首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >A phase II study of sunitinib in recurrent and/or metastatic adenoid cystic carcinoma (ACC) of the salivary glands: Current progress and challenges in evaluating molecularly targeted agents in ACC
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A phase II study of sunitinib in recurrent and/or metastatic adenoid cystic carcinoma (ACC) of the salivary glands: Current progress and challenges in evaluating molecularly targeted agents in ACC

机译:舒尼替尼在唾液腺复发和/或转移性腺样囊性癌(ACC)中的II期研究:评估ACC中分子靶向药物的当前进展和挑战

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Background: Vascular endothelial growth factor (VEGF) and c-kit are highly expressed in adenoid cystic carcinoma (ACC) and associated with biologic aggressiveness. This study aimed to assess the antitumor activity of sunitinib, a multi-targeted inhibitor of vascular endothelial growth factor receptor, c-kit, platelet-derived growth factor receptor, ret proto-oncogene (RET) and FMS-like tyrosine kinase 3 (FLT3), in ACC of the salivary gland. Patients and methods: Patients with progressive, recurrent and/or metastatic ACC were treated with sunitinib 37.5 mg daily in this single-arm, two-stage phase II trial. Response was assessed every 8 weeks. Results: Fourteen patients were enrolled on to the study. Among 13 assessable patients, there were no objective responses, 11 patients had stable disease (SD), 8 patients had SD >6 months and 2 patients had progressive disease as best response. Median time toprogressionwas 7.2 months. Median overall survivalwas 18.7 months. Toxic effects occurring in at least 50% of patients included fatigue, oral mucositis and hypophosphatemia usually of mild to moderate severity. Conclusions: Although no responses were observed, sunitinib was well tolerated, with prolonged tumor stabilization of >6 months in 62% of assessable patients. The lack of responses is comparable with other trials of molecularly targeted agents in ACC and highlights the need for novel strategies in phase II clinical trial design.
机译:背景:血管内皮生长因子(VEGF)和c-kit在腺样囊性癌(ACC)中高度表达,并与生物学侵袭性相关。这项研究旨在评估舒尼替尼的抗肿瘤活性,舒尼替尼是血管内皮生长因子受体,c-kit,血小板源性生长因子受体,ret原癌基因(RET)和FMS样酪氨酸激酶3(FLT3)的多靶点抑制剂),在唾液腺的ACC中。患者和方法:在该单臂,二阶段的II期临床试验中,每天用37.5 mg舒尼替尼治疗患有进行性,复发和/或转移性ACC的患者。每8周评估一次反应。结果:14名患者被纳入研究。在13例可评估患者中,没有客观反应,11例疾病稳定(SD),8例SD> 6个月,2例疾病进展为最佳反应。进步的中位数时间是7.2个月。中位总生存期为18.7个月。至少50%的患者发生的毒性作用包括疲劳,口腔粘膜炎和低磷血症,通常轻度至中度。结论:尽管未观察到反应,舒尼替尼耐受性良好,在62%的可评估患者中,肿瘤稳定期延长了> 6个月。缺乏反应与ACC中针对分子靶向药物的其他试验具有可比性,并突出了II期临床试验设计中对新策略的需求。

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