The purpose of this observational study is to describe the patient, disease and treatment characteristics of eligible participants with upper gastrointestinal cancer treated with adjuvant nivolumab.
Study Type
OBSERVATIONAL
Enrollment
250
As per product label
Bayshore Specialty Rx Ltd.
Mississauga, Ontario, Canada
Participant sociodemographics
Time frame: Baseline
Participant Eastern Cooperative Oncology Group (ECOG) score
Time frame: Baseline
Participant histology results
Time frame: Baseline
Participant comorbidities
Time frame: Baseline
Participant tumour location
Time frame: Baseline
Date of tumour resection
Time frame: Baseline
Participant primary upper gastrointestinal cancer diagnosis
Time frame: Baseline
Initial nivolumab dosage prescribed to participants
Time frame: Index date
Number of nivolumab treatments received
Time frame: Up to 484 days
Nivolumab dosage modification
Time frame: Up to 484 days
Nivolumab treatment duration
Time frame: Up to 484 days
Reason for participant discharge
Time frame: Up to 484 days
Participant adverse events (AEs)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: Up to 484 days
Management of participant adverse events (AEs)
Time frame: Up to 484 days