Giuliani Jacopo, Indelli Monica, Marzola Marina, Raisi Elena, Frassoldati Antonio
Clinical Oncology Unit, St Anna University Hospital, Ferrara, Italy.
Tumori. 2012 Jul-Aug;98(4):408-12. doi: 10.1177/030089161209800402.
Skin rash is a predictable and manageable side effect of anti-EGFR therapy such as cetuximab. The aim of this study is to estimate the costs for the foreseeable management of skin toxicity in patients treated with cetuximab in our institute in order to assess the direct medical economic impact.
We retrospectively analyzed all consecutive patients with advanced colorectal cancer treated with cetuximab at our institute from June 2006 to May 2011. We evaluated the severity and mean duration of skin rash for each grade and we identified the costs for the different therapeutic interventions. Patients were treated according to the general consensus management of skin toxicity associated with cetuximab treatment.
We evaluated 31 patients. The median follow-up was 28.95 months (range, 1.84-75.49). At last follow-up 10 patients (32.3%) were alive with metastases, 18 patients (58.1%) had died, 1 patient (3.2%) was alive without evidence of disease, and 2 patients (6.5%) were lost to follow-up. The median progression-free survival was 8.26 months and the median overall survival 32.89 months. Nineteen patients (61.3%) developed skin toxicities: 7 patients (22.6%) grade 1, 9 patients (29.0%) grade 2, 3 patients (9.7%) grade 3; no grade 4 skin toxicity was observed. The median duration of grade 1 toxicity was 79 days (no specific treatments were started), of grade 2 toxicity 95 days (cost range, € 199.50-294.50) and of grade 3 toxicity 64 days (cost range, € 159.42-233.90).
Our experience, through the analysis of nonselected cases, showed that the management of skin toxicities related to cetuximab is not so expensive. We recommend proper care of low-grade toxicities in order to reduce progression to high-grade toxicities and the resulting risk of hospitalization, which really impacts on costs.
皮疹是西妥昔单抗等抗表皮生长因子受体(EGFR)治疗可预测且可控制的副作用。本研究旨在估算我院接受西妥昔单抗治疗患者可预见的皮肤毒性管理成本,以评估直接医疗经济影响。
我们回顾性分析了2006年6月至2011年5月在我院接受西妥昔单抗治疗的所有连续性晚期结直肠癌患者。我们评估了每个等级皮疹的严重程度和平均持续时间,并确定了不同治疗干预措施的成本。患者按照与西妥昔单抗治疗相关的皮肤毒性的一般共识管理进行治疗。
我们评估了31例患者。中位随访时间为28.95个月(范围1.84 - 75.49个月)。在最后一次随访时,10例患者(32.3%)带转移灶存活,18例患者(58.1%)死亡,1例患者(3.2%)无疾病证据存活,2例患者(6.5%)失访。中位无进展生存期为8.26个月,中位总生存期为32.89个月。19例患者(61.3%)出现皮肤毒性:7例患者(22.6%)为1级,9例患者(29.0%)为2级,3例患者(9.7%)为3级;未观察到4级皮肤毒性。1级毒性的中位持续时间为79天(未开始特殊治疗),2级毒性为95天(成本范围199.50 - 294.50欧元),3级毒性为64天(成本范围159.42 - 233.90欧元)。
通过对非选择性病例的分析,我们的经验表明,西妥昔单抗相关皮肤毒性的管理成本并不高。我们建议对低级别毒性进行适当护理,以减少进展为高级别毒性以及由此导致的住院风险,这对成本有实际影响。