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间变性甲状腺癌的新型治疗方法。

Novel treatments for anaplastic thyroid carcinoma.

作者信息

Ferrari Silvia Martina, Elia Giusy, Ragusa Francesca, Ruffilli Ilaria, La Motta Concettina, Paparo Sabrina Rosaria, Patrizio Armando, Vita Roberto, Benvenga Salvatore, Materazzi Gabriele, Fallahi Poupak, Antonelli Alessandro

机构信息

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Department of Pharmacy, University of Pisa, Pisa, Italy.

出版信息

Gland Surg. 2020 Jan;9(Suppl 1):S28-S42. doi: 10.21037/gs.2019.10.18.

Abstract

Anaplastic thyroid cancer (ATC) is one of the deadliest human cancers and it is less than 2% of thyroid carcinomas (TCs). The standard treatment of ATC includes surgical debulking, accelerated hyperfractionated external beam radiation therapy (EBRT), and chemotherapy, in particular with cisplatin or doxorubicin, achieving about 10 months of median survival. Since ATC is a rare and aggressive tumor, it is still challenging to predict the patient clinical therapy responsiveness. Several genetic mutations have been described in ATC, involved in different molecular pathways linked to tumor progression, and novel therapies acting on these molecular pathways have been investigated, to improve the quality of life in these patients. Here we review the new targeted therapy of ATC. We report interesting results obtained with molecules targeting different pathways: angiogenesis (vandetanib, combretastatin, sorafenib, lenvatinib, sunitinib, CLM94, CLM3, etc.); EGFR (gefitinib, docetaxel); BRAF (dabrafenib/trametinib, vemurafenib); PPARγ agonists (rosiglitazone, pioglitazone, efatutazone); PD-1 and PD-L1 (pembrolizumab); TERT. To escape resistance to monotherapies, the evaluation of combination strategies with radiotherapy, chemotherapy, or targeted drugs is ongoing. The results of clinical trials with dabrafenib and trametinib led to the approval from FDA of this combination for patients with BRAF V600E mutated ATC with locally advanced, unresectable, or metastatic ATC. The anti-PD-L1 antibody immunotherapy, alone or combined with a BRAF inhibitor, has been shown also promising in the treatment of ATC. Furthermore, to increase the therapeutic success and not to use ineffective or even harmful treatments, a real tailored therapy should be pursued, and this can be achieved thanks to the new available genomic analysis methods and to the possibility to test in vitro novel treatments directly in primary cells from each ATC patient. Exploring new treatment strategies is mandatory to improve the survival of these patients, guaranteeing a good quality of life.

摘要

间变性甲状腺癌(ATC)是最致命的人类癌症之一,占甲状腺癌(TC)的比例不到2%。ATC的标准治疗包括手术减瘤、加速超分割外照射放疗(EBRT)和化疗,特别是使用顺铂或阿霉素,中位生存期约为10个月。由于ATC是一种罕见且侵袭性强的肿瘤,预测患者的临床治疗反应仍然具有挑战性。ATC中已描述了几种基因突变,这些突变涉及与肿瘤进展相关的不同分子途径,并且已经研究了作用于这些分子途径的新型疗法,以改善这些患者的生活质量。在此,我们综述ATC的新靶向治疗。我们报告了用靶向不同途径的分子获得的有趣结果:血管生成(凡德他尼、考布他汀、索拉非尼、乐伐替尼、舒尼替尼、CLM94、CLM3等);表皮生长因子受体(EGFR)(吉非替尼、多西他赛);BRAF(达拉非尼/曲美替尼、维莫非尼);过氧化物酶体增殖物激活受体γ(PPARγ)激动剂(罗格列酮、吡格列酮、依伐他汀);程序性死亡受体1(PD-1)和程序性死亡配体1(PD-L1)(帕博利珠单抗);端粒酶逆转录酶(TERT)。为了避免对单一疗法产生耐药性,正在评估放疗、化疗或靶向药物联合策略。达拉非尼和曲美替尼的临床试验结果导致美国食品药品监督管理局(FDA)批准该联合疗法用于治疗BRAF V600E突变的局部晚期、不可切除或转移性ATC患者。抗PD-L1抗体免疫疗法单独或与BRAF抑制剂联合使用,在ATC治疗中也显示出前景。此外,为了提高治疗成功率且不使用无效甚至有害的治疗方法,应采用真正的个体化治疗,这可以通过新的可用基因组分析方法以及直接在每个ATC患者的原代细胞中测试新型治疗方法的可能性来实现。探索新的治疗策略对于提高这些患者的生存率、保证良好的生活质量是必不可少的。

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Novel treatments for anaplastic thyroid carcinoma.间变性甲状腺癌的新型治疗方法。
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