Sarcomas More Common in Children
暂无分享,去创建一个
[1] Helen X. Chen,et al. Phase II study of cixutumumab in combination with temsirolimus in pediatric patients and young adults with recurrent or refractory sarcoma: A report from the children's oncology group , 2015, Pediatric blood & cancer.
[2] G. Demetri,et al. Phase II study of olaparib in patients with refractory Ewing sarcoma following failure of standard chemotherapy , 2014, BMC Cancer.
[3] J. Healey,et al. Ewing sarcoma in adults treated with modern radiotherapy techniques. , 2014, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.
[4] Jun S. Wei,et al. The Genomic Landscape of the Ewing Sarcoma Family of Tumors Reveals Recurrent STAG2 Mutation , 2014, PLoS genetics.
[5] M. Beckerle,et al. Reversible LSD1 Inhibition Interferes with Global EWS/ETS Transcriptional Activity and Impedes Ewing Sarcoma Tumor Growth , 2014, Clinical Cancer Research.
[6] G. Getz,et al. Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors. , 2014, Cancer discovery.
[7] W. Shi,et al. Adult rhabdomyosarcoma survival improved with treatment on multimodality protocols. , 2013, International journal of radiation oncology, biology, physics.
[8] C. Keller,et al. 18F‐FDG microPET imaging detects early transient response to an IGF1R inhibitor in genetically engineered rhabdomyosarcoma models , 2012, Pediatric blood & cancer.
[9] A. Llombart‐Bosch,et al. Lysine-specific demethylase 1 (LSD1/KDM1A/AOF2/BHC110) is expressed and is an epigenetic drug target in chondrosarcoma, Ewing's sarcoma, osteosarcoma, and rhabdomyosarcoma. , 2012, Human pathology.
[10] J. Desai,et al. Phase II study of ganitumab, a fully human anti-type-1 insulin-like growth factor receptor antibody, in patients with metastatic Ewing family tumors or desmoplastic small round cell tumors. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[11] Arul M Chinnaiyan,et al. PARP-1 inhibition as a targeted strategy to treat Ewing's sarcoma. , 2012, Cancer research.
[12] S. Ramaswamy,et al. Systematic identification of genomic markers of drug sensitivity in cancer cells , 2012, Nature.
[13] O. Delattre,et al. A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion , 2012, Nature Genetics.
[14] C. Antonescu,et al. High prevalence of CIC fusion with double‐homeobox (DUX4) transcription factors in EWSR1‐negative undifferentiated small blue round cell sarcomas , 2012, Genes, chromosomes & cancer.
[15] M. Zielenska,et al. The CIC-DUX4 fusion transcript is present in a subgroup of pediatric primitive round cell sarcomas. , 2012, Human pathology.
[16] Helen X. Chen,et al. Phase I/II trial and pharmacokinetic study of cixutumumab in pediatric patients with refractory solid tumors and Ewing sarcoma: a report from the Children's Oncology Group. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] U. Dirksen,et al. Preliminary efficacy of the anti-insulin-like growth factor type 1 receptor antibody figitumumab in patients with refractory Ewing sarcoma. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[18] D. Reinke,et al. R1507, a monoclonal antibody to the insulin-like growth factor 1 receptor, in patients with recurrent or refractory Ewing sarcoma family of tumors: results of a phase II Sarcoma Alliance for Research through Collaboration study. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[19] J. Neuhaus,et al. Clinical features and outcomes in patients with extraskeletal ewing sarcoma , 2011, Cancer.
[20] Qing-Rong Chen,et al. Identification of an inhibitor of the EWS-FLI1 oncogenic transcription factor by high-throughput screening. , 2011, Journal of the National Cancer Institute.
[21] James R. Anderson,et al. Results of the Intergroup Rhabdomyosarcoma Study Group D9602 protocol, using vincristine and dactinomycin with or without cyclophosphamide and radiation therapy, for newly diagnosed patients with low-risk embryonal rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Children's O , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[22] Yingye Zheng,et al. Genomic instability and copy‐number heterogeneity of chromosome 19q, including the kallikrein locus, in ovarian carcinomas , 2011, Molecular oncology.
[23] L. Helman,et al. Insulin-like growth factor 1 receptor antibody induces rhabdomyosarcoma cell death via a process involving AKT and Bcl-xL , 2010, Oncogene.
[24] C. Antonescu,et al. EWSR1‐POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty‐six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene , 2010, Genes, chromosomes & cancer.
[25] Daniel G. Miller,et al. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy , 2010, Science.
[26] G. L. de la Roza,et al. Newly described translocation (18;19)(q23;q13.2) in abdominal wall soft-tissue tumor resembling Ewing sarcoma/primitive neuroectodermal tumor. , 2010, Cancer genetics and cytogenetics.
[27] U. Dirksen,et al. Impact of EWS-ETS fusion type on disease progression in Ewing's sarcoma/peripheral primitive neuroectodermal tumor: prospective results from the cooperative Euro-E.W.I.N.G. 99 trial. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[28] J. Zell,et al. Analysis of prognostic factors in Ewing sarcoma using a population‐based cancer registry , 2010, Cancer.
[29] J. Neuhaus,et al. Ethnic and racial differences in patients with Ewing sarcoma , 2010, Cancer.
[30] S. Schuetze,et al. Safety, pharmacokinetics, and preliminary activity of the anti-IGF-1R antibody figitumumab (CP-751,871) in patients with sarcoma and Ewing's sarcoma: a phase 1 expansion cohort study. , 2010, The Lancet. Oncology.
[31] E. de Álava,et al. Desmoplastic nested spindle cell tumor of the liver in an adult. , 2010, Annals of diagnostic pathology.
[32] S. Wolden,et al. Sarcomas across the age spectrum. , 2010, Seminars in radiation oncology.
[33] A. Tolcher,et al. Phase I, pharmacokinetic, and pharmacodynamic study of AMG 479, a fully human monoclonal antibody to insulin-like growth factor receptor 1. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[34] M. Shago,et al. Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC-DUX4 fusion gene event. , 2009, Cancer genetics and cytogenetics.
[35] A. Rosato,et al. Undifferentiated sarcoma: does it exist? A clinicopathologic study of 7 pediatric cases and review of literature. , 2009, Human pathology.
[36] F. Pedeutour,et al. Fusion of EWSR1 with the DUX4 facioscapulohumeral muscular dystrophy region resulting from t(4;22)(q35;q12) in a case of embryonal rhabdomyosarcoma. , 2009, Cancer genetics and cytogenetics.
[37] James R. Anderson,et al. Vincristine, actinomycin, and cyclophosphamide compared with vincristine, actinomycin, and cyclophosphamide alternating with vincristine, topotecan, and cyclophosphamide for intermediate-risk rhabdomyosarcoma: children's oncology group study D9803. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[38] Paul A Meyers,et al. Phase II multicenter trial of imatinib in 10 histologic subtypes of sarcoma using a bayesian hierarchical statistical model. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[39] H. Makhlouf,et al. Calcifying Nested Stromal-epithelial Tumors of the Liver: A Clinicopathologic, Immunohistochemical, and Molecular Genetic Study of 9 Cases With a Long-term Follow-up , 2009, The American journal of surgical pathology.
[40] A. Hayes-Jordan,et al. Rhabdomyosarcoma in children , 2009, Current opinion in pediatrics.
[41] P. Leavey,et al. Dose-intensified compared with standard chemotherapy for nonmetastatic Ewing sarcoma family of tumors: a Children's Oncology Group Study. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[42] J. Crowley,et al. A SARC global collaborative phase II trial of R1507, a recombinant human monoclonal antibody to the insulin-like growth factor-1 receptor (IGF1R) in patients with recurrent or refractory sarcomas. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[43] S. de Jong,et al. The insulin‐like growth factor system and sarcomas , 2009, The Journal of pathology.
[44] P. Sorensen,et al. Molecular classification of rhabdomyosarcoma--genotypic and phenotypic determinants of diagnosis: a report from the Children's Oncology Group. , 2009, The American journal of pathology.
[45] Xia Han,et al. The mechanisms of differential sensitivity to an insulin-like growth factor-1 receptor inhibitor (BMS-536924) and rationale for combining with EGFR/HER2 inhibitors. , 2009, Cancer research.
[46] L. Helman,et al. Addiction to elevated insulin-like growth factor I receptor and initial modulation of the AKT pathway define the responsiveness of rhabdomyosarcoma to the targeting antibody. , 2008, Cancer research.
[47] W. Winkelmann,et al. Results of the EICESS-92 Study: two randomized trials of Ewing's sarcoma treatment--cyclophosphamide compared with ifosfamide in standard-risk patients and assessment of benefit of etoposide added to standard treatment in high-risk patients. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[48] D. West,et al. Randomized comparison of every-two-week v. every-three-week chemotherapy in Ewing sarcoma family tumors (ESFT) , 2008 .
[49] D. Rakheja,et al. Translocation (4;19)(q35;q13.1)–Associated Primitive round Cell Sarcoma: Report of a Case and Review of the Literature , 2008, Pediatric and Developmental Pathology.
[50] D. Hawkins,et al. Two boys with fragile x syndrome and hepatic tumors. , 2008, Journal of pediatric hematology/oncology.
[51] U. Surti,et al. EWSR1‐CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma , 2007, Genes, chromosomes & cancer.
[52] Soma Das,et al. Phase II trial of irinotecan in children with refractory solid tumors: a Children's Oncology Group Study. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[53] J. Codina,et al. Molecular biology of rhabdomyosarcoma , 2007 .
[54] P. Thall,et al. Randomized phase II study of gemcitabine and docetaxel compared with gemcitabine alone in patients with metastatic soft tissue sarcomas: results of sarcoma alliance for research through collaboration study 002 [corrected]. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[55] K. S. Hall,et al. Non-metastatic Ewing's family tumors: High-dose chemotherapy with stem cell rescue in poor responder patients. Preliminary results of the Italian/Scandinavian ISG/SSG III protocol , 2007 .
[56] L. Helman,et al. Rapamycin induces feedback activation of Akt signaling through an IGF-1R-dependent mechanism , 2007, Oncogene.
[57] S. Spunt,et al. Distinguishing Undifferentiated Embryonal Sarcoma of the Liver from Biliary Tract Rhabdomyosarcoma: A Children's Oncology Group Study , 2007, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
[58] P. Houghton,et al. Two consecutive phase II window trials of irinotecan alone or in combination with vincristine for the treatment of metastatic rhabdomyosarcoma: the Children's Oncology Group. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[59] M Beth McCarville,et al. Temozolomide and intravenous irinotecan for treatment of advanced Ewing sarcoma , 2007, Pediatric blood & cancer.
[60] B. Geoerger,et al. Phase II trial of irinotecan in children with relapsed or refractory rhabdomyosarcoma: a joint study of the French Society of Pediatric Oncology and the United Kingdom Children's Cancer Study Group. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[61] A. McTiernan,et al. Improving Outcomes After Relapse in Ewing's Sarcoma: Analysis of 114 Patients From a Single Institution , 2006, Sarcoma.
[62] J. Ewing. The Classic: Diffuse endothelioma of bone. Proceedings of the New York Pathological Society. 1921;12:17. , 2006, Clinical orthopaedics and related research.
[63] P. Terrier,et al. Impact of high-dose busulfan plus melphalan as consolidation in metastatic Ewing tumors: a study by the Société Française des Cancers de l'Enfant. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[64] J. Boos,et al. Phase II study of gemcitabine in children with solid tumors of mesenchymal and embryonic origin , 2006, Anti-cancer drugs.
[65] James R. Anderson,et al. Pooled analysis of phase II window studies in children with contemporary high-risk metastatic rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[66] H. Aburatani,et al. Fusion between CIC and DUX4 up-regulates PEA3 family genes in Ewing-like sarcomas with t(4;19)(q35;q13) translocation. , 2006, Human molecular genetics.
[67] H. Kovar,et al. Ewing's sarcoma family of tumors: current management. , 2006, The oncologist.
[68] M. Carli,et al. Phase II study of a protracted irinotecan schedule in children with refractory or recurrent soft tissue sarcoma , 2006, Cancer.
[69] 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.
[70] K. Anderson,et al. Desmoplastic Nested Spindle Cell Tumor of Liver: Report of Four Cases of a Proposed New Entity , 2005, The American journal of surgical pathology.
[71] W. Meyer,et al. Efficacy of topotecan and cyclophosphamide given in a phase II window trial in children with newly diagnosed metastatic rhabdomyosarcoma: a Children's Oncology Group study. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[72] A. McTiernan,et al. Single center experience of a new intensive induction therapy for ewing's family of tumors: feasibility, toxicity, and stem cell mobilization properties. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[73] S. Donaldson,et al. Addition of ifosfamide and etoposide to standard chemotherapy for Ewing's sarcoma and primitive neuroectodermal tumor of bone. , 2003, The New England journal of medicine.
[74] Sung-Eun Jung,et al. Undifferentiated (embryonal) sarcoma of the liver: combination treatment by surgery and chemotherapy. , 2002, Journal of pediatric surgery.
[75] W. Gerald,et al. Irinotecan for Pediatric Solid Tumors: The Memorial Sloan-Kettering Experience , 2002, Journal of pediatric hematology/oncology.
[76] M. Bernstein,et al. Cyclophosphamide plus topotecan in children with recurrent or refractory solid tumors: a Pediatric Oncology Group phase II study. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[77] James R. Anderson,et al. Intergroup rhabdomyosarcoma study-IV: results for patients with nonmetastatic disease. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[78] 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.
[79] P. Meyers,et al. How effective is dose-intensive/myeloablative therapy against Ewing's sarcoma/primitive neuroectodermal tumor metastatic to bone or bone marrow? The Memorial Sloan-Kettering experience and a literature review. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[80] J. Meza,et al. Up-front window trial of topotecan in previously untreated children and adolescents with metastatic rhabdomyosarcoma: an intergroup rhabdomyosarcoma study. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[81] C. Croce,et al. Exon structure and promoter identification of STIM1 (alias GOK), a human gene causing growth arrest of the human tumor cell lines G401 and RD , 1999, Cytogenetic and Genome Research.
[82] M. Bernstein,et al. Topotecan in Pediatric Patients With Recurrent and Progressive Solid Tumors: A Pediatric Oncology Group Phase II Study , 1998, Journal of pediatric hematology/oncology.
[83] D. Leroith,et al. Expression of a kinase‐deficient IGF‐I‐R suppresses tumorigenicity of rhabdomyosarcoma cells constitutively expressing a wild type IGF‐I‐R , 1998, International Journal of Cancer.
[84] 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.
[85] C. Stewart,et al. Phase I study of topotecan in combination with cyclophosphamide in pediatric patients with malignant solid tumors: a Pediatric Oncology Group Study. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[86] P. Adamson,et al. Phase II trial of topotecan administered as 72-hour continuous infusion in children with refractory solid tumors: a collaborative Pediatric Branch, National Cancer Institute, and Children's Cancer Group Study. , 1998, Clinical cancer research : an official journal of the American Association for Cancer Research.
[87] A. Feinberg,et al. A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes. , 1997, Genomics.
[88] C. Croce,et al. GOK: a gene at 11p15 involved in rhabdomyosarcoma and rhabdoid tumor development. , 1997, Cancer research.
[89] J. Finklestein,et al. t(4;19)(q35;q13.1): a recurrent change in primitive mesenchymal tumors? , 1995, Cancer genetics and cytogenetics.
[90] H. Werner,et al. The Role of the Insulin‐like Growth Factor‐I Receptor in Cancer , 1995, Annals of the New York Academy of Sciences.
[91] E. Gehan,et al. The Third Intergroup Rhabdomyosarcoma Study. , 1995, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[92] Chuan Yi Tang,et al. A 2.|E|-Bit Distributed Algorithm for the Directed Euler Trail Problem , 1993, Inf. Process. Lett..
[93] E. Gehan,et al. The intergroup rhabdomyosarcoma study‐II , 1993, Cancer.
[94] L. Helman,et al. IGF-II in the pathogenesis of rhabdomyosarcoma: a prototype of IGFs involvement in human tumorigenesis. , 1993, Advances in Experimental Medicine and Biology.
[95] I. Lewis,et al. 12q13 abnormality in rhabdomyosarcoma. A nonrandom occurrence? , 1992, Cancer genetics and cytogenetics.
[96] J. Biegel,et al. Chromosomal Translocation t(1;13)(p36;q14) in a Case of Rhabdomyosarcoma , 1991, Genes, chromosomes & cancer.
[97] E. Gehan,et al. Multimodal therapy for the management of primary, nonmetastatic Ewing's sarcoma of bone: a long-term follow-up of the First Intergroup study. , 1990, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[98] E. Gehan,et al. Multimodal therapy for the management of nonpelvic, localized Ewing's sarcoma of bone: intergroup study IESS-II. , 1990, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[99] E. Gehan,et al. The intergroup rhabdomyosarcoma study‐I. A final report , 1988, Cancer.
[100] H. Shimada,et al. Histopathology of childhood sarcomas, Intergroup Rhabdomyosarcoma Studies I and II: clinicopathologic correlation. , 1988, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[101] P. Houghton,et al. A specific chromosomal abnormality in rhabdomyosarcoma. , 1987, Cytogenetics and cell genetics.
[102] M. Beltangady,et al. Infants younger than 1 year of age with rhabdomyosarcoma , 1986, Cancer.
[103] M. Tattersall,et al. Extraskeletal Ewing's sarcoma: a clinical, morphological and ultrastructural analysis of five cases with a review of the literature. , 1986, European journal of cancer & clinical oncology.
[104] C. Turc‐Carel,et al. Consistent chromosomal translocation in alveolar rhabdomyosarcoma. , 1986, Cancer genetics and cytogenetics.
[105] G. Rosen,et al. Mesenchymal chondrosarcoma a clinicopathologic analysis of 35 patients with emphasis on treatment , 1983, Cancer.
[106] H. Maurer. The Intergroup Rhabdomyosarcoma Study II: objectives and study design. , 1980, Journal of pediatric surgery.
[107] K. Ishak,et al. Undifferentiated (embryonal) sarcoma of the liver. Report of 31 cases , 1978, Cancer.
[108] L. Norton,et al. Tumor size, sensitivity to therapy, and design of treatment schedules. , 1977, Cancer treatment reports.
[109] L. Norton,et al. Predicting the course of Gompertzian growth , 1976, Nature.
[110] Oldham Rk,et al. Treatment of Ewing's sarcoma with adriamycin (NSC-123127). , 1972 .
[111] J. Ewing. Diffuse endothelioma of bone , 1972 .
[112] H. G. Taylor,et al. Prognosis in childhood rhabdomyosarcoma , 1970, Cancer.
[113] Sutow Ww,et al. Successful chemotherapy for childhood rhabdomyosarcoma. , 1970 .
[114] M. Haggard,et al. CYCLOPHOSPHAMIDE (NSC-26271)-1 IN UNCOMMON MALIGNANT NEOPLASMS IN CHILDREN. , 1964, Cancer chemotherapy reports.
[115] D. Dahlin,et al. Mesenchymal chondrosarcoma. Further observations on a new entity , 1962, Cancer.