This study will review medical records of adults with cancer who received nivolumab either as an intravenous (IV) infusion or as a subcutaneous (under the skin) injection in community oncology clinics in the United States. The study will describe who receives each type of treatment, how the treatments are used, and selected safety events such as reactions at the injection or infusion site and infections.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Participant age
Timeframe: Baseline
Participant sex
Timeframe: Baseline
Participant race
Timeframe: Baseline
Participant ethnicity
Timeframe: Baseline
Body mass index (kg/m²)
Timeframe: Baseline
Smoking status
Timeframe: Baseline
Cancer diagnosis
Timeframe: Baseline
Disease stage at initial diagnosis (Stage 0-IV, unknown)
Timeframe: Baseline
Eastern Cooperative Oncology Group (ECOG) performance status distribution (0-4, unknown)
Timeframe: Baseline
Number of participants by tumor histology categories as applicable for each disease type, including unknown.
Timeframe: Baseline
Duration of therapy (days)
Timeframe: Up to 6 months
Duration of planned therapy (days)
Timeframe: Up to 6 months
Dose administered at index (mg)
Timeframe: Baseline
Concomitant anti-cancer therapy use
Timeframe: Baseline
Location of injection site (thigh or abdomen)
Timeframe: Up to 6 months
Number of participants with treatment switches or discontinuation.
Timeframe: Up to 6 months