Okajima Masaaki, Miura Satoru, Watanabe Satoshi, Tanaka Hiroshi, Ito Kazuhiko, Ishida Takashi, Makino Masato, Iwashima Akira, Matsumoto Naoya, Sato Kazuhiro, Ichikawa Kosuke, Abe Tetsuya, Yoshizawa Hirohisa, Kikuchi Toshiaki
Department of Respiratory Medicine, Saiseikai Niigata Hospital, Niigata, Japan.
Department of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan.
Transl Lung Cancer Res. 2021 Jan;10(1):252-260. doi: 10.21037/tlcr-20-649.
Afatinib has shown clinical benefits in patients with non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor () mutations. Many patients treated with afatinib experience skin or gastrointestinal toxicity. However, an effective management strategy has not been established. This prospective study was conducted to evaluate the efficacy of multimodal prophylactic treatment for afatinib-induced toxicity.
This single-arm prospective study was conducted to evaluate the efficacy of multimodal prophylactic treatment for afatinib-induced toxicity in patients with mutation positive advanced NSCLC who planned to receive a 40 mg dose of afatinib. Eligible patients were treated with oral loperamide (2 mg twice per day), prophylactic minocycline (100 mg once per day), topical medium-class steroids, and gargling with sodium azulene. The primary endpoint was the ability of prophylactic loperamide to prevent severe or intolerable diarrhea during the 4 weeks after the initial administration of afatinib. The incidence, severity and time to occurrence of diarrhea, rash, oral mucositis and paronychia were evaluated based on a daily patient questionnaire.
Forty-six patients were enrolled. The primary endpoint analysis was performed in 35 patients as the per-protocol (PP) population. The 4-week successful prophylaxis rate for severe or intolerable diarrhea was 82.9% (90% confidence interval: 70.1-91.9%). In the total population, the incidences of grade 3 or higher rash, oral mucositis and paronychia within 4 weeks were 4%, 2% and 4%, respectively.
Prophylactic loperamide administration was not effective in preventing severe or intolerable diarrhea during afatinib treatment. Adequate dose reduction will be a better approach to manage afatinib-induced diarrhea. Multimodal prevention using minocycline, topical steroids and gargling with sodium azulene may be helpful to maintain compliance with afatinib treatment (UMIN000016167).
阿法替尼已在携带表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者中显示出临床获益。许多接受阿法替尼治疗的患者会出现皮肤或胃肠道毒性。然而,尚未建立有效的管理策略。本前瞻性研究旨在评估多模式预防性治疗对阿法替尼诱导毒性的疗效。
本单臂前瞻性研究旨在评估多模式预防性治疗对计划接受40mg剂量阿法替尼治疗的EGFR突变阳性晚期NSCLC患者阿法替尼诱导毒性的疗效。符合条件的患者接受口服洛哌丁胺(每日2次,每次2mg)、预防性米诺环素(每日1次,每次100mg)、局部中效类固醇以及用薁磺酸钠含漱。主要终点是预防性洛哌丁胺在首次给予阿法替尼后4周内预防严重或无法耐受腹泻的能力。根据每日患者问卷评估腹泻、皮疹、口腔黏膜炎和甲沟炎的发生率、严重程度及发生时间。
共纳入46例患者。作为符合方案(PP)人群,对35例患者进行了主要终点分析。严重或无法耐受腹泻的4周成功预防率为82.9%(90%置信区间:70.1 - 91.9%)。在总体人群中,4周内3级或更高等级皮疹、口腔黏膜炎和甲沟炎的发生率分别为4%、2%和4%。
预防性给予洛哌丁胺在预防阿法替尼治疗期间严重或无法耐受腹泻方面无效。适当降低剂量可能是管理阿法替尼诱导腹泻的更好方法。使用米诺环素、局部类固醇以及用薁磺酸钠含漱的多模式预防可能有助于维持对阿法替尼治疗的依从性(UMIN000016167)。