Study identifier:D4194R00013
ClinicalTrials.gov identifier:NCT03995875
EudraCT identifier:N/A
CTIS identifier:N/A
Real world evidence of long-term safety and efficacy in patients treated with durvalumab after concurrent chemoradiation for unresectable stage III NSCLC.
Carcinoma, Non-Small-Cell Lung
N/A
No
-
All
529
Observational
n/a - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Dec 2024 by AstraZeneca
AstraZeneca
The Japan Lung Cancer Society
This observational study is designed to assess the long term safety of the durvalumab treatment period including subsequent treatment period and demonstrate the efficacy of patients treated with durvalumab following chemoradiation therapy in the real world.
Study design: Prospective multi-center non-interventional cohort study Data Source(s): Medical records of patients who are treated with durvalumab following chemoradiation therapy Study Population: Patients prescribed and treated with durvalumab for unresectable stage III non-small cell lung cancer (NSCLC) at first time following chemoradiation therapy and who provide written informed consent. Exposure(s): durvalumab Outcome(s): Summary of pneumonitis and adverse event special interest (AESI), progression free survaival (PFS), overall survaival (OS), Reasons of discontinuation of durvalumab treatment, Details of subsequent treatments after durvalumab Sample Size Estimations: 500 patients Statistical Analysis: Only descriptive analysis and no formal test
Location
Location
Mishima, Shizuoka, Japan
Location
Yokohama, Kanagawa, Japan
Location
Iwakuni, Yamaguchi, Japan
Location
Wakayama, WAKAYAMA, Japan
Location
Saitama, Saitama, Japan
Location
Chiba, Chiba, Japan
Location
Sakai, Osaka, Japan
Location
Okayama, Okayama, Japan
Arms | Assigned Interventions |
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