Factors influencing the development of cutaneous squamous cell carcinoma in patients on BRAF inhibitor therapy

被引:32
作者
Anforth, Rachael [1 ,5 ]
Menzies, Alexander [5 ,6 ]
Byth, Karen [4 ]
Carlos, Giuliana [1 ,5 ]
Chou, Shaun [2 ]
Sharma, Raghwa [2 ,5 ,7 ]
Scolyer, Richard A. [5 ,6 ,8 ]
Kefford, Richard [3 ,5 ,6 ]
Long, Georgina V. [3 ,5 ,6 ]
Fernandez-Penas, Pablo [1 ,5 ]
机构
[1] Westmead Hosp, Dept Dermatol, Westmead, NSW 2145, Australia
[2] Westmead Hosp, Dept Tissue Pathol & Diagnost Oncol, Westmead, NSW 2145, Australia
[3] Westmead Hosp, Westmead Inst Canc Res, Westmead, NSW 2145, Australia
[4] Westmead Hosp, Res & Educ Network, Westmead, NSW 2145, Australia
[5] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[6] Melanoma Inst Australia, Sydney, NSW, Australia
[7] Univ Western Sydney, Fac Med, Penrith, NSW 1797, Australia
[8] Royal Prince Alfred Hosp, Tissue Pathol & Diagnost Oncol, Sydney, NSW, Australia
关键词
BRAF inhibitors; cutaneous squamous cell carcinoma; dabrafenib; melanoma; vemurafenib; DABRAFENIB GSK2118436; VERRUCAL KERATOSIS; RAS MUTATIONS; MELANOMA; SURVIVAL; FEATURES; TUMORS; V600E;
D O I
10.1016/j.jaad.2015.01.018
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: BRAF inhibitors (BRAFi) cause paradoxical activation of the MAPK pathway in keratinocytes resulting in cutaneous squamous cell carcinoma (cuSCC). Objective: We sought to examine the clinical factors involved in BRAFi-induced cuSCC development. Methods: We studied 134 patients with BRAF-mutant metastatic melanoma treated with a BRAFi at Westmead Hospital, Sydney, Australia. Details of cuSCC development and associations with melanoma clinicopathologic features and treatment outcome were examined. Results: In all, 32 (24%) patients developed 110 cuSCC after commencing treatment. In all, 61 (55%) cuSCC developed within the first 3 months. Age was the only independent risk factor for cuSCC development. After 3 months of therapy 4% of patients younger than 40 years developed cuSCC compared with 33% who were older than 60 years, and the hazard ratio of developing a cuSCC increased by 1.7 (95% confidence interval 1.3-2.3) per decade (P < .001). BRAFi cuSCC occurred more often in sun-protected areas (42%) compared with sporadic cuSCC (21%) (P < .001). cuSCC was not associated with progression-free survival. Limitations: The study was from a single center and patients were also at risk of sporadic cuSCC. Conclusion: Most BRAFi-induced cuSCC develop within 3 months of BRAFi therapy. The only independent risk factor is increasing age. cuSCC may present in anatomical locations with low ultraviolet exposure such that thorough dermatologic assessment is required.
引用
收藏
页码:809 / +
页数:8
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