Erlotinib-associated rash in patients with EGFR mutation-positive non-small-cell lung cancer treated in the EURTAC trial

被引:8
|
作者
de Marinis, Filippo [1 ,2 ]
Vergnenegre, Alain [3 ]
Passaro, Antonio [1 ,2 ]
Dubos-Arvis, Catherine [4 ]
Carcereny, Enric [5 ]
Drozdowskyj, Ana [6 ]
Zeaiter, Ali [7 ]
Perez-Moreno, Pablo [7 ]
Rosell, Rafael [5 ]
机构
[1] European Inst Oncol, Div Thorac Oncol, Milan, Italy
[2] High Specializat Hosp, Rome, Italy
[3] CHU Limoges, Hop Cluzeau, Limoges, France
[4] Ctr Francois Baclesse, F-14021 Caen, France
[5] Hosp Badalona Germans Trias & Pujol, Catalan Inst Oncol, Badalona, Spain
[6] Pivotal SL, Madrid, Spain
[7] F Hoffmann La Roche, Basel, Switzerland
关键词
EGFR; erlotinib; non-small-cell lung cancer; rash; safety; QUALITY-OF-LIFE; OPEN-LABEL; PHASE-III; CUTANEOUS TOXICITIES; 1ST-LINE TREATMENT; SKIN TOXICITIES; CHEMOTHERAPY; MULTICENTER; CARBOPLATIN; CTONG-0802;
D O I
10.2217/fon.14.269
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: This analysis investigates incidence and time course of rash in the EURTAC study. Materials & methods: Patients with EGFR mutation-positive non-small-cell lung cancer were randomized 1:1 to receive once daily erlotinib or 3-weekly cycles of chemotherapy. Results: Of the 86 erlotinib-treated patients, 71 reported rash. Median time to first rash appearance was 0.7 months. Most patients (n = 65) had the same or lower grade rash at final assessment compared with initial assessment. Of the 21 patients with decreased rash grade between initial and final assessments, 61.9% received no erlotinib dose modification, 42.8% had no concomitant rash treatment. Conclusion: Most rash cases were mild, occurred within 1 month of erlotinib treatment, and rapidly improved without the need for erlotinib dose alterations.
引用
收藏
页码:421 / 429
页数:9
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