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A multi-institutional retrospective study of the efficacy and safety of immune checkpoint blockade for patients with non-small cell lung cancer and pre-existing autoimmune disease (NEJ047)

Not Applicable
Completed
Conditions
Patients with non-small cell lung cancer and pre-existing autoimmune disease
Registration Number
JPRN-UMIN000040512
Lead Sponsor
orth East Japan Study Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

None

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Ratio of acute exacerbation of AID in patients with NSCLC and AID who received ICB 2. Rate of serious immune related adverse events (irAE) in patients with NSCLC and AID who received ICB
Secondary Outcome Measures
NameTimeMethod
1. Objective response rate (ORR) 2. Progression-free survival (PFS) 3. Overall survival (OS) 4. Time to treatment failure (TTF)
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