Monoclonal antibody-induced papulopustular rash: Clinical course, communication to health-care professionals and reactive measures as reported by patients

被引:0
|
作者
Cignola, Sara [1 ]
Gonella, Silvia [2 ]
Alessandra, Bin [3 ]
Palese, Alvisa [1 ,4 ]
机构
[1] Univ Udine, Sch Nursing, Viale Ungheria 20, I-33100 Udine, Italy
[2] Univ Verona, Dept Publ Hlth & Community Med, I-37100 Verona, Italy
[3] Teaching Hosp, Dept Oncol, Udine, Italy
[4] Univ Udine, Dept Med & Biol Sci, I-33100 Udine, Italy
关键词
Monoclonal antibodies; Receptor; Epidermal Growth Factor; Skin diseases; Nursing care; Patient education; Skin rash; CELL LUNG-CANCER; ADVANCED COLORECTAL-CANCER; SKIN TOXICITY; PHASE-II; DERMATOLOGICAL TOXICITIES; CETUXIMAB; MANAGEMENT; TRIAL; CHEMOTHERAPY; ERLOTINIB;
D O I
10.1016/j.ejon.2015.07.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The primary end-point was to describe the clinical course of monoclonal antibody-induced papulopustular rash (mAB-induced PPR), when patients alert health-care providers and the subsequent reactive measures employed. Exploring the predictors affecting PPR grading was the secondary end-point. Methods: A multicentre retrospective study involving six Italian oncology outpatient departments was conducted. Thirty-nine patients with cancer undergoing cetuximab or panitumumab treatment were included. Information was collected through medical records and face-to-face interviews. mAB-induced PPR was scored by patients' self-reported Common Terminology Criteria for Adverse Eventsv4.02 and was defined as severe when the grade >= 3. Results: Thirty-five (89.7%) patients developed a rash, which was severe in nine cases. The rash usually appeared within the first week after starting the drug (22, 62.8%), peaked in severity during the first month (26, 74.3%) and resolved 4-8 weeks after the end of mABs therapy (15, 45.7%). At the time of the interviews, the rash was not still resolved in almost half (n = 16) of the patients. Twenty-six (74.3%) patients reported sequelae and the mostly common were erythema (21, 81%) and dry skin (14, 54%). Only half of the patients informed health-care professionals as soon as the rash appeared. All the patients treated the rash topically and mAB therapy was modified in 16 (45.7%) cases (reduction, n = 10; discontinuation, n = 9; withdrawal, n = 2). No association between male gender, age, fair skin, current smokers during therapy and PPR grading escalation was found. Conclusions: The clinical course of the rash was pathognomonic. Patients should be further encouraged to communicate the onset of a rash to health-care professionals as soon as it appears to avoid grading escalation and sequelae. The adoption of CTCAE as a patient-reported outcome may become an instrument to help health-care providers in tailoring treatment measures. (C) 2015 Elsevier Ltd. All rights reserved.
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页码:133 / 139
页数:7
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