Researchers already did trials that showed Sorafenib and Regorafenib worked for patients with hepatocellular carcinoma (most common liver tumor type). In this trial, they want to learn more about the same patient group in which Sorafenib or Regorafenib is given after other drugs. Patients participating in this study will be observed until 12 months after the last patient has been enrolled to collect data on how safe the drugs are and how well they are working when used as second line or beyond treatment.
Study Type
OBSERVATIONAL
Enrollment
3
Prescribed by physician.
Prescribed by physician.
Many Locations
Multiple Locations, Germany
Identification of current treatment patterns by means of individual treatment lines in the systemic HCC therapy with regards to Nexavar and Stivarga, i.e. when both drugs are used in ≥ 2nd-line under current practice conditions
Time frame: Up to 24 months
Overall Survival (OS) from start of Nexavar or Stivarga therapy and from start of first systemic therapy
Time frame: Up to 36 months
Progression free survival (PFS)
Time frame: Up to 36 months
Time to progression (TTP)
Time frame: Up to 36 months
Duration of Nexavar or Stivarga treatment
Time frame: Up to 36 months
Tumor response to treatment
Evaluated by the investigator according to the categories "complete response", "partial response", "stable disease", "progressive disease by clinical judgment", "progressive disease measurement proven", "unknown" and "not applicable", and will be analyzed providing absolute and relative frequencies of the tumor status categories.
Time frame: Up to 36 months
Incidence of treatment-emergent adverse events (TEAE)
Time frame: Up to 36 months
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