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Stereotactic Radiosurgery for Soft Tissue Sarcoma

Primary Purpose

Soft Tissue Sarcoma

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
CyberKnife
Sponsored by
The Cooper Health System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Soft Tissue Sarcoma

Eligibility Criteria

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

Inclusion Criteria:

  • All cohorts:
  • Age > 18
  • Patients of child-bearing age must agree to contraception until radiosurgery has been completed.
  • Note that patients with metastatic disease are eligible for protocol
  • Cohort 1: Soft tissue sarcoma (of any histology subtype) in patients that are -planned to have pre-operative radiation followed by surgical resection
  • Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip)
  • Patient performance status and co-morbid conditions to allow for surgical resection
  • Cohort 2: soft tissue sarcoma (of any histologic subtype) post-resection with no further plans for additional surgery.
  • Patients must have high risk feature requiring post-operative radiation which can include Large tumor (> 5 cm), High grade, Previous unplanned, non, oncologic surgery, Close margins
  • Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip)
  • Cohort 3: soft tissue sarcoma (of any histologic subtype) that is not amenable to surgical resection for any reason
  • Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip and pelvis)
  • Patients cannot have planned surgical resection
  • Note that retroperitoneal sarcomas are not eligible

Exclusion Criteria:

-Tumors that do not fit criteria for any of the above cohorts

Sites / Locations

  • MD Anderson Cancer Center at CooperRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

A: pre-operative

B: Post-operative

C: Non-resectable

Arm Description

Radiation- CyberKnife: 35-40 Gy over 5 fractions Surgery: Surgical resection of sarcoma

Radiation- CyberKnife: 40 Gy over 5 fractions

Radiation- CyberKnife: 50 Gy over 5 fractions

Outcomes

Primary Outcome Measures

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Progression Free Survival

Secondary Outcome Measures

quality of life
change in tumor burden by RECIST 1.1 response assessment
overall survival

Full Information

First Posted
October 2, 2015
Last Updated
March 7, 2016
Sponsor
The Cooper Health System
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1. Study Identification

Unique Protocol Identification Number
NCT02706171
Brief Title
Stereotactic Radiosurgery for Soft Tissue Sarcoma
Official Title
Stereotactic Radiosurgery for Soft Tissue Sarcoma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
June 2015 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Cooper Health System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is evaluating treatment with CyberKnife for soft tissue sarcomas.
Detailed Description
Because of these possible advantages of SBRT over conventional radiation, the investigators began a small pilot study to test this new treatment technique in the setting of resectable soft tissue sarcomas. The pilot study was planned for a total of 12 patients which was felt to be a good number to gauge if further expansion of this technology would be successful. As of 2/6/2015 13 participants have enrolled (two enrolled patients declined treatment on protocol and thus a total of 11 patients have been treated on protocol). As of this time, the investigators have not had seen Grade 3 or higher toxicity and no instance of local failure. There have been several distant failures which would not be related to local therapy like SBRT and if anything, SBRT should reduce instance of distant failure by shortening time to chemotherapy. The following represents the initial experience for SBRT for STS (from manuscript submitted for publication). Note that on the below abstract 8 participants were treated on the pilot study while 5 participants were treated prior to pilot study opening (the one instance of local failure is from patient treated pre-protocol). In terms of patient numbers the goal is to have 33 patients in cohorts one and two. Using historical controls of late toxicity rates of 40% and late toxicity rates in the initial population of 20% with an alpha of 0.1 (which is reasonable for phase II studies, an alpha of 0.05 is typical for phase III studies) there would be 80% power to detect a difference with 33 patients. The expectation for this phase II study includes the following Late toxicity 30% or less Local control rates 90% or better These numbers are based on historical controls and previous research. Local control rates for historical series have been 90% or better and this also held true in the initial phase II study. For late toxicity rates, historical controls are 35-43% (The NCI study that used similar wound complication definitions to us and was a well powered study had a wound complication rate of 43%). The investigators feel that for this study to be promising enough for large phase III non-inferiority studies that the current phase II study should have late toxicity rates of 30% or better and local control rates of 90% or better.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Soft Tissue Sarcoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A: pre-operative
Arm Type
Experimental
Arm Description
Radiation- CyberKnife: 35-40 Gy over 5 fractions Surgery: Surgical resection of sarcoma
Arm Title
B: Post-operative
Arm Type
Experimental
Arm Description
Radiation- CyberKnife: 40 Gy over 5 fractions
Arm Title
C: Non-resectable
Arm Type
Experimental
Arm Description
Radiation- CyberKnife: 50 Gy over 5 fractions
Intervention Type
Radiation
Intervention Name(s)
CyberKnife
Other Intervention Name(s)
CK
Primary Outcome Measure Information:
Title
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time Frame
1-2 months
Title
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time Frame
1 year
Title
Progression Free Survival
Time Frame
5 years
Secondary Outcome Measure Information:
Title
quality of life
Time Frame
2 months, 4 months, 6 months
Title
change in tumor burden by RECIST 1.1 response assessment
Time Frame
1-2 months, 4 months
Title
overall survival
Time Frame
6 months, 1 year, 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All cohorts: Age > 18 Patients of child-bearing age must agree to contraception until radiosurgery has been completed. Note that patients with metastatic disease are eligible for protocol Cohort 1: Soft tissue sarcoma (of any histology subtype) in patients that are -planned to have pre-operative radiation followed by surgical resection Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip) Patient performance status and co-morbid conditions to allow for surgical resection Cohort 2: soft tissue sarcoma (of any histologic subtype) post-resection with no further plans for additional surgery. Patients must have high risk feature requiring post-operative radiation which can include Large tumor (> 5 cm), High grade, Previous unplanned, non, oncologic surgery, Close margins Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip) Cohort 3: soft tissue sarcoma (of any histologic subtype) that is not amenable to surgical resection for any reason Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip and pelvis) Patients cannot have planned surgical resection Note that retroperitoneal sarcomas are not eligible Exclusion Criteria: -Tumors that do not fit criteria for any of the above cohorts
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kimberly Krieger
Phone
856-735-6237
Facility Information:
Facility Name
MD Anderson Cancer Center at Cooper
City
Camden
State/Province
New Jersey
ZIP/Postal Code
08103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kim Krieger
Phone
856-735-6237

12. IPD Sharing Statement

Citations:
PubMed Identifier
35387414
Citation
Kubicek GJ, Kim TW, Gutowski CJ, Kaden M, Eastwick G, Khrizman P, Xu Q, Lackman R. Preoperative Stereotactic Body Radiation Therapy for Soft-Tissue Sarcoma: Results of Phase 2 Study. Adv Radiat Oncol. 2021 Nov 20;7(2):100855. doi: 10.1016/j.adro.2021.100855. eCollection 2022 Mar-Apr.
Results Reference
derived

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Stereotactic Radiosurgery for Soft Tissue Sarcoma

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