Lynch syndrome-associated chordoma with high tumor mutational burden and significant response to immune checkpoint inhibitors
暂无分享,去创建一个
N. Shinojima | A. Mukasa | Takahiro Yamamoto | Y. Tomita | H. Matsui | Y. Komohara | Kazutaka Ozono | Ken Uekawa | K. Nosaka | Hiroaki Matsuzaki | Haruaki Yamamoto | Azusa Kai | Rumi Sasaki | Yoshiki Mikami | Sakiko Abe | Ryosuke Mori
[1] S. Gui,et al. Mid-term follow-up surgical results in 284 cases of clival chordomas: the risk factors for outcome and tumor recurrence , 2021, Neurosurgical Review.
[2] Michael Lim,et al. Immunotherapy for Chordoma and Chondrosarcoma: Current Evidence , 2021, Cancers.
[3] X. Hua,et al. Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival , 2021, Nature Communications.
[4] K. Yamaguchi,et al. Role of Tumor Mutation Burden Analysis in Detecting Lynch Syndrome in Precision Medicine: Analysis of 2,501 Japanese Cancer Patients , 2020, Cancer Epidemiology, Biomarkers & Prevention.
[5] Y. Bang,et al. Association of tumour mutational burden with outcomes in patients with advanced solid tumours treated with pembrolizumab: prospective biomarker analysis of the multicohort, open-label, phase 2 KEYNOTE-158 study. , 2020, The Lancet. Oncology.
[6] J. Barnholtz-Sloan,et al. Descriptive epidemiology of chordomas in the United States , 2020, Journal of Neuro-Oncology.
[7] F. Soylemezoğlu,et al. Poorly differentiated chordoma: review of 53 cases , 2019, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.
[8] Jianying Zhou,et al. Pembrolizumab versus chemotherapy for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer (KEYNOTE-042): a randomised, open-label, controlled, phase 3 trial , 2019, The Lancet.
[9] J. Lunceford,et al. Pan-tumor genomic biomarkers for PD-1 checkpoint blockade–based immunotherapy , 2018, Science.
[10] G. Nielsen,et al. Clinicopathologic characteristics of poorly differentiated chordoma , 2018, Modern Pathology.
[11] Ahmet Zehir,et al. Molecular Determinants of Response to Anti-Programmed Cell Death (PD)-1 and Anti-Programmed Death-Ligand 1 (PD-L1) Blockade in Patients With Non-Small-Cell Lung Cancer Profiled With Targeted Next-Generation Sequencing. , 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[12] B. Landis,et al. First report of clinical responses to immunotherapy in 3 relapsing cases of chordoma after failure of standard therapies , 2017, Oncoimmunology.
[13] Levi Garraway,et al. Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden , 2017, Genome Medicine.
[14] M. Irie. Brain Tumor Registry of Japan (2005–2008) , 2017, Neurologia medico-chirurgica.
[15] K. Schaller,et al. Incidence and relative survival of chordomas , 2013, Cancer.
[16] H. Vasen. Review article: the Lynch syndrome (hereditary nonpolyposis colorectal cancer) * , 2007, Alimentary pharmacology & therapeutics.
[17] A. Samii,et al. Chordomas of the skull base: surgical management and outcome. , 2007, Journal of neurosurgery.
[18] W. Weber,et al. Case Report: Familial Gastric Cancer and Chordoma in the Same Family , 2005, Hereditary Cancer in Clinical Practice.