Risk stratification by somatic mutation burden in Ewing sarcoma
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Andrzej Niemierko | Nayan Lamba | A. Niemierko | D. Haas-Kogan | S. DuBois | N. Lamba | Kevin X. Liu | William L. Hwang | Steven G. DuBois | Daphne A. Haas‐Kogan | Kevin X. Liu | William L. Hwang
[1] M. Mann,et al. A review of soft-tissue sarcomas: translation of biological advances into treatment measures , 2018, Cancer management and research.
[2] D. Compton,et al. STAG2 promotes error correction in mitosis by regulating kinetochore–microtubule attachments , 2014, Journal of Cell Science.
[3] W. Winkelmann,et al. Localized Ewing tumor of bone: final results of the cooperative Ewing's Sarcoma Study CESS 86. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[4] U. Moll,et al. Links between mutant p53 and genomic instability , 2012, Journal of cellular biochemistry.
[5] A. Craft,et al. Prognostic factors in Ewing's tumor of bone: analysis of 975 patients from the European Intergroup Cooperative Ewing's Sarcoma Study Group. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[6] C. Beauchamp. Ewing Sarcoma Demonstrates Racial Disparities in Incidence-related and Sex-related Differences in Outcome: An Analysis of 1631 Cases From the SEER Database, 1973-2005 , 2010 .
[7] A. McKenna,et al. The genomic landscape of pediatric Ewing sarcoma. , 2014, Cancer discovery.
[8] Shamil R. Sunyaev,et al. Impact of deleterious passenger mutations on cancer progression , 2012, Proceedings of the National Academy of Sciences.
[9] K. Cole,et al. Comprehensive Analysis of Hypermutation in Human Cancer , 2017, Cell.
[10] T. Halazonetis,et al. Genomic instability — an evolving hallmark of cancer , 2010, Nature Reviews Molecular Cell Biology.
[11] Nikhil Wagle,et al. High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. , 2012, Cancer discovery.
[12] Benjamin E. Gross,et al. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. , 2012, Cancer discovery.
[13] A. Niemierko,et al. Clinical Impact of Tumor Mutational Burden in Neuroblastoma. , 2018, Journal of the National Cancer Institute.
[14] S. Ferrari,et al. Prognostic factors in non-metastatic Ewing's sarcoma tumor of bone: An analysis of 579 patients treated at a single institution with adjuvant or neoadjuvant chemotherapy between 1972 and 1998 , 2006, Acta oncologica.
[15] Benjamin E. Gross,et al. Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal , 2013, Science Signaling.
[16] I. Judson,et al. How to treat the Ewing's family of sarcomas in adult patients. , 2006, The oncologist.
[17] L. Koniaris,et al. Ewing sarcoma demonstrates racial disparities in incidence‐related and sex‐related differences in outcome , 2009, Cancer.
[18] U. Dirksen,et al. Ewing Sarcoma: Current Management and Future Approaches Through Collaboration. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[19] J. Healey,et al. Randomized controlled trial of interval-compressed chemotherapy for the treatment of localized Ewing sarcoma: a report from the Children's Oncology Group. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] W. Gerald,et al. EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[21] Jun S. Wei,et al. The Genomic Landscape of the Ewing Sarcoma Family of Tumors Reveals Recurrent STAG2 Mutation , 2014, PLoS genetics.
[22] M. Ladanyi,et al. Ewing sarcomas with p53 mutation or p16/p14ARF homozygous deletion: a highly lethal subset associated with poor chemoresponse. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[23] Michael C. Heinold,et al. The landscape of genomic alterations across childhood cancers , 2018, Nature.
[24] Yubo Gao,et al. Prognostic factors for survival in patients with Ewing's sarcoma using the surveillance, epidemiology, and end results (SEER) program database. , 2015, Cancer epidemiology.
[25] Li Ding,et al. Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. , 2014, Cancer discovery.
[26] A. Llombart‐Bosch,et al. Molecular Analysis of the 9p21 Locus and p53 Genes in Ewing Family Tumors , 2001, Laboratory Investigation.