Continuous response despite reduced dose of trametinib as single agent in an adolescent with a relapsed disseminated pediatric low-grade glioma KIAA1549-BRAF fusion positive: a case report and review of the literature

Serafin Castellano-Damaso, Felisa Vázquez-Gómez, Jose Luis Moreno-Carrasco, Begoña Arce, Pedro Borrego, Alvaro Lassaletta
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Abstract

Dissemination in pediatric low-grade glioma may occur in about 4%–10% of patients according to retrospective cohort studies. Due to its low incidence, there is no consensus on treatment for these patients. According to the constitutional activation of the MAPK/ERK pathway in these tumors, MEK inhibitors such as trametinib have been used successfully in the relapsed setting. Skin toxicity is frequent in patients receiving trametinib, normally mild to moderate, but sometimes severe, needing to discontinue the drug, limiting the efficacy in the tumor. There is not much information in the literature regarding whether reducing the dose of trametinib is able to maintain efficacy while, at the same time, decreasing toxicity. Here, we present an adolescent, with severe skin toxicity, whose trametinib dose was reduced by 50% and efficacy on the tumor continued while skin toxicity significantly decreased.
复发的播散性小儿低级别胶质瘤(KIAA1549-BRAF融合阳性)青少年在减少曲美替尼单药剂量后仍持续应答:病例报告和文献综述
根据回顾性队列研究,约有4%-10%的小儿低级别胶质瘤患者会发生扩散。由于发病率较低,对这些患者的治疗方法尚未达成共识。由于这些肿瘤中的MAPK/ERK通路被激活,MEK抑制剂(如曲美替尼)已被成功用于复发治疗。接受曲美替尼治疗的患者经常会出现皮肤毒性,通常为轻度至中度,但有时也会出现严重的皮肤毒性,需要停药,从而限制了对肿瘤的疗效。关于减少曲美替尼的剂量是否能在保持疗效的同时减少毒性,文献中的相关信息并不多。在此,我们介绍了一名患有严重皮肤毒性的青少年患者,在将曲美替尼的剂量减少50%后,其肿瘤疗效得以保持,而皮肤毒性则显著降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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