Wagle Nikhil, Grabiner Brian C, Van Allen Eliezer M, Amin-Mansour Ali, Taylor-Weiner Amaro, Rosenberg Mara, Gray Nathanael, Barletta Justine A, Guo Yanan, Swanson Scott J, Ruan Daniel T, Hanna Glenn J, Haddad Robert I, Getz Gad, Kwiatkowski David J, Carter Scott L, Sabatini David M, Jänne Pasi A, Garraway Levi A, Lorch Jochen H
From the Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School (N.W., E.M.V.A., N.G., R.I.H., D.J.K., P.A.J., L.A.G., J.H.L.), the Department of Medicine, Brigham and Women's Hospital and Harvard Medical School (N.W., E.M.V.A., Y.G., R.I.H., D.J.K., P.A.J., L.A.G., J.H.L.), the Departments of Pathology (J.A.B.) and Surgery (S.J.S., D.T.R.), Brigham and Women's Hospital, the Department of Medicine, Beth Israel Deaconess Medical Center (G.J.H.), and Belfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute (P.A.J.) - all in Boston; and Broad Institute of the Massachusetts Institute of Technology (MIT) and Harvard (N.W., E.M.V.A., A.A.-M., A.T.-W., M.R., G.G., D.J.K., S.L.C., D.M.S., L.A.G.), Whitehead Institute for Biomedical Research and the MIT Department of Biology (B.C.G., D.M.S.), and Howard Hughes Medical Institute, MIT (B.C.G., D.M.S.) - all in Cambridge, MA.
N Engl J Med. 2014 Oct 9;371(15):1426-33. doi: 10.1056/NEJMoa1403352.
Everolimus, an inhibitor of the mammalian target of rapamycin (mTOR), is effective in treating tumors harboring alterations in the mTOR pathway. Mechanisms of resistance to everolimus remain undefined. Resistance developed in a patient with metastatic anaplastic thyroid carcinoma after an extraordinary 18-month response. Whole-exome sequencing of pretreatment and drug-resistant tumors revealed a nonsense mutation in TSC2, a negative regulator of mTOR, suggesting a mechanism for exquisite sensitivity to everolimus. The resistant tumor also harbored a mutation in MTOR that confers resistance to allosteric mTOR inhibition. The mutation remains sensitive to mTOR kinase inhibitors.
依维莫司是一种雷帕霉素哺乳动物靶点(mTOR)抑制剂,对治疗mTOR通路发生改变的肿瘤有效。对依维莫司的耐药机制尚不清楚。一名转移性间变性甲状腺癌患者在获得长达18个月的显著缓解后出现了耐药。对治疗前和耐药肿瘤进行全外显子测序发现,mTOR的负调节因子TSC2存在无义突变,提示对依维莫司高度敏感的机制。耐药肿瘤的MTOR也存在一个突变,该突变赋予对变构mTOR抑制的耐药性。该突变对mTOR激酶抑制剂仍敏感。