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Mixed response and mechanisms of resistance to larotrectinib in metastatic carcinoma ex pleomorphic adenoma of the parotid harboring an NTRK2 fusion

机译:在植物中患有NTRK2融合的植物癌中的抗泌乳癌中抗泌乳胰蛋白抗性的混合反应及其机制

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INTRODUCTION:Standardized systemic treatment options are lacking for carcinoma ex pleomorphic adenoma, which is a rare and aggressive tumor primarily found in salivary glands.Here we report the case of a 63-year-old male with carcinoma ex pleomorphic adenoma of the left parotid and parapharyngeal space harboring a neurotrophic receptor tyrosine kinase (NTRK) 2 fusion who was treated with a small molecule inhibitor that targets the tropomyosin receptor kinase (TRK) proteins. To the best of our knowledge, no similar case has been described in the literature so far.PATIENT CONCERNS:After multiple surgical resections and radiotherapy for localized cancer disease over several years, our patient again developed an increasing swelling and pain around the left ear and numbness of the left half of the face.DIAGNOSIS:Magnetic resonance imaging and positron emission tomography/computed tomography scans showed tumor recurrence in the left parotid, below the left ear, and in the parapharyngeal space, as well as metastases of the lungs and cervical lymph nodes. As data on the efficacy of systemic therapies for inoperable carcinoma ex pleomorphic adenoma are scarce, we performed a next-generation sequencing that revealed the presence of a hitherto unknown NTRK2 fusion.INTERVENTIONS:Treatment with the TRK inhibitor larotrectinib was initiated, which induced rapid symptom improvement. However, part of the tumor had to be removed shortly afterwards due to local progression. Molecular testing did not demonstrate any alterations accounting for resistance to larotrectinib, with maintenance of the NTRK2 fusion.OUTCOMES:Three months later, imaging confirmed mixed response. While the reason for this remains unknown, the patient is in good condition and continues to receive larotrectinib.CONCLUSION:It remains unclear why our patient showed mixed response to larotrectinib and further studies are needed to explore other possible mechanisms of resistance.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:介绍:缺乏标准化的全身治疗选择,癌患者是一种稀有和激进的肿瘤,主要是唾液腺。我们举报了63岁男性的案件,伴有左侧腮腺腺癌含有神经营养受体酪氨酸激酶(NTRK)2融合的映静脉膜空间用靶向靶向刺激素受体激酶(TRK)蛋白的小分子抑制剂治疗。据我们所知,文献中没有类似的情况。迄今为止,患者担心左半部分的麻木。磁共振成像和正电子排放断层扫描/计算机断层扫描扫描显示左耳静脉曲张的肿瘤复发,在左耳以下,以及肺部和颈椎的转移淋巴结。由于数据疗法的疗效是不可操作的癌患者的数据稀缺,我们进行了下一代测序,揭示了迄今未知的NTRK2融合的存在。Interventions:启动与Trk抑制剂Larotrecinib的治疗,这诱导了快速症状改进。然而,由于局部进展,不久之后,必须尽快去除一部分肿瘤。分子试验没有展示任何改变核算耐什么蜥蜴的抵抗力,维持NTRK2融合。提示:三个月后,成像确认的混合反应。虽然这遗骸的原因未知,但患者状况良好并继续接受Larotrectinib.Conclusion:仍然尚不清楚为什么我们的患者表现出对Larotrectinib的混合反应以及进一步的研究来探索其他可能的抵抗机制。 2021提交人。由Wolters Kluwer Health,Inc。出版

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