Su Xiao, Lacouture Mario E, Jia Yuxia, Wu Shenhong
Department of Medicine, AtlantiCare Regional Medical Center, Atlantic City, NJ, USA.
Oncology. 2009;77(2):124-33. doi: 10.1159/000229752. Epub 2009 Jul 22.
Cetuximab, a chimeric antibody against epidermal growth factor receptor has emerged as an effective therapy for advanced colorectal cancer (CRC) and head-neck cancer. However, severe skin toxicity may limit its use. Its efficacy in the treatment of other cancers is also undergoing extensive investigation. We performed a systemic review and meta-analysis of published clinical trials to quantify the overall incidence and risk of severe skin rash.
Databases Medline (OVID 1998 to July 2008), Web of Science, and abstracts presented at the American Society of Clinical Oncology conferences from 2004 through July 2008 were searched to identify relevant studies. Eligible studies include phase II and III clinical trials in which patients were treated with a single agent, i.e. cetuximab at 400 mg/m(2) as initial dose followed by 250 mg/m(2) weekly. Incidence, relative risk (RR), and 95% confidence intervals (CI) were calculated using a fixed-effects or random-effects model based on the heterogeneity of included studies.
A total of 2,037 patients with a variety of solid tumors from 16 trials were included for analysis. The overall incidence of all-grade skin rash was 88.2% (95% CI: 84.8-91.0%), with 11.3% (95% CI: 8.8-14.3%) being high-grade (grade 3 or above). The overall incidence of all-grade acne-like skin rash was 81.6% (95% CI: 75.4-86.6%) with 6.5% (95% CI: 4.1-10.0%) being high-grade. Notably, patients with CRC exhibited a significantly higher incidence of high-grade skin rash (12.6%, 95% CI: 9.7-16.4%) than those with non-CRC (6.6%, 95% CI: 3.6-11.8%) with a risk ratio of 1.9 (95% CI: 1.0-3.6, p = 0.049). From randomized controlled studies, patients who received cetuximab had a significantly increased risk of developing high-grade skin rash in comparison with controls (RR 21.8, 95% CI: 6.9-68.8, p < 0.001).
Cancer patients who received cetuximab have a substantial risk of developing high-grade skin rash. The risk may be particularly increased in patients with CRC. Further studies are strongly recommended for the prevention and treatment of high-grade skin rash.
西妥昔单抗是一种针对表皮生长因子受体的嵌合抗体,已成为晚期结直肠癌(CRC)和头颈癌的有效治疗方法。然而,严重的皮肤毒性可能会限制其使用。其在治疗其他癌症方面的疗效也在进行广泛研究。我们对已发表的临床试验进行了系统评价和荟萃分析,以量化严重皮疹的总体发生率和风险。
检索数据库Medline(OVID 1998年至2008年7月)、科学网以及2004年至2008年7月在美国临床肿瘤学会会议上发表的摘要,以确定相关研究。符合条件的研究包括II期和III期临床试验,其中患者接受单一药物治疗,即初始剂量为400mg/m²的西妥昔单抗,随后每周250mg/m²。根据纳入研究的异质性,使用固定效应或随机效应模型计算发生率、相对风险(RR)和95%置信区间(CI)。
共纳入16项试验中的2037例患有各种实体瘤的患者进行分析。所有级别皮疹的总体发生率为88.2%(95%CI:84.8 - 91.0%),其中11.3%(95%CI:8.8 - 14.3%)为高级别(3级或以上)。所有级别痤疮样皮疹的总体发生率为81.6%(95%CI:75.4 - 86.6%),其中6.5%(95%CI:4.1 - 10.0%)为高级别。值得注意的是,CRC患者的高级别皮疹发生率(12.6%,95%CI:9.7 - 16.4%)显著高于非CRC患者(6.6%,9%CI:3.6 - 11.8%),风险比为1.9(95%CI:1.0 - 3.6,p = 0.049)。从随机对照研究来看,与对照组相比,接受西妥昔单抗治疗的患者发生高级别皮疹的风险显著增加(RR 21.8,95%CI:6.9 - 68.8,p < 0.001)。
接受西妥昔单抗治疗的癌症患者发生高级别皮疹的风险很大。CRC患者的风险可能尤其增加。强烈建议进一步研究高级别皮疹的预防和治疗。