SBRT for Extra-cranial Oligorecurrent Tumor
Primary Purpose
Recurrent Cancer
Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
SBRT
systemic therapy (chemotherapy, hormon therapy, target therapy etc)
palliative RT
Sponsored by
About this trial
This is an interventional treatment trial for Recurrent Cancer focused on measuring stereotactic body radiotherapy
Eligibility Criteria
Inclusion Criteria:
- age <18 years old
- ECOG score: 0-2
- number of distant metastases: 1-5
- all cancers (except lymphoma, myeloma, and germ cell tumor)
- status of primary lesion: cured
- pathologically confirmed cancer
- life expectancy: over 6 months
Exclusion Criteria:
- recurrent lesion which had been treated by radiotherapy
- complete response after systemic therapy
- patients who cannot be treated with SBRT due to any reason.
- pregnancy or breast-feeding
- malignant pleural effusion
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Arm 1
Arm 2
Arm Description
systemic therapy+palliative RT
systemic therapy+SBRT
Outcomes
Primary Outcome Measures
disease progression free survival rate
Secondary Outcome Measures
overall survival rate
local control rate
Number of participants with radiation induced acute or late toxicity
Acute and late toxicities would be evaluated using the Common Terminology Criteria of Adverse Events (CTCAE) version 4.0 and the Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer (RTOG/EORTC) radiation morbidity criteria, respectively.
Full Information
NCT ID
NCT02410187
First Posted
March 20, 2015
Last Updated
March 2, 2016
Sponsor
Korea Cancer Center Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02410187
Brief Title
SBRT for Extra-cranial Oligorecurrent Tumor
Official Title
Stereotactic Body Radiotherapy for Extra-cranial Oligorecurrent Tumor: Randomized Phase II Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2016 (undefined)
Primary Completion Date
March 2018 (Anticipated)
Study Completion Date
March 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea Cancer Center Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Clinical experience has shown that metastasis can often be limited in number and location, and thus amenable to local treatment. The term oligometastasis describes an intermediate state of cancer spread between localized disease and widespread metastasis. The implication of such an intermediate state is that the disease can be cured by using metastasis-directed therapy. Historically, in some patients with oligometastases in the liver or lungs, surgical resection was often indicated, as abundant evidence suggested it could improve progression-free or overall survival. Recently, several studies have reported promising outcomes of >80% local control with Stereotactic Body Radiotherapy (SBRT) in patients with lung or liver oligometastases. Nonetheless, very few studies have focused on non-liver, non-lung extracranial oligometastatic lesions treated with SBRT, and such studies have limitations of a retrospective nature and small sample sizes.Because allmost studies are based on single-arm studies without appropriate controls, the level of evidence to support SBRT is weak. Randomized trials are therefore necessary to establish the utility of SBRT for oligometastatic disease.
This study is designed as a randomized phase II study. Patients will be randomized between current standard treatment (Arm 1) versus standard treatment +SBRT (Arm 2) to all known disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Cancer
Keywords
stereotactic body radiotherapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm 1
Arm Type
Active Comparator
Arm Description
systemic therapy+palliative RT
Arm Title
Arm 2
Arm Type
Experimental
Arm Description
systemic therapy+SBRT
Intervention Type
Radiation
Intervention Name(s)
SBRT
Other Intervention Name(s)
VMAT (Volumetric Modulated Arc Therapy )
Intervention Description
10 Gy x 3 - 20 Gy x 3 (BED 60Gy-180 Gy) or 8 Gy x 4 - 17 Gy x 4 (BED 58-184 Gy)
Intervention Type
Drug
Intervention Name(s)
systemic therapy (chemotherapy, hormon therapy, target therapy etc)
Other Intervention Name(s)
chemotherapy, hormon therapy, target therapy etc.
Intervention Description
Physicians can choose all the options available chemotherapy, hormon therapy, target therapy etc.
Use of chemotherapy schemes containing potent enhancers of radiation damage (e.g. gemcitabine,adriamycin) are discouraged within the first month after SBRT.
Intervention Type
Radiation
Intervention Name(s)
palliative RT
Other Intervention Name(s)
conventional fractionation RT
Intervention Description
fraction size of RT = < 3 Gy
Primary Outcome Measure Information:
Title
disease progression free survival rate
Time Frame
2 years
Secondary Outcome Measure Information:
Title
overall survival rate
Time Frame
2 years
Title
local control rate
Time Frame
2 years
Title
Number of participants with radiation induced acute or late toxicity
Description
Acute and late toxicities would be evaluated using the Common Terminology Criteria of Adverse Events (CTCAE) version 4.0 and the Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer (RTOG/EORTC) radiation morbidity criteria, respectively.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age <18 years old
ECOG score: 0-2
number of distant metastases: 1-5
all cancers (except lymphoma, myeloma, and germ cell tumor)
status of primary lesion: cured
pathologically confirmed cancer
life expectancy: over 6 months
Exclusion Criteria:
recurrent lesion which had been treated by radiotherapy
complete response after systemic therapy
patients who cannot be treated with SBRT due to any reason.
pregnancy or breast-feeding
malignant pleural effusion
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mi-Sook Kim, M.D. Ph.D.
Phone
+82-2-970-1264
Email
mskim@kirams.re.kr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mi-Sook Kim, M.D. Ph.D.
Organizational Affiliation
mskim@kirams.re.kr
Official's Role
Study Chair
12. IPD Sharing Statement
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SBRT for Extra-cranial Oligorecurrent Tumor
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