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AXL184 在头颈部上呼吸消化道复发性和/或转移性唾液腺癌的 II 期试验。

Phase II trial with axitinib in recurrent and/or metastatic salivary gland cancers of the upper aerodigestive tract.

机构信息

Head and Neck Medical Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Radiology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

出版信息

Head Neck. 2019 Oct;41(10):3670-3676. doi: 10.1002/hed.25891. Epub 2019 Jul 29.

Abstract

BACKGROUND

Patients with prognosis recurrent/metastatic (R/M) salivary gland carcinomas (SGCs) are poor. Activity of axitinib was demonstrated in adenoid cystic carcinoma (ACC). We tested axitinib in a larger cohort of R/M SGCs including non-ACC.

METHODS

Axitinib was administered at 10 mg daily (dose escalation allowed) until progression or unacceptable toxicity. Null hypothesis would be rejected if more than 3 of 26 responses were observed.

RESULTS

Twenty-six patients (50% were male; 6 ACC, 20 non-ACC) were treated. Response rate was 8% (2 partial responses), 13 stable disease (>6 months in 7 patients) and 11 disease progression. Median progression-free survival and overall survival were 5.5 and 26.2 months, respectively. All patients had at least one adverse event: stomatitis (69%), fatigue (58%) and hypertension (54%) were the most frequent.

CONCLUSIONS

This trial did not meet its primary endpoint hence axitinib should not be considered for further investigations in SGCs. Safety profile was in line with the scientific literature.

摘要

背景

预后复发/转移性(R/M)涎腺癌(SGC)患者的情况较差。阿昔替尼在腺样囊性癌(ACC)中表现出活性。我们在包括非 ACC 的更大 R/M SGC 队列中测试了阿昔替尼。

方法

阿昔替尼每天 10mg 给药(允许剂量递增),直到疾病进展或出现不可接受的毒性。如果观察到超过 26 个反应中的 3 个,则会拒绝零假设。

结果

26 名患者(50%为男性;6 名 ACC,20 名非 ACC)接受了治疗。反应率为 8%(2 名部分缓解),13 名病情稳定(7 名患者病情稳定超过 6 个月),11 名病情进展。中位无进展生存期和总生存期分别为 5.5 和 26.2 个月。所有患者均至少出现一次不良事件:口腔炎(69%)、疲劳(58%)和高血压(54%)是最常见的。

结论

本试验未达到主要终点,因此阿昔替尼不应考虑进一步用于 SGC 的研究。安全性特征与科学文献一致。

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