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ABSTRACT: Purpose
Rash develops in approximately 50% of patients receiving alpelisib for breast cancer, often requiring dose modifications. Here, we describe the clinicopathologic, laboratory, and management characteristics of alpelisib-related dermatologic adverse events (dAEs).Methods
A single center-retrospective analysis was conducted. Data were abstracted from electronic medical records.Results
A total of 102 patients (mean age 56 years, range 27-83) receiving alpelisib most frequently in combination with endocrine therapy (79, 77.5%) were included. We identified 41 (40.2%) patients with all-grade rash distributed primarily along the trunk (78%) and extremities (70%) that developed approximately within two weeks of treatment initiation (mean 12.8 ± 1.5 days) and lasted o
SUBMITTER: Wang DG
PROVIDER: S-EPMC7398571 | biostudies-literature | 2020 Aug
REPOSITORIES: biostudies-literature