Durvalumab Followed by Chemoradiation and Consolidation Durvalumab for Stage III Non-small Cell Lung Cancer

PHASE2TerminatedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

June 18, 2020

Primary Completion Date

June 20, 2023

Study Completion Date

February 5, 2024

Conditions
Lung CancerNon-small Cell Carcinoma
Interventions
DRUG

Induction Durvalumab

Induction durvalumab at 1500 mg intravenously (IV) will be given on Day 1 of a four week cycle for 1 cycle,

DRUG

Chemotherapy

Concurrent chemoradiation will be with platinum-based chemotherapy (cisplatin or carboplatin, with etoposide, taxane, or pemetrexed) selected at the treating physician's discretion. The chemotherapy regimen used should be administered per institutional standards following the prescribing guidelines for each drug

RADIATION

Radiation

Treatment will be delivered using IMRT or 3DCRT using typically 6-10MV photons per institutional standards. 4D simulation and appropriate IGRT are encouraged. Radiation therapy must begin within one week of the first day of chemotherapy (or vice versa). Therapy will be 1.8-2 Gy per day; 5 days per week, excluding holidays per institutional standard as this is a standard of care regimen for this patient population. 54-66 Gy will be delivered.

DRUG

Consolidation durvalumab

Durvalumab at 1500 mg intravenously (IV) will be given on Day 1 of a four week cycle for 12 cycles

Trial Locations (5)

55440

HealthPartners Institute, Minneapolis

60612

Rush University Medical Center, Chicago

67214

Cancer Center of Kansas, Wichita

97213

Providence Portland Medical Center, Portland

07922

Summit Medical Group, P. A., Berkeley Heights

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

AstraZeneca

INDUSTRY

collaborator

Providence Cancer Center, Earle A. Chiles Research Institute

OTHER

lead

Rachel Sanborn

OTHER