Cutaneous and Noncutaneous Adverse Effects in Patients with Advanced Melanoma Receiving Immunotherapy

Howa Yeung , Krittin J. Supapannachart , Sandy Francois , Colin H. Adler , Ragini R. Kudchadkar , David H. Lawson , Melinda L. Yushak , Afreen I. Shariff , Suephy C. Chen
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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.

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接受免疫治疗的晚期黑色素瘤患者的皮肤和非皮肤不良反应
黑色素瘤免疫治疗的皮肤不良反应(CAEs)和非皮肤不良反应(NCAEs)之间的关系可能有助于识别与不同免疫途径相关的模式。本研究的目的是确定在接受免疫治疗的III-IV期黑色素瘤患者中cae和ncae之间的关系,这些患者被纳入前瞻性队列。从第一次免疫治疗输注到1年后的电子病历数据提取。CAEs为皮疹或瘙痒。NCAEs是经证实与免疫治疗相关的症状和/或实验室异常。使用or和Wilcoxon秩和检验比较有和无cae的受试者的NCAE发病和NCAE发生时间。在34名参与者中,11名(32.4%)没有出现不良反应,7名(20.1%)仅发生CAEs, 3名(8.8%)仅发生NCAEs, 13名(38.2%)同时发生CAEs和NCAEs。在调整了年龄、性别和免疫治疗方案后,CAE与NCAE发生的较高几率相关(OR = 9.72;95%置信区间= 1.2-76.8)。有cae组NCAE发病的中位时间为63天,无cae组为168天(P = 0.41)。局限性包括样本量小,需要进行更大规模的前瞻性研究来证实研究结果。CAE与NCAE的发展相关。早期发现和治疗NCAEs可以减少与NCAEs相关的症状负担和住院。
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审稿时长
8 weeks
期刊最新文献
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