SELNET Clinical practice guidelines for bone sarcoma.
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R. Maki | A. D. Dei Tos | J. Martín-Broto | S. Stacchiotti | C. Valverde | K. Scotlandi | A. Frezza | B. Kasper | J. Blay | P. Collini | D. Donati | E. Palmerini | A. Righi | S. Casavilca-Zambrano | M. Karanian | A. Lopes | F. Gouin | D. Moura | N. Hindi | A. Nascimento | T. Frisoni | A. López-pousa | J. Martínez-Tláhuel | H. Martínez-Said | S. Provenzano | M. Eriksson | F. Waisberg | M. Angel | D. Bernabeu | D. García-Ortega | M. Clara-Altamirano | C. Mello | E. Ortiz-Cruz | M. Gómez-Mateo | A. Gronchi | S. Nakagawa | F. D. Costa | J. Bollard | M. Chacon | T. Soulé | S. Aguiar | B. Araya | R. Badilla | F. Campos | Caro-Sánchez Chs | A. Carvajal Montoya | Castro-Oliden | R. Correa Genoroso | M. Cuellar | H. Domínguez Malagón | A. Dufresne | M. Farias-Loza | H. Gerderblom | J. Haro | L. Huanca | N. Jiménez | B. B. Lopes David | G. Lutter | J. M. Morales Pérez | S. Patel | Y. Pfluger | A. Rodríguez | T. Santos | Silva Mlg | E. Zamora Estrada | J. Morales Pérez | F. Waisberg | JY Blay | A.P. Dei Tos | M.A. Clara-Altamirano | FD Costa | HR Dominguez Malagon | DM Donati | A. Frezza | D.Y. Garcia-Ortega | MC Gómez-Mateo | B. L. Lopes David | RG Maki | JL Martínez-Tlahuel | CA Mello | DS Moura | SA Nakagawa | AG Nascimento | EJ Ortiz-Cruz | TG Santos | CM Valverde | A. Dei Tos | M. Clara-Altamirano | D. Garcia-Ortega | D.S. Moura | C. Valverde | R. Maki
[1] J. Blay,et al. Malignancy in giant cell tumor of bone: analysis of an open-label phase 2 study of denosumab , 2021, BMC Cancer.
[2] D. Vanel,et al. High Dose Ifosfamide in Relapsed and Unresectable High-Grade Osteosarcoma Patients: A Retrospective Series , 2020, Cells.
[3] E. Staals,et al. Rare Primary Malignant Bone Sarcomas , 2020, Cancers.
[4] H. Gelderblom,et al. Current concepts in the treatment of giant cell tumour of bone. , 2020, Current opinion in oncology.
[5] U. Dirksen,et al. Results of the second interim assessment of rEECur, an international randomized controlled trial of chemotherapy for the treatment of recurrent and primary refractory Ewing sarcoma (RR-ES). , 2020, Journal of Clinical Oncology.
[6] H. Gelderblom,et al. Comparison of two chemotherapy regimens in Ewing sarcoma (ES): Overall and subgroup results of the Euro Ewing 2012 randomized trial (EE2012). , 2020 .
[7] L. Spector,et al. Prognostic Factors for Development of Subsequent Metastases in Localized Osteosarcoma: A Systematic Review and Identification of Literature Gaps , 2020, Sarcoma.
[8] P. Gikas,et al. The sensitivity, specificity, and diagnostic accuracy of whole-bone MRI for identifying skip metastases in appendicular osteosarcoma and Ewing sarcoma , 2020, Skeletal Radiology.
[9] P. Rose. What's New in Musculoskeletal Tumor Surgery. , 2019, The Journal of bone and joint surgery. American volume.
[10] J. Blay,et al. Denosumab in patients with giant-cell tumour of bone: a multicentre, open-label, phase 2 study. , 2019, The Lancet. Oncology.
[11] S. Millis,et al. Clinical, pathological, and genomic features of EWSR1-PATZ1 fusion sarcoma , 2019, Modern Pathology.
[12] J. Blay,et al. Surgery in reference centers improves survival of sarcoma patients: a nationwide study , 2019, Annals of oncology : official journal of the European Society for Medical Oncology.
[13] S. Ferrari,et al. Bone marrow biopsy in the initial staging of Ewing sarcoma: Experience from a single institution , 2019, Pediatric blood & cancer.
[14] K. S. Hall,et al. Results of the first interim assessment of rEECur, an international randomized controlled trial of chemotherapy for the treatment of recurrent and primary refractory Ewing sarcoma. , 2019, Journal of Clinical Oncology.
[15] J. Blay,et al. Efficacy and safety of regorafenib in adult patients with metastatic osteosarcoma: a non-comparative, randomised, double-blind, placebo-controlled, phase 2 study. , 2019, The Lancet. Oncology.
[16] S. Sleijfer,et al. Bone sarcomas: ESMO-PaedCan-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up. , 2018 .
[17] J. Blay,et al. High-Dose Chemotherapy and Blood Autologous Stem-Cell Rescue Compared With Standard Chemotherapy in Localized High-Risk Ewing Sarcoma: Results of Euro-E.W.I.N.G.99 and Ewing-2008. , 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[18] D. Campanacci,et al. Denosumab treatment of inoperable or locally advanced giant cell tumor of bone - Multicenter analysis outside clinical trial. , 2018, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.
[19] J. Whelan,et al. Osteosarcoma, Chondrosarcoma, and Chordoma. , 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] C. Antonescu,et al. BCOR-CCNB3 Fusion Positive Sarcomas: A Clinicopathologic and Molecular Analysis of 36 Cases With Comparison to Morphologic Spectrum and Clinical Behavior of Other Round Cell Sarcomas , 2017, The American journal of surgical pathology.
[21] S. Bielack,et al. EURO-B.O.S.S.: A European study on chemotherapy in bone-sarcoma patients aged over 40: Outcome in primary high-grade osteosarcoma , 2018, Tumori.
[22] L. Tang,et al. Efficacy and safety of stereotactic radiosurgery for pulmonary metastases from osteosarcoma: Experience in 73 patients , 2017, Scientific Reports.
[23] J. Blay,et al. Improved survival using specialized multidisciplinary board in sarcoma patients. , 2017 .
[24] F. Moreno,et al. Childhood osteosarcoma: Incidence and survival in Argentina. Report from the National Pediatric Cancer Registry, ROHA Network 2000–2013 , 2017, Pediatric blood & cancer.
[25] H. Peng,et al. Is intralesional resection suitable for central grade 1 chondrosarcoma: A systematic review and updated meta-analysis. , 2017, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.
[26] C. Antonescu,et al. Sarcomas With CIC-rearrangements Are a Distinct Pathologic Entity With Aggressive Outcome: A Clinicopathologic and Molecular Study of 115 Cases , 2017, The American journal of surgical pathology.
[27] J. Blay,et al. Advanced chordoma treated by first-line molecular targeted therapies: Outcomes and prognostic factors. A retrospective study of the French Sarcoma Group (GSF/GETO) and the Association des Neuro-Oncologues d'Expression Française (ANOCEF). , 2017, European Journal of Cancer.
[28] J. Blay,et al. Giant cell tumour of bone in the denosumab era. , 2017, European journal of cancer.
[29] P. A. Gardner,et al. Best practices for the management of local-regional recurrent chordoma: a position paper by the Chordoma Global Consensus Group , 2017, Annals of oncology : official journal of the European Society for Medical Oncology.
[30] Katherine E Henson,et al. Cardiac Mortality Among 200 000 Five-Year Survivors of Cancer Diagnosed at 15 to 39 Years of Age , 2016, Circulation.
[31] K. S. Hall,et al. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial , 2016, The Lancet. Oncology.
[32] T. Dipetrillo,et al. Incidence, Treatment, and Survival Patterns for Sacral Chordoma in the United States, 1974–2011 , 2016, Front. Oncol..
[33] A. Pappo,et al. Comparison of 18F‐FDG‐PET‐CT and Bone Scintigraphy for Evaluation of Osseous Metastases in Newly Diagnosed and Recurrent Osteosarcoma , 2016, Pediatric blood & cancer.
[34] A. Liede,et al. Population-based study of giant cell tumor of bone in Sweden (1983-2011). , 2016, Cancer epidemiology.
[35] D. de Ruysscher,et al. Proton Therapy in Children: A Systematic Review of Clinical Effectiveness in 15 Pediatric Cancers. , 2016, International journal of radiation oncology, biology, physics.
[36] S. Ferrari,et al. Gemcitabine and docetaxel in relapsed and unresectable high-grade osteosarcoma and spindle cell sarcoma of bone , 2016, BMC Cancer.
[37] M. Díaz-Almirón,et al. Enchondroma versus Chondrosarcoma in Long Bones of Appendicular Skeleton: Clinical and Radiological Criteria—A Follow-Up , 2016, Journal of oncology.
[38] R. Grimer,et al. The prognostic and therapeutic factors which influence the oncological outcome of parosteal osteosarcoma. , 2015, The bone & joint journal.
[39] 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.
[40] J. Blay,et al. Sorafenib in patients with locally advanced and metastatic chordomas: a phase II trial of the French Sarcoma Group (GSF/GETO)† , 2015, Annals of oncology : official journal of the European Society for Medical Oncology.
[41] F. Bray,et al. Bone cancer incidence by morphological subtype: a global assessment , 2015, Cancer Causes & Control.
[42] D. Biau,et al. Mesenchymal chondrosarcoma: prognostic factors and outcome in 113 patients. A European Musculoskeletal Oncology Society study. , 2015, European journal of cancer.
[43] S. Stacchiotti,et al. Building a global consensus approach to chordoma: a position paper from the medical and patient community. , 2015, The Lancet. Oncology.
[44] K. S. Hall,et al. EURAMOS-1, an international randomised study for osteosarcoma: results from pre-randomisation treatment† , 2014, Annals of oncology : official journal of the European Society for Medical Oncology.
[45] A. Berner,et al. Time-trends on incidence and survival in a nationwide and unselected cohort of patients with skeletal osteosarcoma , 2014, Acta oncologica.
[46] P. Casali,et al. Sorafenib and everolimus combination in non-resectable high-grade osteosarcoma progressing after standard treatment: a non-randomized phase II clinical trial from the Italian Sarcoma Group. Abstract , 2022 .
[47] Steven S. Wong,et al. Regional variation and challenges in estimating the incidence of giant cell tumor of bone. , 2014, The Journal of bone and joint surgery. American volume.
[48] B. Yeap,et al. Long‐term results of Phase II study of high dose photon/proton radiotherapy in the management of spine chordomas, chondrosarcomas, and other sarcomas , 2014, Journal of surgical oncology.
[49] M. Stratton,et al. Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone , 2013, Nature Genetics.
[50] F. Bertucci,et al. Advanced chondrosarcomas: role of chemotherapy and survival. , 2013, Annals of oncology : official journal of the European Society for Medical Oncology.
[51] L. Mariani,et al. Phase II study on lapatinib in advanced EGFR-positive chordoma. , 2013 .
[52] W. Mendenhall,et al. Radiotherapy in the Management of Giant Cell Tumor of Bone , 2010, American journal of clinical oncology.
[53] C. Stiller,et al. Descriptive epidemiology of sarcomas in Europe: report from the RARECARE project. , 2013, European journal of cancer.
[54] P. Dileo,et al. Is [F-18]-fluorodeoxy-D-glucose positron emission tomography of value in the management of patients with craniofacial bone sarcomas undergoing neo-adjuvant treatment? , 2014, BMC Cancer.
[55] W. Tap,et al. Long‐term results (>25 years) of a randomized, prospective clinical trial evaluating chemotherapy in patients with high‐grade, operable osteosarcoma , 2012, Cancer.
[56] 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.
[57] A. McTiernan,et al. Incidence and survival of malignant bone sarcomas in England 1979–2007 , 2012, International journal of cancer.
[58] Gerald Antoch,et al. Oncologic PET/MRI, Part 2: Bone Tumors, Soft-Tissue Tumors, Melanoma, and Lymphoma , 2012, The Journal of Nuclear Medicine.
[59] R. Stupp,et al. Phase II study of imatinib in advanced chordoma. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[60] J. Wathen,et al. Phase II study of sequential gemcitabine followed by docetaxel for recurrent Ewing sarcoma, osteosarcoma, or unresectable or locally recurrent chondrosarcoma: results of Sarcoma Alliance for Research Through Collaboration Study 003. , 2012, The oncologist.
[61] U. Dirksen,et al. Risk of recurrence and survival after relapse in patients with Ewing sarcoma , 2011, Pediatric blood & cancer.
[62] R. Grimer,et al. The 'other' bone sarcomas: prognostic factors and outcomes of spindle cell sarcomas of bone. , 2011, The Journal of bone and joint surgery. British volume.
[63] W. Winkelmann,et al. The influence of tumor- and treatment-related factors on the development of local recurrence in osteosarcoma after adequate surgery. An analysis of 1355 patients treated on neoadjuvant Cooperative Osteosarcoma Study Group protocols. , 2011, Annals of oncology : official journal of the European Society for Medical Oncology.
[64] S. Ferrari,et al. Nonmetastatic Ewing family tumors: high-dose chemotherapy with stem cell rescue in poor responder patients. Results of the Italian Sarcoma Group/Scandinavian Sarcoma Group III protocol. , 2011, Annals of oncology : official journal of the European Society for Medical Oncology.
[65] D. Vanel,et al. Periosteal osteosarcoma , 2011, Cancer.
[66] 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.
[67] T. Triche,et al. Current treatment protocols have eliminated the prognostic advantage of type 1 fusions in Ewing sarcoma: a report from the Children's Oncology Group. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[68] U. Dirksen,et al. The value of local treatment in patients with primary, disseminated, multifocal Ewing sarcoma (PDMES) , 2010, Cancer.
[69] A. Llombart‐Bosch,et al. Molecular Diagnosis of Ewing Sarcoma Family of Tumors: A Comparative Analysis of 560 Cases With FISH and RT-PCR , 2009, Diagnostic molecular pathology : the American journal of surgical pathology, part B.
[70] R. Scholten,et al. Prognostic factors in localized extremity osteosarcoma: a systematic review. , 2009, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.
[71] L. Koniaris,et al. Ewing sarcoma demonstrates racial disparities in incidence‐related and sex‐related differences in outcome , 2009, Cancer.
[72] B. Massimo,et al. Phase 2 trial of two courses of cyclophosphamide and etoposide for relapsed high‐risk osteosarcoma patients , 2009 .
[73] Lisa Mirabello,et al. International osteosarcoma incidence patterns in children and adolescents, middle ages and elderly persons , 2009, International journal of cancer.
[74] D. Vanel,et al. Response to high‐dose ifosfamide in patients with advanced/recurrent Ewing sarcoma , 2009, Pediatric blood & cancer.
[75] Saskia Le Cessie,et al. Assessment of Interobserver Variability and Histologic Parameters to Improve Reliability in Classification and Grading of Central Cartilaginous Tumors , 2009, The American journal of surgical pathology.
[76] 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.
[77] J. Eary,et al. Imaging guidelines for children with Ewing sarcoma and osteosarcoma: A report from the Children's Oncology Group Bone Tumor Committee , 2008, Pediatric blood & cancer.
[78] S. Bielack,et al. Mesenchymal chondrosarcoma of soft tissues and bone in children, adolescents, and young adults , 2008, Cancer.
[79] P. Leavey,et al. Ewing sarcoma: prognostic criteria, outcomes and future treatment , 2008, Expert review of anticancer therapy.
[80] N. Willich,et al. Whole Lung Irradiation in Patients with Exclusively Pulmonary Metastases of Ewing Tumors , 2008, Strahlentherapie und Onkologie.
[81] H. Gelderblom,et al. The clinical approach towards chondrosarcoma. , 2008, The oncologist.
[82] Paul A Meyers,et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival--a report from the Children's Oncology Group. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[83] Thomas Völker,et al. Positron emission tomography for staging of pediatric sarcoma patients: results of a prospective multicenter trial. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[84] F. Sim,et al. Surgical Management of Conventional Grade I Chondrosarcoma of Long Bones , 2007, Clinical orthopaedics and related research.
[85] D. Biau,et al. Dedifferentiated chondrosarcoma: prognostic factors and outcome from a European group. , 2007, European journal of cancer.
[86] Michael Scholz,et al. Effectiveness of carbon ion radiotherapy in the treatment of skull-base chordomas. , 2007, International journal of radiation oncology, biology, physics.
[87] M. van Glabbeke,et al. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. , 2007, Journal of the National Cancer Institute.
[88] T. Peabody,et al. Staging of Primary Malignancies of Bone , 2006, CA: a cancer journal for clinicians.
[89] S. Bielack,et al. Current strategies of chemotherapy in osteosarcoma , 2006, International Orthopaedics.
[90] S. Henderson,et al. Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas , 2006, The Journal of pathology.
[91] S. Bielack,et al. Periosteal osteosarcoma--a European review of outcome. , 2005, European journal of cancer.
[92] S. Ferrari,et al. Neoadjuvant chemotherapy with high-dose Ifosfamide, high-dose methotrexate, cisplatin, and doxorubicin for patients with localized osteosarcoma of the extremity: a joint study by the Italian and Scandinavian Sarcoma Groups. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[93] M. Nooij,et al. Doxorubicin and cisplatin chemotherapy in high-grade spindle cell sarcomas of the bone, other than osteosarcoma or malignant fibrous histiocytoma: a European Osteosarcoma Intergroup Study. , 2005, European journal of cancer.
[94] J. Habrand,et al. Radiotherapeutic Factors in the Management of Cervical-basal Chordomas and Chondrosarcomas , 2004, Neurosurgery.
[95] F. Sim,et al. Dedifferentiated chondrosarcoma: the role of chemotherapy with updated outcomes. , 2004, The Journal of bone and joint surgery. American volume.
[96] T. Bauer,et al. Recommendations for the reporting of bone tumors. Association of Directors of Anatomic and Surgical Pathology. , 2004, Human pathology.
[97] S. Bielack,et al. Delaying surgery with chemotherapy for osteosarcoma of the extremities , 2004, Expert opinion on pharmacotherapy.
[98] P. Houghton,et al. Phase I Trial of Temozolomide and Protracted Irinotecan in Pediatric Patients with Refractory Solid Tumors , 2004, Clinical Cancer Research.
[99] 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.
[100] M. Link,et al. Presurgical chemotherapy compared with immediate surgery and adjuvant chemotherapy for nonmetastatic osteosarcoma: Pediatric Oncology Group Study POG-8651. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[101] 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.
[102] S. Ferrari,et al. Postrelapse survival in osteosarcoma of the extremities: prognostic factors for long-term survival. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[103] 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.
[104] S. Ferrari,et al. High-dose chemotherapy in the treatment of relapsed osteosarcoma: an Italian sarcoma group study. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[105] W. Winkelmann,et al. Prognostic factors in high-grade osteosarcoma of the extremities or trunk: an analysis of 1,702 patients treated on neoadjuvant cooperative osteosarcoma study group protocols. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[106] R. Grimer,et al. Risk factors for survival and local control in chondrosarcoma of bone. , 2002, The Journal of bone and joint surgery. British volume.
[107] D. Vanel,et al. Computed tomography of pulmonary metastases from osteosarcoma: the less poor technique. A study of 51 patients with histological correlation. , 2001, Annals of oncology : official journal of the European Society for Medical Oncology.
[108] 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.
[109] 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.
[110] S. Ferrari,et al. Prognostic factors in nonmetastatic Ewing's sarcoma of bone treated with adjuvant chemotherapy: analysis of 359 patients at the Istituto Ortopedico Rizzoli. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[111] M. van Glabbeke,et al. Neoadjuvant chemotherapy with doxorubicin and cisplatin in malignant fibrous histiocytoma of bone: A European Osteosarcoma Intergroup study. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[112] H. Avet-Loiseau,et al. Ifosfamide and etoposide in childhood osteosarcoma. A phase II study of the French Society of Paediatric Oncology. , 1997, European journal of cancer.
[113] P. Picci,et al. Relationship of chemotherapy-induced necrosis and surgical margins to local recurrence in osteosarcoma. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[114] H. Kovar,et al. Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data. , 1994, British Journal of Cancer.
[115] P. Sorensen,et al. A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS–family transcription factor, ERG , 1994, Nature Genetics.
[116] 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.
[117] H. Mankin,et al. The hazards of biopsy in patients with malignant primary bone and soft-tissue tumors. , 1982, The Journal of bone and joint surgery. American volume.
[118] W. Enneking,et al. A System for the Surgical Staging of Musculoskeletal Sarcoma , 1980, Clinical orthopaedics and related research.