Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Division of Oncology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Asian Pac J Allergy Immunol. 2019 Mar;37(1):12-18. doi: 10.12932/AP-140317-0047.
Several prospective studies have been conducted in epidermal growth factor receptor (EGFR) inhibitor-related cutaneous reactions in Caucasian patients, but prospective studies in Asian populations are scarce.
To investigate the cutaneous side effects of EGFR inhibitors in Asian cancer patients and to assess tumor response to dermatologic manifestations.
Sixty patients with lung or colorectal cancer who were receiving EGFR inhibitors were prospectively followed for at least one year by oncologists and dermatologists.
Of 60 patients (33 males, 27 females), 46 lung cancer patients received erlotinib (n=29) and gefitinib (n=17). Cetuximab was prescribed in 14 colorectal cancer patients. Fifty-eight patients (58/60, 96.7%) developed cutaneous reactions. The most common reactions were xerosis (82.8%), acne (79.3%), and skin desquamation (62.1%). Most reactions were mild and well-tolerated. Of 14 patients who had severe reactions, temporary treatment interruption was necessary in 3 patients and a decreasing dose was required in another 3 patients. There were no statistically significant differences in type, severity, or number of cutaneous reactions between responders (29/58) and non-responders (29/58) to EGFR inhibitors. At median follow-up time of 11.92±1.08 months, no patient died from cutaneous toxicities. Nine patients died from cancer and 11 patients lost to follow-up.
In this Asian population, almost all patients (96.7%) developed cutaneous toxicities of EGFR inhibitors. Xerosis, acne, and desquamation were common in Asian cancer patients. Most reactions were mild and well tolerated. Due to limited number of patients, this study did not show significant associations between cutaneous toxicities and tumor response.
已有多项针对白人表皮生长因子受体(EGFR)抑制剂相关皮肤反应的前瞻性研究,但亚洲人群的前瞻性研究却很少。
研究亚洲癌症患者接受 EGFR 抑制剂治疗的皮肤副作用,并评估皮肤表现与肿瘤应答的相关性。
由肿瘤学家和皮肤科医生对 60 例接受 EGFR 抑制剂治疗的肺癌或结直肠癌患者进行前瞻性随访,随访时间至少 1 年。
60 例患者(33 例男性,27 例女性)中,46 例肺癌患者接受厄洛替尼(n=29)和吉非替尼(n=17)治疗,14 例结直肠癌患者接受西妥昔单抗治疗。58 例(58/60,96.7%)患者出现皮肤反应。最常见的反应是皮肤干燥(82.8%)、痤疮(79.3%)和皮肤脱皮(62.1%)。大多数反应为轻度,且患者耐受良好。14 例出现严重反应的患者中,有 3 例需要暂时中断治疗,3 例需要减少剂量。EGFR 抑制剂应答者(29/58)和无应答者(29/58)的皮肤反应类型、严重程度和数量无统计学差异。在中位随访时间 11.92±1.08 个月时,无患者因皮肤毒性死亡。9 例患者因癌症死亡,11 例患者失访。
在本亚洲人群中,几乎所有患者(96.7%)均出现 EGFR 抑制剂的皮肤毒性。皮肤干燥、痤疮和脱皮在亚洲癌症患者中很常见。大多数反应为轻度且患者耐受良好。由于患者数量有限,本研究未显示皮肤毒性与肿瘤应答之间存在显著相关性。