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瑞普替尼:四线或后线治疗胃肠间质瘤的研究进展。

Ripretinib: A Review in Gastrointestinal Stromal Tumours as Fourth-or Later-Line of Therapy.

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2022 Oct;82(15):1541-1548. doi: 10.1007/s40265-022-01794-0. Epub 2022 Oct 25.

Abstract

Ripretinib (Qinlock) is a small molecule inhibitor of the receptor tyrosine kinases KIT and platelet-derived growth factor receptor α (PDGFRA) and is approved for the treatment of gastrointestinal stromal tumours as a fourth-line of therapy. After successive cycles of treatment, gastrointestinal stromal tumours can carry a wide array of mutations, which makes resistance to treatment more likely. Ripretinib has a dual mechanism of action that allows it to target a broad spectrum of mutations in KIT or PDGFRA. The pivotal phase III INVICTUS trial demonstrated an increase of progression-free survival in patients receiving ripretinib compared with placebo, with efficacy being maintained across patients with KIT exon 9, 11, 13 and 17 mutations. Ripretinib has acceptable tolerability, with the most common drug-related grade 3 or 4 adverse events being lipase increases, hypertension, fatigue and hypophosphataemia. Ripretinib is therefore a valuable additional line of therapy available for the management of gastrointestinal stromal tumours.

摘要

瑞普替尼(Qinlock)是一种小分子抑制剂,可抑制受体酪氨酸激酶 KIT 和血小板衍生生长因子受体α(PDGFRA),被批准用于治疗胃肠道间质瘤的四线治疗。经过连续的治疗周期后,胃肠道间质瘤可能会携带多种突变,从而更有可能对治疗产生耐药性。瑞普替尼具有双重作用机制,可靶向 KIT 或 PDGFRA 的广泛突变。关键的 III 期 INVICTUS 试验表明,与安慰剂相比,接受瑞普替尼治疗的患者无进展生存期延长,并且在 KIT 外显子 9、11、13 和 17 突变的患者中疗效得以维持。瑞普替尼具有可接受的耐受性,最常见的药物相关 3 级或 4 级不良事件为脂肪酶升高、高血压、疲劳和低磷血症。因此,瑞普替尼是胃肠道间质瘤治疗的一种有价值的额外治疗选择。

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