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Single Dose Radiotherapy (SDRT) in Oligometatstasis Ablation (OLIGO)

Primary Purpose

Metastatic Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Single Dose Radiotherapy (SDRT)
Sponsored by
Fundacao Champalimaud
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Histologic confirmation of malignancy;
  • FDG PET/CT (or other tracer) PET/CT evidence of limited (1-5) metastases;
  • All detectable lesions must be considered amenable to SDRT or hypofractionated ablation;
  • Age ≥ 18 years;
  • Life expectancy > 6 months;
  • EGOG Performance Status 0-2;
  • Signed informed consent form for treatment;

Exclusion Criteria:

  • Overt poly-metastatic disease (≥5 lesions) as shown by PET/CT scanning;
  • Performance status >2;
  • Severe, active co-morbidity;
  • Significant psychiatric illness;

Sites / Locations

  • Champalimaud Centre for the UnknownRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Single Dose Radiotherapy (SDRT)

Arm Description

Single Dose Radiotherapy (SDRT) at a prescription dose of 24 Gy to all detectable metastatic lesions

Outcomes

Primary Outcome Measures

Efficacy of SDRT ablation
Efficacy of Single Dose Radiotherapy (SDRT 24Gy) of metastatic lesions measured by PERCIST criteria with repeated PET-CT studies.

Secondary Outcome Measures

Progression-free survival
Local failure and poly-metastasis-free survival following metastasis-directed ablation in limited volume oligometastatic disease will be determined by sequential PET/CT evaluations

Full Information

First Posted
February 16, 2018
Last Updated
July 22, 2019
Sponsor
Fundacao Champalimaud
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1. Study Identification

Unique Protocol Identification Number
NCT03543696
Brief Title
Single Dose Radiotherapy (SDRT) in Oligometatstasis Ablation
Acronym
OLIGO
Official Title
Phase II Clinical Study to Ablate Oligometastatic Deposits by Single Dose Radiotherapy (SDRT) and Metabolic Assessment of Outcome
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2011 (Actual)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundacao Champalimaud

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study focuses on treatment outcomes of human metastatic cancer which usually fares with dismal (<5%) survival at 5 years following first diagnosis of a metastasis. However, a subgroup of patients with an initial oligometastatic presentation (i.e. 1-5 clinically detectable lesions) have been reported to respond to complete surgical removal of detectable deposits with up to 20% disease-free survival at 10 years. Patients relapsing with a second oligometastatic presentation respond to a second round of ablation with encouraging rates of 5-year disease free survival. Based on patterns of response to therapy and relapse, we propose investigate on the hypothesis that metastatic disease may be limited in extent, slowly growing and amenable to successive eradication of metastatic deposits. For visible tumor ablation, we propose to employ the effective and safe technique of Single Dose Image-Guided Radiotherapy (SDRT) and to optimize its use in conjunction with systemic therapy. Where SDRT at a full ablative dose (24Gy) is deemed unfeasible, hypofractionated SBRT (9Gy x3) will be offered. Response assessment will be via local control, poly-metastasis-free survival and overall survival rates. Preliminary phase I/II studies indicate remarkable benefits from the SDRT/SBRT in patients with limited metastatic disease. The expected outcomes may be significant conceptual and practical changes in the management of selected metastatic settings resulting in long-term periods of disease-free and overall survival in settings presently associated with dismal prognosis.
Detailed Description
This phase II clinical trial is designed assess clinical outcomes following ablation by Single Dose Image Guided Radiotherapy (SDRT) in patients with oligometastatic (OM) presentation (1-5 clinically detectable lesions). For local tumor ablation the investigators will use the novel non-invasive and highly effective technique of SDRT which is capable of conferring long-term local relapse-free rates in approximately 90% of metastatic lesions independently of tumour histology. Historical series with various tumor histologies have shown subgroups of patients with an initial oligometastatic presentation respond to complete surgical removal of detectable deposits, yielding up to 20% disease-free survival at 10 years. The study will determine response rates by metabolic criteria (i.e. PERCIST). Pre- and post-treatment assessment are performed by FDG (or other appropriate PET tracer) PET/CT scans with acquisition of information on lesion(s) location, volume and metabolic parameters. Changes in metabolic avidity post treatment can be used to evaluate the rates of complete metabolic response, stable disease and progression at the site(s) of SDRT to measure local relapse-free survival intervals (LRFS and the kinetics of tracer uptake may serve as a potential predictive tool of treatment response). Additionally, whole-body PET/CT scans can be used to assess distant metastasis-free progression, polymetatstasis-free survival (PMFS). Lesions which are not amenable to the SDRT approach due to the inability to safely fulfill dose/volume constraints, are consistently treated with a hypofractionated approach of three sessions of 9Gy, an established and safe treatment regimen. Comparisons in LRFS, persistence of the oligometastatic status, distant metastasis free-survival, poly-metastasis-free survival, interval between repeat treatments and overall survival will be evaluated evaluated. The impact of systemic treatment, as per current established clinical practices, will also be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Single Dose Radiotherapy (SDRT)
Arm Type
Experimental
Arm Description
Single Dose Radiotherapy (SDRT) at a prescription dose of 24 Gy to all detectable metastatic lesions
Intervention Type
Radiation
Intervention Name(s)
Single Dose Radiotherapy (SDRT)
Primary Outcome Measure Information:
Title
Efficacy of SDRT ablation
Description
Efficacy of Single Dose Radiotherapy (SDRT 24Gy) of metastatic lesions measured by PERCIST criteria with repeated PET-CT studies.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Progression-free survival
Description
Local failure and poly-metastasis-free survival following metastasis-directed ablation in limited volume oligometastatic disease will be determined by sequential PET/CT evaluations
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic confirmation of malignancy; FDG PET/CT (or other tracer) PET/CT evidence of limited (1-5) metastases; All detectable lesions must be considered amenable to SDRT or hypofractionated ablation; Age ≥ 18 years; Life expectancy > 6 months; EGOG Performance Status 0-2; Signed informed consent form for treatment; Exclusion Criteria: Overt poly-metastatic disease (≥5 lesions) as shown by PET/CT scanning; Performance status >2; Severe, active co-morbidity; Significant psychiatric illness;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carlo Greco, MD
Email
carlo.greco@fundacaochampalimaud.pt
First Name & Middle Initial & Last Name or Official Title & Degree
Manuela Seixas
Email
manuela.seixas@fundacaochampalimaud.pt
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlo Greco, MD
Organizational Affiliation
Fundacao Champalimaud
Official's Role
Principal Investigator
Facility Information:
Facility Name
Champalimaud Centre for the Unknown
City
Lisbon
ZIP/Postal Code
1800
Country
Portugal
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlo Greco
Email
carlo.greco@fundacaochampalimaud.pt

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32777335
Citation
Greco C, Kolesnick R, Fuks Z. Conformal Avoidance of Normal Organs at Risk by Perfusion-Modulated Dose Sculpting in Tumor Single-Dose Radiation Therapy. Int J Radiat Oncol Biol Phys. 2021 Jan 1;109(1):288-297. doi: 10.1016/j.ijrobp.2020.08.017. Epub 2020 Aug 7.
Results Reference
derived

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Single Dose Radiotherapy (SDRT) in Oligometatstasis Ablation

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