Radiation During Osimertinib Treatment: a Safety and Efficacy Cohort Study

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

January 20, 2022

Primary Completion Date

March 31, 2026

Study Completion Date

December 31, 2026

Conditions
NSCLCEGFR Positive Non-small Cell Lung CancerOligoprogression
Interventions
DRUG

Osimertinib

Osimertinib: according to its marketing authorization, i.e. at daily doses of 80 mg, for a maximum of 12 months within the study.

RADIATION

Radiotherapy

"Radiotherapy: according to standard of care~The target population will comprise 3 parallel cohorts, for cohort 1 and 3 a minimum of 10 subjects is planned to be enrolled:~1. Irradiation of bone, solid organ (non-lung, non-brain) or soft-tissue metastases~2. Irradiation of brain metastases (initial lesion size \< 3 cm)~3. Irradiation of lung lesions (primary tumor or metastases, lesion size \< 5 cm)"

Trial Locations (1)

80336

LMU Klinikum der Universität München, München

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

AstraZeneca

INDUSTRY

lead

AIO-Studien-gGmbH

OTHER