Dose escalation of ripretinib can lead to response in advanced gastrointestinal stromal tumor patients refractory to the standard dose: a report of two cases

P. A. Costa, Caroline Hana, N. Balaji, A. Skryd, Brianna Nicole Valdes, R. Minjares, Priscila Barreto-Coelho, Andrea P Espejo-Freire, Muhammad Hakim, Emily E. Jonczak, T. Subhawong, A. Livingstone, J. Trent, G. D'Amato
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引用次数: 2

Abstract

Despite an initial response, most metastatic gastrointestinal stromal tumor (GIST) patients will ultimately be refractory to all current therapies, including imatinib, sunitinib, and regorafenib. Ripretinib at 150 mg daily was recently approved as an additional line of treatment. Few options remain after ripretinib. Here we report two cases with responses to dose escalation of ripretinib after progressing on the standard dose. Case 1: A 25-year-old man was diagnosed with a kit exon 9 mutated small intestine GIST after presenting with abdominal pain. The tumor was resected, but a year later, he developed metastases to the liver and pelvis. Over the course of three years, he received multiple lines of therapies as his disease progressed, including imatinib, sunitinib, and regorafenib. He was then placed on ripretinib 150 mg daily. However, he had disease progression after two months. Ripretinib was increased to 150 mg twice a day, which he tolerated well. After three months, he had regression of his disease. Case 2: A 54-year-old male was diagnosed with an unresectable kit exon 11 mutated gastric GISTs after presenting with abdominal pain. Imatinib led to an 80% regression, allowing surgical excision. A year later, his disease recurred. Over the course of 5 years, due to multiple recurrences, he received two additional surgeries, with imatinib, sunitinib, regorafenib, and avapritinib on either the adjuvant or neoadjuvant setting. Ultimately, he developed a metastatic GIST to the left suprarenal region, retroperitoneum, and epigastric region. He was then started on ripretinib 150 mg daily, experiencing progression of his disease in three months. Ripretinib was escalated to 150 mg twice a day, which he tolerated well, and after three months, he had a regression. Dose escalation of ripretinib leads to response in patients that progressed after the standard dose, and it is well-tolerated, being a promising new treatment option in advanced GIST.
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利普雷替尼剂量递增可导致对标准剂量难治的晚期胃肠道间质瘤患者产生反应:两例报告
尽管最初有反应,但大多数转移性胃肠道间质瘤(GIST)患者最终对所有当前治疗都难以治愈,包括伊马替尼、舒尼替尼和瑞非尼。每日150毫克的利普雷替尼最近被批准作为一种额外的治疗方法。在利普雷替尼之后,几乎没有其他选择。在这里,我们报告了两个病例,在标准剂量进展后,对利普雷替尼剂量增加有反应。病例1:一名25岁的男子在出现腹痛后被诊断患有kit外显子9突变的小肠GIST。肿瘤被切除了,但一年后,他的肿瘤转移到了肝脏和骨盆。在三年中,随着病情的进展,他接受了多种治疗,包括伊马替尼、舒尼替尼和瑞戈非尼。然后给予每日150毫克的利普雷替尼。然而,他在两个月后病情恶化。利普雷替尼增加到150毫克,一天两次,他耐受良好。三个月后,他的病情有所好转。病例2:一名54岁男性在出现腹痛后被诊断为不可切除的kit外显子11突变胃gist。伊马替尼导致80%的消退,允许手术切除。一年后,他的病又复发了。在5年的时间里,由于多次复发,他接受了两次额外的手术,伊马替尼、舒尼替尼、瑞戈非尼和阿伐替尼作为辅助或新辅助治疗。最终,他发展为转移性间质瘤,转移至左肾上区、腹膜后和腹壁区域。随后,他开始服用每日150毫克的利普雷替尼,3个月后病情出现进展。利普雷替尼增加到150mg,每天两次,他耐受良好,三个月后,他的病情有所好转。利普雷替尼的剂量递增导致在标准剂量后进展的患者有反应,并且耐受性良好,是晚期GIST中有希望的新治疗选择。
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