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A confirmatory study of activity of immune checkpoint inhibitors for non-small cell lung cancer patients with interstitial pneumonia

Not Applicable
Conditions
on-small cell lung cancer patients with interstitial pneumonia
Registration Number
JPRN-UMIN000030699
Lead Sponsor
Kitasato University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
1
Inclusion Criteria

Not provided

Exclusion Criteria

1) Systemic administration of steroids at 10 mg/day or more in terms of predonin 2) Active infection requiring systemic treatment 3) Fever of 38 degrees or more at axillary temperature at registration 4) Mental illness or psychiatric symptoms 5) Symptomatic brain metastases 6) Poor control hypertension 7) Continuous systemic administration of immunosuppressants 8) Poor control diabetes 9) Hypersensitivity to the drug 10) Pregnant women, lactating women, women who may be pregnant, or they are not willing to contraceptive 11) In addition, cases judged inappropriate by the attending physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Exacerbation rate of interstitial lung diseases up to 6 months after initiation of immune checkpoint inhibitors
Secondary Outcome Measures
NameTimeMethod
Overall response rate, Progression free survival, Overall survival, Adverse events, Risk factors developing exacerbation of interstial lung disease
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