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. 2020 Apr 22;9(4):e16296. doi: 10.2196/16296

Table 1.

Time of measurement for each end point and associated measurements.

End point Baseline measurement Day of treatment measurement Follow-up measurement
Real-life application of radioembolization
  • Type of liver cancer

  • Prior hepatic procedures

  • Associated systemic therapy (prior systemic therapy)

  • Intention of treatment

  • Postradioembolization hepatic procedures

  • Postradioembolization systemic chemotherapy

Effectiveness end points N/Aa
  • Treatment date

  • Date of effectiveness event (OSb, PFSc, hepatic PFS, IRd)

Safety end points N/A
  • Severe day of treatment complications (Grade 3-4)e

  • Adverse events (Grade 1-5)e

  • Abnormal laboratory values

Technical considerations end points
  • Patient-related characteristics

  • Prior hepatic procedures

  • Physical characteristics (body surface area, lung shunt study [%], Eastern Cooperative Oncology Group performance status)

  • Treatment planning

  • Treatment administration

  • Procedure-related outcomes

N/A
Patient-reported outcome end points
  • EORTCf QLQ-C30g

  • Additional module for HCCh

N/A
  • EORTC QLQ-C30

  • Additional module for HCC

aN/A: not applicable.

bOS: overall survival.

cPFS: progression-free survival.

dIR: imaging response.

eGrading according to Common Terminology Criteria for Adverse Events version 4.03.

fEORTC: European Organisation for the Research and Treatment of Cancer.

gQLQ-C30: Quality of Life Questionnaire C30.

hHCC: hepatocellular carcinoma.