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RECRUITING
NCT07148245

Symptoms of Immune Checkpoint Inhibitor Therapy in Cutaneous Melanoma

Sponsor: University of California, San Francisco

View on ClinicalTrials.gov

Summary

The introduction of immune checkpoint inhibitors (ICIs) for the treatment of patients with stages IIB to IV cutaneous melanoma resulted in dramatic improvements in mortality rates for this common form of cancer. With this rapid shift in treatment, significant gaps in knowledge exist regarding the impact of ICIs on patients' symptom experiences. An in-depth characterization of inter-individual differences in patients' symptom experiences will fill this knowledge gap and assist with the early detection of ICI toxicity; guide symptom management; inform treatment decision making; and refine ICI-symptom instrument development. Furthermore, given the limited knowledge in this area, the identification of demographic, clinical, environmental, and molecular risk factors associated with a worse symptom experience is warranted. This is a longitudinal, prospective study evaluating the symptoms that immune checkpoint inhibitors may cause in patients with cutaneous melanoma.

Official title: Characterization of the Symptom Experience of Patients With Cutaneous Melanoma Receiving Immune Checkpoint Inhibitor Therapy

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

300

Start Date

2025-10-13

Completion Date

2027-06-30

Last Updated

2025-11-10

Healthy Volunteers

No

Interventions

PROCEDURE

Blood Sample

Blood samples will be collected

OTHER

Health Related Quality of Life Questionnaires (HRQoL)

Participants may be given HRQoLs during the course of data collection

OTHER

Medical Chart Review

Participants will undergo medical charts review during the course of data collection

Locations (1)

University of California, San Francisco

San Francisco, California, United States