SCION: SABR and Checkpoint Inhibition of NSCLC

PHASE2WithdrawnINTERVENTIONAL
0
Timeline

Start Date

August 11, 2023

Primary Completion Date

December 31, 2026

Study Completion Date

June 30, 2027

Conditions
Non Small Cell Lung CancerCarcinoma, Non-Small-Cell LungNon-small Cell Lung Cancer Stage ILung CancerLung Cancer Stage ILung Adenocarcinoma, Stage ILung Squamous Cell Carcinoma Stage I
Interventions
DRUG

Durvalumab

Subjects will receive durvalumab 1500mg IV every four weeks for four cycles, undergo assessment for residual disease, then a subset of subjects will receive an additional eight cycles of durvalumab.

RADIATION

Stereotactic Body Radiotherapy

Subjects will receive stereotactic radiation therapy concurrent with cycle 2 of durvalumab to a dose of 48Gy in four fractions. Fractionation may be modified for central tumors.

DIAGNOSTIC_TEST

Circulating Tumor DNA assay

After four cycles of durvalumab, subjects will be evaluated at the MRD Landmark for residual ctDNA to determine subsequent treatment assignment.

Trial Locations (5)

V1Y 5L3

BC Cancer--Kelowna, Kelowna

V3V 1Z2

BC Cancer--Surrey, Surrey

V5Z 4E6

BC Cancer--Vancouver, Vancouver

V8R 6V5

BC Cancer--Victoria, Victoria

L8V 5C2

Juravinski Cancer Centre, Hamilton

Sponsors
All Listed Sponsors
collaborator

AstraZeneca

INDUSTRY

collaborator

Ozmosis Research Inc.

INDUSTRY

lead

University of British Columbia

OTHER