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Cutaneous and Noncutaneous Adverse Effects in Patients with Advanced Melanoma Receiving Immunotherapy.
Yeung, Howa; Supapannachart, Krittin J; Francois, Sandy; Adler, Colin H; Kudchadkar, Ragini R; Lawson, David H; Yushak, Melinda L; Shariff, Afreen I; Chen, Suephy C.
Affiliation
  • Yeung H; Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Supapannachart KJ; Regional Telehealth Service, Veterans Integrated Service Network VISN 7, Atlanta, Georgia, USA.
  • Francois S; Department of Dermatology, University of California San Francisco, San Francisco, California, USA.
  • Adler CH; Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Kudchadkar RR; Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Lawson DH; Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Yushak ML; Winship Cancer Institute, Atlanta, Georgia, USA.
  • Shariff AI; Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Chen SC; Winship Cancer Institute, Atlanta, Georgia, USA.
JID Innov ; 3(6): 100232, 2023 Nov.
Article in En | MEDLINE | ID: mdl-38024559
ABSTRACT
Relationships between cutaneous adverse effects (CAEs) and noncutaneous adverse effects (NCAEs) of melanoma immunotherapy may help identify patterns tied to distinct immunologic pathways. The objective of this study was to determine the associations between CAEs and NCAEs among patients with stages III-IV melanoma receiving immunotherapy and who were enrolled in a prospective cohort. Electronic medical record data were abstracted from the first immunotherapy infusion until 1 year later. CAEs were rash or itch. NCAEs were symptoms and/or laboratory abnormalities documented as immunotherapy related. NCAE onset and time to NCAE were compared between participants with and without CAEs using ORs and Wilcoxon rank sum tests. Of 34 participants, 11 (32.4%) developed no adverse effects, 7 (20.1%) developed CAEs only, 3 (8.8%) developed NCAEs only, and 13 (38.2%) developed both CAEs and NCAEs. After adjustment for age, sex, and immunotherapy regimen, CAE was associated with higher odds of NCAE development (OR = 9.72; 95% confidence interval = 1.2-76.8). Median NCAE onset was 63 days in those with CAEs and 168 days in those without CAEs (P = 0.41). Limitations included a small sample size, and larger prospective studies should be performed to confirm findings. CAE was associated with NCAE development. Early identification and treatment of NCAEs may reduce symptom burden and hospitalizations associated with NCAEs.