Quality of Life Impact in Patients with Cutaneous Toxicities Caused by Epidermal Growth Factor Receptor Inhibitors and Immunotherapy

被引:1
作者
Mannino, Maria [1 ,2 ]
Sollena, Pietro [1 ]
Di Stefani, Alessandro [1 ]
Rossi, Ernesto [3 ]
D'Argento, Ettore [3 ]
Schinzari, Giovanni [3 ,4 ]
Tortora, Giampaolo [3 ,4 ]
Peris, Ketty [1 ,2 ]
机构
[1] Fdn Policlin Univ A Gemelli IRCCS, Dipartimento Sci Med & Chirurg, UO Dermatol, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Dipartimento Med & Chirurg Traslaz, Dermatol, Rome, Italy
[3] Fdn Policlin Univ Agostino Gemelli IRCCS, Med Oncol, Rome, Italy
[4] Univ Cattolica S Cuore, Med Oncol, Rome, Italy
关键词
Cutaneous toxicities; Quality of life; Epidermal growth factor receptor-inhibitors; Immunotherapy; DERMATOLOGICAL ADVERSE EVENTS; CLINICAL PRESENTATION; MANAGEMENT; NIVOLUMAB;
D O I
10.1159/000536332
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Novel oncologic therapies, including epidermal growth factor receptor inhibitors (EGFR-Is) and immune checkpoint inhibitors (ICIs), are associated with a new spectrum of adverse reactions, with prominent cutaneous toxicities. The impact of cutaneous adverse events (cAEs) on patients' quality of life (QoL) represents an unmet clinical need. Objectives: The aims of this study were (1) to assess whether cutaneous toxicities directed therapies are effective in reducing the QoL burden via the submission of 2 patient reported outcome measures (PROMs); (2) to investigate whether class of oncologic therapy, type of cAE and toxicity severity differently impact on patients' QoL. Methods: A prospective observational study was conducted at the Dermatology department of the Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, from October 2018 to October 2019. Patients aged >= 18 years, under therapy with EGFR-Is or ICIs and experiencing a treatment-related cAE were eligible for the study. Dermatology Life Quality Index (DLQI) and European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30 version 3.0 (EORTC QLQ-C30) were administered to patients at first clinical visit (T0), at 1-month (T1), and at 3-month (T2) dermatological follow-up. Results: Sixty cAEs of 51 patients have been recorded. A significant difference in the mean score for both DLQI and EORTC QLQ-C30 was found along the 3-months dermatological follow-up (p < 0.0001). A similar QoL improvement was reported for PROMs stratified by class of therapy and toxicity severity (p < 0.0001). No difference was reported for patients with pyogenic granuloma-like lesions and psoriasiform eruption as per DLQI. Class of therapy and toxicity severity did not differently impact on patients' QoL at selected timepoints; we reported a higher EORTC QLQ-C30 score at T2 for patients developing psoriasiform eruption compared to other types of cAEs. Conclusions: Early patients' referral to dermatologists and tailored management could result in better QoL. (c) 2024 S. Karger AG, Basel
引用
收藏
页码:523 / 530
页数:8
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