Epidermal growth factor receptor inhibitors in advanced cutaneous squamous cell carcinoma: A systematic review and meta-analysis

被引:1
|
作者
Pham, James P. [1 ,2 ]
Rodrigues, Anthony [1 ,2 ]
Goldinger, Simone M. [3 ]
Sim, Hao-Wen [1 ,2 ,4 ]
Liu, Jia [1 ,2 ,5 ,6 ]
机构
[1] St Vincents Hosp Sydney, Dept Med Oncol, Darlinghurst, NSW, Australia
[2] UNSW Med & Hlth, Sch Clin Med, St Vincents Clin Campus, Darlinghurst, NSW, Australia
[3] Univ Hosp Zurich, Dept Dermatol, Zurich, Switzerland
[4] Univ Sydney, NHMRC Clin Trials Ctr, Camperdown, NSW, Australia
[5] Univ Sydney, Fac Med & Hlth, Sydney, NSW, Australia
[6] Kinghorn Canc Ctr, Dept Med Oncol, 370 Victoria St, Darlinghurst, NSW 2010, Australia
关键词
cutaneous squamous cell carcinoma; EGFR; epidermal growth factor receptor inhibitor; SCC; PHASE-II; CETUXIMAB; EFFICACY; GEFITINIB; THERAPY; CANCER;
D O I
10.1111/exd.14978
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Patients with advanced cutaneous squamous cell carcinoma (cSCC) who are not eligible for or who fail to respond to anti-PD1 immunotherapy have few treatment options. Epidermal growth factor receptor (EGFR) inhibitors have been investigated as a therapeutic option for advanced cSCC; however, data are limited to small single-arm trials or retrospective studies. A systematic review and meta-analysis was conducted to PRISMA guidelines (CRD42023394300). Studies reporting on outcomes of EGFR inhibition in advanced cSCC were identified. Objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and adverse event (AE) rate were pooled using a random effects model and the inverse variance method. Twelve studies (six prospective, six retrospective) were identified, representing 324 patients. Pooled ORR was 26% (95% confidence interval [CI] 18-36), median PFS was 4.8 months (95% CI 3.9-6.6) and median OS was 11.7 months (95% CI 9.2-14.1). Any grade AEs occurred in 93% of patients (95% CI 85-97) while grade 3 and higher AEs occurred in 30% (95% CI 14-54). These results were similar between anti-EGFR monoclonal antibodies (MAbs) and tyrosine kinase inhibitors (TKIs). EGFR inhibitors can be considered in patients with advanced cSCC who are contraindicated for or progress on first-line anti-PD1 immunotherapy. Future studies should evaluate their activity and safety following anti-PD1, identify predictive biomarkers for their efficacy and explore combination approaches.
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页数:7
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