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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
Korea Cancer Center Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Recurrent Cancer focused on measuring stereotactic body radiotherapy

Eligibility Criteria

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

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

    First Posted
    March 20, 2015
    Last Updated
    March 2, 2016
    Sponsor
    Korea Cancer Center Hospital
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    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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