Table 3.
Agent | Study Type | No. of Patients | HRQoL Assessment Tool | Scale(s)/Domain(s) | Outcome |
---|---|---|---|---|---|
Sorafenib | Prospective | 36 | FACT-Hep | Physical well-being | Score decrease was detected from baseline to week 1, with a median reduction of −8.3 (range: −60.1 to −17.9; p = 0.0003) |
Sorafenib | Prospective | 54 | SF-36 (Japanese Version) |
All domains | Scores >40 maintained over a 1-year period (n = 13) |
Physical functioning | Baseline scores ≥40 significantly associated with longer overall survival (p = 0.053) | ||||
Social functioning | Baseline scores ≥40 associated with longer treatment duration (p = 0.016) | ||||
Lenvatinib | Phase III Trial | 954 | EORTC QLQ-C30, EORTC QLQ-HCC18 | EORTC QLQ-C30: role functioning, pain, and diarrhea EORTC QLQ-HCC18: nutrition and body image |
Clinically meaningful deterioration observed later in lenvatinib compared to sorafenib |
EORTC QLQ-C30 summary score | No significant difference between lenvatinib and sorafenib (HR = 0.87, 95% CI: 0.75–1.01) | ||||
Regorafenib | Phase III Trial | 573 | FACT-G, HACT-Hep, EQ-5D, EQ-VAS | All scales and domains | No clinically meaningful differences between regorafenib and placebo |
Ramucirumab | Subanalysis | 565 | FACT Hepatobiliary Symptom Index (FHSI)-8, EuroQoL (EQ-5D) | All scales and domains | No significant treatment differences |
FHSI-8 | Subpopulation of patients with baseline AFP ≥400ng/mL had significantly reduced deterioration at the end of treatment compared with placebo (p = 0.038) | ||||
Cabozantinib | Subanalysis | 707 | EQ-5D-5L | Quality-adjusted life years (QALY) | Mean accrued QALYs with cabozantinib was +0.115 vs. placebo (95% CI: 0.032 to 0.198; p = 0.007) |
Nivolumab | Phase I/II Trial | 262 | EQ-5D-3L, EQ-5D-VAS | All scales and domains | Stable patient-reported outcomes despite previous treatment with sorafenib |