN-6661
Official Title
A Phase I/II Study of Percutaneous Radiofrequency Ablation of Bone Metastases Using CT Guidance
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
November 2001 (undefined)
Primary Completion Date
February 15, 2010 (Actual)
Study Completion Date
February 15, 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
American College of Radiology Imaging Network
Collaborators
National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Radiofrequency ablation may be effective in decreasing pain from bone metastases. PURPOSE: Phase I/II trial to study the effectiveness of radiofrequency ablation in decreasing pain in patients who have bone metastases.
Detailed Description
OBJECTIVES: Determine the side effects of radiofrequency ablation in patients with bone metastases. Determine the effect of this regimen on pain in these patients. Determine the effect of this regimen on mood in these patients. Determine the effects of narcotic usage in patients treated with this regimen. Determine the relationship between laboratory and imaging features of this treatment and the effects of the treatment in these patients. OUTLINE: This is a multicenter study. Patients undergo percutaneous CT-guided radiofrequency ablation directly to the metastatic lesion over approximately 12 minutes. Pain and mood are assessed at baseline, daily for 14 days after treatment, and at 1 and 3 months after treatment. Patients are followed at 1 week and then at 1 and 3 months. PROJECTED ACCRUAL: Approximately 75 patients will be accrued for this study within 12.5 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Cancer, Pain, Unspecified Adult Solid Tumor, Protocol Specific
Keywords
bone metastases, pain, unspecified adult solid tumor, protocol specific

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The outcomes of the study will be adverse event analysis and pain relief.
Masking
None (Open Label)
Allocation
N/A
Enrollment
66 (Actual)

8. Arms, Groups, and Interventions

Arm Title
RFA as pain therapy
Arm Type
Experimental
Arm Description
Changes in the severity of pain as measured using using the Memorial Pain Assessment Cards (MPAC) before and after RadioFrequency Ablation (RFA) will be statistically analyzed
Intervention Type
Procedure
Intervention Name(s)
pain therapy
Intervention Type
Procedure
Intervention Name(s)
radiofrequency ablation
Other Intervention Name(s)
RFA
Primary Outcome Measure Information:
Title
Adverse events
Description
Estimate the adverse event rate due to RFA within 1 month follow-up period.
Time Frame
1 month post procedure
Secondary Outcome Measure Information:
Title
Pain intensity
Description
pain intensity as measured by VASPI Scale
Time Frame
1 month post-procedure
Title
Pain intensity
Description
pain intensity as measured by VASPI Scale
Time Frame
3 months post-procedure
Title
Pain reduction
Description
pain reduction as measured by VASPR Scale
Time Frame
1 month post-procedure
Title
Pain reduction
Description
pain reduction as measured by VASPR Scale
Time Frame
3 month post-procedure
Title
Mood
Description
Mood as measured byt the VASMOOD scale
Time Frame
1 month post-procedure
Title
Mood
Description
Mood as measured by the VASMOOD scale
Time Frame
3 month post-procedure
Title
Pain Severity
Description
Pain severity as measured by the Tursky scale
Time Frame
1 month post-procedure
Title
Pain Severity
Description
Pain severity as measured by the Tursky scale
Time Frame
3 month post-procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
4.1 Inclusion Criteria 4.1.1 Histologically or cytologically documented malignant disease with a bone lesion that has the clinical and/imaging features of metastatic disease. 4.1.2 Persistent intractable pain that results in a return visit to the oncologist. The measurable pain must be above a pain scale of five (scale of 0-10). (Pain during the last week described as "the worst" by the patient on a scale of 0 (no pain) to 10 (pain as bad as patient can imagine)). 4.1.3 The patient's pain must be from a solitary site of metastatic disease in the bone. Each site must be amenable to RFA utilizing a percutaneous CT-guided approach. (RF electrode can be safely placed under CT guidance without harm to normal structures.) 4.1.4 The maximum size of the bone metastasis (study site) must be no greater than 8 cm. 4.1.5 Radiofrequency treatment can be performed within 5 days of baseline evaluations. 4.1.6 All patients must understand and sign a study-specific informed consent. 4.2 Exclusion Criteria 4.2.1 Tumor mass in contact with hollow viscera. 4.2.2 Uncontrolled coagulopathy or bleeding diathesis that cannot be corrected with FFP and platelets prior to procedure. (Platelets must be ≥ 70,000/ul.) 4.2.3 Aspirin and nonsteroidal anti-inflammatory medications, antiplatelet medications, or warfarin must be discontinued prior to the procedure for a time period that is appropriate given the drug half life and the drugs known antiplatelet activity (e.g. aspirin for 7 days and ibuprofen 24 hours). Low molecular weight heparin preparations must be discontinued 24 hours prior to procedure. 4.2.4 Tumor involves a weight-bearing long-bone of the lower extremity. 4.2.5 Site of tumor surgically stabilized with metallic hardware. 4.2.6 Previous (within 30 days immediately prior to RFA or post RFA) or scheduled concurrent systemic treatment of metastases with external beam radiation or radioisotopes. (Chemotherapy will not be allowed within 14 days prior to and within 14 days post RFA procedure). 4.2.7 Patients with primary musculoskeletal malignancies, lymphoma and leukemia will not be RFA treatment candidates. 4.2.8 Spinal metastases that do not have an intact cortex between the mass and the spinal canal and exiting nerve roots. 4.2.8 Patients with a pacemaker.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Damian E. Dupuy, MD
Organizational Affiliation
Rhode Island Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Comprehensive Cancer Center at University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Facility Name
UMASS Memorial Cancer Center - University Campus
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Facility Name
Mallinckrodt Institute of Radiology at Washington University Medical Center
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
Radiology Consultants, Incorporated
City
Youngstown
State/Province
Ohio
ZIP/Postal Code
44512
Country
United States
Facility Name
Abramson Cancer Center of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4283
Country
United States
Facility Name
Kimmel Cancer Center at Thomas Jefferson University - Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107-5541
Country
United States
Facility Name
Comprehensive Cancer Center at Rhode Island Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Facility Name
M.D. Anderson Cancer Center at University of Texas
City
Houston
State/Province
Texas
ZIP/Postal Code
77030-4009
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All De-identified study data is available to request from ACRIN: https://www.acrin.org/RESEARCHERS/POLICIES/DATAANDIMAGESHARINGPOLICY.aspx
Citations:
PubMed Identifier
20041484
Citation
Dupuy DE, Liu D, Hartfeil D, Hanna L, Blume JD, Ahrar K, Lopez R, Safran H, DiPetrillo T. Percutaneous radiofrequency ablation of painful osseous metastases: a multicenter American College of Radiology Imaging Network trial. Cancer. 2010 Feb 15;116(4):989-97. doi: 10.1002/cncr.24837.
Results Reference
result

Learn more about this trial

Radiofrequency Ablation in Treating Patients With Bone Metastases

We'll reach out to this number within 24 hrs