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      CMET-48. CE7 CANADIAN CLINICAL TRIALS GROUP / ALLIANCE FOR CLINICAL TRIALS IN ONCOLOGY. A PHASE III TRIAL OF STEREOTACTIC RADIOSURGERY COMPARED WITH WHOLE BRAIN RADIOTHERAPY (WBRT) FOR 5–15 BRAIN METASTASES

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          Abstract

          BACKGROUND

          It is now accepted that for patients with 1–4 brain metastases radiosurgery (SRS) provides improved cognitive and quality of life (QoL) outcomes vs. whole-brain radiotherapy (WBRT). It has been our recent finding that SRS also provides overall survival equivalent to WBRT following resection of a brain metastasis, again with improved cognitive and QoL outcomes. A gap in high-level evidence remains for patients with 5 or more brain metastases. We report on the framework of a Phase III trial.

          METHODS

          The NCI Brain Malignancies Steering Committee approved the trial concept in March 2017. The trial is to be led by the NCIC and endorsed by the NRG and Alliance for Clinical Trials in Oncology. Planned total accrual is 206 patients randomized to either radiosurgery (volume-based dosing) or WBRT (30Gy in 10 daily fractions) and memantine. Eligible patients will have a maximum total tumor volume of 30cm 3. They will have 5–15 parenchymal metastases, free of gross leptomeningeal disease and ECOG performance status 0–2. The primary endpoints will be cognitive deterioration free survival and overall survival. Secondary endpoints include those related to: patient/treatment related outcomes (patterns of failure, validation of a nomogram to predict early appearance of new brain metastases, time to (re-)initiation of systemic therapy, etc.), economic endpoints (comparison based on payer rates (Medicare for US / provincial heath authorities in Canadian jurisdictions with activity-based funding) as well as comparison based on “time based activity costing” in selected institutions), dosimetric endpoints, imaging endpoints and quality of life endpoints. Translational endpoints will include analysis of serum samples to elucidate molecular/genomic mechanisms of neurocognitive decline. Additional translational endpoints are contingent on the outcome of applications for supplemental funding.

          CONCLUSIONS

          A collaborative effort has been agreed upon to fill the largest evidence gaps in the focal management of brain metastases.

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          Author and article information

          Journal
          Neuro Oncol
          Neuro-oncology
          neuonc
          Neuro-Oncology
          Oxford University Press (US )
          1522-8517
          1523-5866
          November 2017
          06 November 2017
          : 19
          : Suppl 6 , Abstracts from the 22nd Annual Scientific Meeting and Education Day of the Society for Neuro-Oncology November 16 – 19, 2017, San Francisco, California Including Abstracts from the Society for Neuro-Oncology (SNO) and the Society for CNS Interstitial Delivery of Therapeutics (SCIDOT) Joint Conference on Therapeutic Delivery to the CNS November 15-16, 2017, San Francisco, California
          : vi49
          Affiliations
          [1 ] University of Montreal-CHUM , Montreal, QC, Canada
          [2 ] Mayo Clinic , Rochester, MN, USA
          [3 ] Princess Margaret Hospital , Toronto, ON, Canada
          [4 ] Queen’s University , Kingston, ON, Canada
          [5 ] McMaster University , Hamilton, ON, Canada
          [6 ] Wake Forest Baptist Medical Center , Winston-Salem, NC, USA
          Article
          PMC5692007 PMC5692007 5692007 nox168.194
          10.1093/neuonc/nox168.194
          5692007
          af74cf7f-9ebf-49d8-910a-762228d09a96
          © The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
          History
          Page count
          Pages: 1
          Categories
          Abstracts
          CNS Metastasis

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