Ewing family tumors of the appendicular skeleton: a retrospective analysis of prognostic factors-Reference-Cited by-同舟云学术

Ewing family tumors of the appendicular skeleton: a retrospective analysis of prognostic factors

Published:2021-07-29 Issue:8 Volume:31 Page:1557-1565
ISSN:1633-8065
Container-title:European Journal of Orthopaedic Surgery & Traumatology
language:en
Short-container-title:Eur J Orthop Surg Traumatol

Author:

Muratori Francesco^ORCID,Foschi Lorenzo,Roselli Giuliana,Frenos Filippo,Tamburini Angela,Palomba Annarita,Greto Daniela,Loi Mauro,Beltrami Giovanni,Capanna Rodolfo,Mondanelli Nicola,Campanacci Domenico Andrea

Publisher

Springer Science and Business Media LLC

Subject

Orthopedics and Sports Medicine,Surgery

Link

https://link.springer.com/content/pdf/10.1007/s00590-021-03077-y.pdf

Reference36 articles.

1. Bosma SE, Ayua O, Fiocco M, Gelderblom H, Dijkstra PDS (2018) Prognostic factors for survival in Ewing sarcoma: a systematic review. Surg Onc 27(4):603–610

2. Zhou Q, Wu ZY, Lin ZQ (2019) A nomogram to predict prognosis in Ewing sarcoma of bone. J Bone Oncol 15:100223

3. Ferrari S, Sundby Hall K, Luksch R, Tienghi A, Wiebe T, Fagioli F, Alvegard TA, Brach Del Prever A, Tamburini A, Alberghini M, Gandola L, Mercuri M, Capanna R, Mapelli S, Prete A, Carli M, Picci P, Barbieri E, Bacci G, Smeland S (2011) Non-metastatic 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. Ann Oncol 22(5):1221–1227

4. Berger M, Fagioli F, Abate M, Riccardi R, Prete A, Cozza R, Bertulli R, Podda M, Ferrari S, Luksch R (2013) Unusual sites of Ewing sarcoma (ES): a retrospective multicenter 30-year experience of the Italian association of pediatric hematology and oncology (AIEOP) and Italian sarcoma group (ISG). Eur J Cancer 49(17):3658–3665

5. Marina NM, Pappo AS, Parham DM, Cain AM, Rao BN, Poquette CA, Pratt CB, Greenwald C, Meyer WH (1999) Chemotherapy–dose intensification for pediatric patients with Ewing’s family of tumors and desmoplastic small round cell tumor: a feasibility study at St. Jude children’s research hospital. J Clin Oncol 17(1):180–190