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阿法替尼低起始剂量在10例老年或低体能状态的晚期难治性非小细胞肺癌患者中的耐受性和疗效

Tolerability and efficacy of afatinib at a low starting dosage in 10 elderly or low performance status patients with advanced refractory non-small-cell lung cancer.

作者信息

Kashiwabara Kosuke, Semba Hiroshi, Fujii Shinji, Tsumura Shinsuke

机构信息

Department of Respiratory Medicine, Kumamoto Regional Medical Center, 5-16-10 hon-jo, Kumamoto, 860-0811, Japan.

Department of Respiratory Medicine, Kumamoto Regional Medical Center, 5-16-10 hon-jo, Kumamoto, 860-0811, Japan.

出版信息

Respir Investig. 2016 Nov;54(6):468-472. doi: 10.1016/j.resinv.2016.06.007. Epub 2016 Aug 25.

Abstract

BACKGROUND

Whether a full dosage of afatinib is tolerable and effective for elderly or low performance status (PS) patients with advanced refractory non-small-cell lung cancer (NSCLC) is unclear.

METHODS

We retrospectively evaluated the tolerability and efficacy of afatinib in 10 patients (the majority elderly) with a low PS score (2 or 3), who had advanced refractory adenocarcinoma and were carrying active epidermal growth factor receptor mutations. Afatinib was administered at a starting dosage of 20 or 30mg/day, followed by 10mg increases in dose up to a maximum dosage of 40mg/day.

RESULTS

The median patient age was 76 years and 50% of the patients had a PS of 3. The patients had previously been treated with gefitinib and/or erlotinib, with a median number of three chemotherapy regimens. All the patients received at least 30mg/day of afatinib. Eight patients did not receive the 40mg/day dosage because of patient refusal due to grade 2 diarrhea (n=6) or the judgment of the doctor (n=2). One patient discontinued the treatment because of drug-induced interstitial lung disease. The most frequent adverse event was grade 2 diarrhea. The objective response rate was 11% and the PS score of five cases improved after afatinib therapy. The median progression-free survival and overall survival periods were 3.6 months and 5.8 months, respectively.

CONCLUSIONS

A low starting dosage of afatinib might enable elderly or low PS patients with advanced refractory NSCLC to receive this drug as salvage therapy.

摘要

背景

对于老年或体能状态(PS)较差的晚期难治性非小细胞肺癌(NSCLC)患者,阿法替尼全剂量是否可耐受且有效尚不清楚。

方法

我们回顾性评估了10例PS评分较低(2或3分)、患有晚期难治性腺癌且携带活性表皮生长因子受体突变的患者(大多数为老年人)使用阿法替尼的耐受性和疗效。阿法替尼起始剂量为20或30mg/天,随后每次增加10mg剂量,直至最大剂量40mg/天。

结果

患者中位年龄为76岁,50%的患者PS评分为3分。这些患者之前接受过吉非替尼和/或厄洛替尼治疗,中位化疗方案数为三种。所有患者均接受了至少30mg/天的阿法替尼治疗。8例患者未接受40mg/天的剂量,其中6例因2级腹泻患者拒绝,2例因医生判断。1例患者因药物性间质性肺病停药。最常见的不良事件是2级腹泻。客观缓解率为11%,5例患者经阿法替尼治疗后PS评分改善。中位无进展生存期和总生存期分别为3.6个月和5.8个月。

结论

低起始剂量的阿法替尼可能使老年或PS较差的晚期难治性NSCLC患者能够接受该药作为挽救治疗。

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