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Clinical Trial Summary

This is a prospective Phase II study.The purpose of this study is to monitor the side effects and treatment outcomes of delivering higher doses of radiation therapy to the tumour, while limiting the dose of radiation to the normal tissues. This will be done using a 5 day treatment schedule. The characteristics of patients whose disease remains confined to limited areas in the long term, compared with those who do not will also be described.


Clinical Trial Description

Endpoints are to describe: the proportion of patients with local control for the index site at 1 year; the number of index lesion(s) with local control at 1 year; acute and late AEs related to SBRT; time to local progression for the index site; time to distant disease progression; symptom and QoL profile; median survival. ;


Study Design


Related Conditions & MeSH terms

  • Solid Tumors With Oligometastatic Spread

NCT number NCT01761929
Study type Interventional
Source University Health Network, Toronto
Contact
Status Completed
Phase Phase 2
Start date March 7, 2013
Completion date February 8, 2023