Drilon A, Li G, Dogan S, Gounder M, Shen R, Arcila M, Wang L, Hyman D M, Hechtman J, Wei G, Cam N R, Christiansen J, Luo D, Maneval E C, Bauer T, Patel M, Liu S V, Ou S H I, Farago A, Shaw A, Shoemaker R F, Lim J, Hornby Z, Multani P, Ladanyi M, Berger M, Katabi N, Ghossein R, Ho A L
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York Department of Medicine, Weill Cornell Medical College, New York.
Ignyta, San Diego.
Ann Oncol. 2016 May;27(5):920-6. doi: 10.1093/annonc/mdw042. Epub 2016 Feb 15.
Mammary analogue secretory carcinoma (MASC) is a recently described pathologic entity. We report the case of a patient with an initial diagnosis of salivary acinic cell carcinoma later reclassified as MASC after next-generation sequencing revealed an ETV6-NTRK3 fusion.
This alteration was targeted with the pan-Trk inhibitor entrectinib (Ignyta), which possesses potent in vitro activity against cell lines containing various NTRK1/2/3 fusions.
A dramatic and durable response was achieved with entrectinib in this patient, followed by acquired resistance that correlated with the appearance of a novel NTRK3 G623R mutation. Structural modeling predicts that this alteration sterically interferes with drug binding, correlating to decreased sensitivity to drug inhibition observed in cell-based assays.
This first report of clinical activity with TrkC inhibition and the development of acquired resistance in an NTRK3-rearranged cancer emphasize the utility of comprehensive molecular profiling and targeted therapy for rare malignancies (NCT02097810).
乳腺样分泌性癌(MASC)是一种最近才被描述的病理实体。我们报告了一例最初诊断为唾液腺腺泡细胞癌的患者,在下一代测序显示ETV6-NTRK3融合后,该病例后来被重新分类为MASC。
这种改变用泛Trk抑制剂恩曲替尼(Ignyta)进行靶向治疗,恩曲替尼对含有各种NTRK1/2/3融合的细胞系具有强大的体外活性。
恩曲替尼在该患者中取得了显著且持久的反应,随后出现获得性耐药,这与一种新的NTRK3 G623R突变的出现相关。结构模型预测,这种改变在空间上干扰药物结合,这与在基于细胞的试验中观察到的对药物抑制的敏感性降低相关。
这篇关于TrkC抑制的临床活性以及NTRK3重排癌症中获得性耐药发展的首次报告强调了全面分子谱分析和靶向治疗对罕见恶性肿瘤的实用性(NCT02097810)。