What Do We Know about Survival in Skeletally Premature Children Aged 0 to 10 Years with Ewing Sarcoma? A Multicenter 10-Year Follow-Up Study in 60 Patients
暂无分享,去创建一个
L. Sierrasesúmaga | M. A. van de Sande | M. San-Julián | L. van der Heijden | M. A. van de Sande | L. Haveman | H. Merks | S. Bosma | L. Sierrasesúmaga
[1] M. San-Julián,et al. A Reassessment of the Barrier Effect of the Physis against Metaphyseal Osteosarcoma: A Comprehensive Pathological Study with Its Radiological and Clinical Follow-Up Correlations , 2022, Diagnostics.
[2] C. Rodríguez-Galindo,et al. Subsequent Malignant Neoplasm of Bone in Children and Adolescent—Possibility of Multimodal Treatment , 2022, Current oncology.
[3] S. Sleijfer,et al. Bone sarcomas: ESMO-EURACAN-GENTURIS-ERNPaedCan Clinical Practice Guideline for diagnosis, treatment and follow-up. , 2021, Annals of oncology : official journal of the European Society for Medical Oncology.
[4] G. Farfalli,et al. Biology and technology in the surgical treatment of malignant bone tumours in children and adolescents, with a special note on the very young , 2021, Journal of children's orthopaedics.
[5] S. DuBois,et al. Second malignancies in patients treated for Ewing sarcoma: A systematic review , 2019, Pediatric blood & cancer.
[6] G. Armstrong,et al. Chemotherapy and Risk of Subsequent Malignant Neoplasms in the Childhood Cancer Survivor Study Cohort. , 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[7] J. Carr,et al. Registry , 2019, Definitions.
[8] H. Gelderblom,et al. Prognostic factors for survival in Ewing sarcoma: A systematic review. , 2018, Surgical oncology.
[9] P. Dartevelle,et al. Ewing Sarcoma of the Chest Wall: Prognostic Factors of Multimodal Therapy Including En Bloc Resection. , 2018, The Annals of thoracic surgery.
[10] A. Puri,et al. Reconstructing diaphyseal tumors using radiated (50 Gy) autogenous tumor bone graft , 2018, Journal of surgical oncology.
[11] U. Dirksen,et al. Age dependency of primary tumor sites and metastases in patients with Ewing sarcoma , 2018, Pediatric blood & cancer.
[12] U. Dirksen,et al. Rhabdomyosarcoma, Ewing Sarcoma, and Other Round Cell Sarcomas. , 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[13] Yubo Gao,et al. Does surgery or radiation provide the best overall survival in Ewing's sarcoma? A review of the National Cancer Data Base , 2017, Journal of surgical oncology.
[14] Chi Lin,et al. A Comparison of Pediatric vs. Adult Patients with the Ewing Sarcoma Family of Tumors , 2017, Front. Oncol..
[15] M. McAleer,et al. Ewing sarcoma family of tumors in children younger than 10 years of age , 2017, Pediatric blood & cancer.
[16] R. Grimer,et al. Ewing's sarcoma: only patients with 100% of necrosis after chemotherapy should be classified as having a good response. , 2016, The bone & joint journal.
[17] U. Dirksen,et al. Can postoperative radiotherapy be omitted in localised standard-risk Ewing sarcoma? An observational study of the Euro-E.W.I.N.G group. , 2016, European journal of cancer.
[18] R. Randall,et al. Age, Tumor Characteristics, and Treatment Regimen as Event Predictors in Ewing: A Children's Oncology Group Report , 2015, Sarcoma.
[19] 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.
[20] U. Dirksen,et al. Local Control in Ewing Sarcoma of the Chest Wall: Results of the EURO-EWING 99 Trial , 2015, Annals of Surgical Oncology.
[21] M. Sharma,et al. Developing a prognostic model for localized Ewing sarcoma family of tumors: A single institutional experience of 224 cases treated with uniform chemotherapy protocol , 2015, Journal of surgical oncology.
[22] R. Cozza,et al. Ewing Sarcoma of the Bone in Children under 6 Years of Age , 2013, PloS one.
[23] A. McTiernan,et al. Incidence and survival of malignant bone sarcomas in England 1979–2007 , 2012, International journal of cancer.
[24] B. Bui,et al. Risk adapted chemotherapy for localised Ewing's sarcoma of bone: the French EW93 study. , 2012, European journal of cancer.
[25] M. Geraci,et al. The contrasting age‐incidence patterns of bone tumours in teenagers and young adults: Implications for aetiology , 2011, International journal of cancer.
[26] K. Ness,et al. Long-term survivors of childhood Ewing sarcoma: report from the childhood cancer survivor study. , 2010, Journal of the National Cancer Institute.
[27] U. Dirksen,et al. Primary disseminated multifocal Ewing sarcoma: results of the Euro-EWING 99 trial. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[28] S. Hopyan,et al. Clinical outcome of children and adults with localized Ewing sarcoma , 2010, Cancer.
[29] J. Zell,et al. Analysis of prognostic factors in Ewing sarcoma using a population‐based cancer registry , 2010, Cancer.
[30] L. Koniaris,et al. Ewing sarcoma demonstrates racial disparities in incidence‐related and sex‐related differences in outcome , 2009, Cancer.
[31] D. Lefkopoulos,et al. Risk of a second malignant neoplasm after cancer in childhood treated with radiotherapy: correlation with the integral dose restricted to the irradiated fields. , 2008, International journal of radiation oncology, biology, physics.
[32] P. Hogendoorn,et al. Incidence of Biopsy-Proven Bone Tumors in Children: A Report Based on the Dutch Pathology Registration "PALGA" , 2008, Journal of pediatric orthopedics.
[33] R. Curtis,et al. New malignancies following childhood cancer in the United States, 1973–2002 , 2007, International journal of cancer.
[34] E. Steliarova-Foucher,et al. Bone tumours in European children and adolescents, 1978-1997. Report from the Automated Childhood Cancer Information System project. , 2006, European journal of cancer.
[35] E. Steliarova-Foucher,et al. Cancer incidence and survival in European adolescents (1978-1997). Report from the Automated Childhood Cancer Information System project. , 2006, European journal of cancer.
[36] P. Picci,et al. The role of surgical margins in treatment of Ewing's sarcoma family tumors: experience of a single institution with 512 patients treated with adjuvant and neoadjuvant chemotherapy. , 2006, International journal of radiation oncology, biology, physics.
[37] M. Koshy,et al. Radiation-induced osteosarcomas in the pediatric population. , 2005, International journal of radiation oncology, biology, physics.
[38] R. Reid,et al. Ewing's Sarcoma of the Upper Extremity: Presenting Symptoms, Diagnostic Delay and Outcome , 2005, Sarcoma.
[39] F. Sim,et al. Ewing’s Sarcoma and the Development of Secondary Malignancies , 2003, Clinical orthopaedics and related research.
[40] 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.
[41] H. Hense,et al. Factors associated with tumor volume and primary metastases in Ewing tumors: results from the (EI)CESS studies. , 1999, Annals of oncology : official journal of the European Society for Medical Oncology.
[42] J. Blay,et al. Ewing's family of tumors in adults: multivariate analysis of survival and long-term results of multimodality therapy in 182 patients. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[43] S. Ferrari,et al. Long-term follow-up for patients with Ewing's sarcoma of bone treated with adjuvant and neoadjuvant chemotherapy. , 1997, Oncology reports.
[44] D. Fairclough,et al. Second malignancies after Ewing's sarcoma: radiation dose-dependency of secondary sarcomas. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[45] H. Roels,et al. Limb conservation in primary bone tumours by resection, extracorporeal irradiation and re-implantation. , 1988, The Journal of bone and joint surgery. British volume.
[46] 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.
[47] C. Fletcher,et al. WHO classification of tumours of soft tissue and bone , 2013 .
[48] 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 .
[49] E. Pignotti,et al. Long-term outcome for patients with non-metastatic Ewing's sarcoma treated with adjuvant and neoadjuvant chemotherapies. 402 patients treated at Rizzoli between 1972 and 1992. , 2004, European journal of cancer.
[50] H. Jürgens,et al. Prognostic significance of tumor volume in localized Ewing's sarcoma of bone in children and adolescents , 2004, Journal of Cancer Research and Clinical Oncology.
[51] W. Winkelmann,et al. Local therapy in localized Ewing tumors: results of 1058 patients treated in the CESS 81, CESS 86, and EICESS 92 trials. , 2003, International journal of radiation oncology, biology, physics.
[52] L. Sunde,et al. Ewing's sarcoma. A retrospective study of prognostic factors and treatment results. , 1987, Acta oncologica.
[53] O. Sneppen,et al. Presenting symptoms and treatment delay in osteosarcoma and Ewing's sarcoma. , 1984, Acta radiologica. Oncology.