During the immune checkpoint inhibitor therapy (ICIT), most of the patients stay at home, but there is lacking of the studies to explore their physical and psychological distress, financial toxicity, care needs, and quality of life. Therefore, the aims of this program are to (1) explore the immune-related adverse event (irAE) severity, distress, financial toxicity, and quality of life and examine the psychometric testing of the Functional Assessment of Cancer Therapy-Immune Checkpoint Modulator (FACT-ICM); (2) establish the LINE group for assessing irAE severity and change trajectory of quality of life in one-year follow-up and (3) combined retrospective chart review and the finding in aim (2) to develop the risk prediction model in order to identify the high risk population.
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Patient-Report Outcome-- Common Terminology Criteria for adverse events (PRO-CTCAE)
Timeframe: The data will be collected once a week within 3 months and once in 3-4 weeks in 4th-12th months during treatment.
Symptom Severity Scale (SSS)
Timeframe: The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
Distress Thermometer (DT)
Timeframe: The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
The COmprehensive Score for financial Toxicity-Functional Assessment of Chronic Illness Therapy (COST-FACIT)
Timeframe: The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
The Functional Assessment of Cancer Therapy-Immune Checkpoint Modulator (FACT-ICM)
Timeframe: The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire 30 (EORTC-QLQ-C30)
Timeframe: The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)
Supportive Care Needs Survey-Short Form 34 (SCNS-SF34)
Timeframe: The data will be collected at five times (Before treatment for baseline, the 3rd, 6th, 9th, and 12th month)