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A Global, Observational Open Cohort Study to Understand Evolving Treatment Patterns and Real-World Outcomes in Patients with Early-Stage (Stage I-III) Non-Small Cell Lung Cancer (NSCLC)

A Global, Observational Open Cohort Study to Understand Evolving Treatment Patterns and Real-World Outcomes in Patients with Early-Stage (Stage I-III) Non-Small Cell Lung Cancer (NSCLC)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1030250814
Enrollment
375
Registered
2026-03-16
Start date
2026-03-16
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

non-small cell lung cancer

Interventions

None listed

Sponsors

Kitagawa Hiroshi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Stage I-III (AJCC v8 or v9) at initial NSCLC diagnosis -Aged 18 years or older at first diagnosis of NSCLC (20+ years of age in Taiwan)

Exclusion criteria

Exclusion criteria: -Stage III NSCLC patients not amenable to curative intent treatment -NSCLC is not the primary cancer diagnosis -Participation in any interventional clinical trial for initial treatment of Stage I-III NSCLC -History of another primary malignancy except for malignancy treated with curative intent with no known active disease more than 2 years before the diagnosis of NSCLC. Exceptions include adequately resected non-melanoma skin cancer and curatively treated in situ disease. Patients who have received RT with overlapping fields (e.g., cured breast cancer) should be excluded -Any presence of small cell and mixed small-cell and non-small cell histology -A positive pregnancy status at the time of diagnosis

Design outcomes

Primary

MeasureTime frame
-Treatment patterns -Duration of treatment -Time from diagnosis to treatment initiation -Time to treatment discontinuation -Reasons for treatment discontinuation

Secondary

MeasureTime frame
-Subsequent treatment patterns -Adverse events -Biomarker testing -Real-world overall survival (OS) -Real-world progression free survival (rwPFS) -Real-world event free survival (rwEFS) -Real-world disease free survival (rwDFS) -Real-world time to distant metastasis (TTDM)

Countries

Brazil, Canada, Greece, Israel, Japan, KSA, Kuwait, Qatar, Singapore, Switzerland, UAE, United States

Contacts

Public ContactYuko Hayashi

AstraZeneca K.K.

yuko.hayashi1@astrazeneca.com+81-6-4802-3600

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026