Literature DB >> 25163763

Validation of a multi-modal treatment protocol for Ewing sarcoma--a report from the polish pediatric oncology group.

Anna Raciborska1, Katarzyna Bilska, Katarzyna Drabko, Radosław Chaber, Grażyna Sobol, Monika Pogorzała, Elżbieta Wyrobek, Katarzyna Połczyńska, Elżbieta Rogowska, Carlos Rodriguez-Galindo, Wojciech Wożniak.   

Abstract

BACKGROUND: Ewing sarcoma (ES) is the second most common paediatric malignant bone tumor. Advances in multi-disciplinary care have resulted in significant improvement in cure rates over the last decades. However, the generalization of those results in countries traditionally excluded from large cooperative trials has yet to be demonstrated. We report the results of modern multi-disciplinary care for patients with ES in Poland. PROCEDURES: One hundred and thirty-two patients with ES were treated using modern multi-modal therapy during the period 2000-2009. Overall survival was estimated by Kaplan-Meier methods and compared using long-rank test and Cox models. Factors predictive of outcome in our setting were analyzed to identify distinct risk groups that could help identify areas for improvement.
RESULTS: The median age at the time of diagnosis was 12.3 years. With a median follow-up of 5.0 years, the 5-year event-free survival (EFS) and OS estimates for localized disease were 54.88% and 68.29%, respectively. For patients with metastatic disease, 5-year EFS and OS estimates were 36% and 42%, respectively. There was no correlation between age and stage or site. Patients with localized, non-pelvic disease had better outcome than patients with axial tumors (71% vs. 44%, respectively, P = 0.00073). Treatment failure was associated with stage, pelvic primary, poor histological response, and type of local control.
CONCLUSIONS: Successful treatment of ES requires optimal systemic and local therapy. We were able to replicate the results of modern multi-modal protocols. Validation of current treatment protocols in countries with more limited cancer treatment resources is required.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  Ewing sarcoma; children; survival; treatment

Mesh:

Substances:

Year:  2014        PMID: 25163763     DOI: 10.1002/pbc.25167

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  8 in total

1.  Response to chemotherapy estimates by FDG PET is an important prognostic factor in patients with Ewing sarcoma.

Authors:  A Raciborska; K Bilska; K Drabko; E Michalak; R Chaber; M Pogorzała; K Połczyńska; G Sobol; M Wieczorek; K Muszyńska-Rosłan; M Rychlowska-Pruszyńska; C Rodriguez-Galindo; M Dziuk
Journal:  Clin Transl Oncol       Date:  2015-08-07       Impact factor: 3.405

2.  Efficacy of replacing actinomycin-D with carboplatin in Ewing sarcoma consolidation treatment: Single-center experience.

Authors:  Ayşe Özkan; İbrahim Bayram; Gülay Sezgin; Akif Mirioğlu; Serhan Küpeli
Journal:  J Bone Oncol       Date:  2022-05-25       Impact factor: 4.491

3.  CNS Metastases from Bone and Soft Tissue Sarcomas in Children, Adolescents, and Young Adults: Are They Really So Rare?

Authors:  Monika Bekiesinska-Figatowska; Agnieszka Duczkowska; Marek Duczkowski; Hanna Bragoszewska; Anna Romaniuk-Doroszewska; Beata Iwanowska; Sylwia Szkudlinska-Pawlak; Jaroslaw Madzik; Katarzyna Bilska; Anna Raciborska
Journal:  Biomed Res Int       Date:  2017-01-24       Impact factor: 3.411

4.  Prediction of Ewing Sarcoma treatment outcome using attenuated tissue reflection FTIR tissue spectroscopy.

Authors:  Radosław Chaber; Kornelia Łach; Christopher J Arthur; Anna Raciborska; Elżbieta Michalak; Krzysztof Ciebiera; Katarzyna Bilska; Katarzyna Drabko; Józef Cebulski
Journal:  Sci Rep       Date:  2018-08-17       Impact factor: 4.379

5.  Sorafenib in patients with progressed and refractory bone tumors.

Authors:  Anna Raciborska; Katarzyna Bilska
Journal:  Med Oncol       Date:  2018-08-16       Impact factor: 3.064

6.  Clinical Characteristics and Treatment Outcomes of Myeloid Sarcoma in Children: The Experience of the Polish Pediatric Leukemia and Lymphoma Study Group.

Authors:  Magdalena Samborska; Małgorzata Barańska; Jacek Wachowiak; Jolanta Skalska-Sadowska; Sheanda Thambyrajah; Małgorzata Czogała; Walentyna Balwierz; Sylwia Kołtan; Katarzyna Peszyńska-Żelazny; Mariusz Wysocki; Tomasz Ociepa; Tomasz Urasiński; Grażyna Wróbel; Jadwiga Węcławek-Tompol; Bogna Ukielska; Alicja Chybicka; Anna Kitszel; Maryna Krawczuk-Rybak; Anna Szmydki-Baran; Iwona Malinowska; Michał Matysiak; Agnieszka Mizia-Malarz; Renata Tomaszewska; Tomasz Szczepański; Agnieszka Chodała-Grzywacz; Grażyna Karolczyk; Lucyna Maciejka-Kembłowska; Ninela Irga-Jaworska; Wanda Badowska; Michał Dopierała; Paweł Kurzawa; Katarzyna Derwich
Journal:  Front Oncol       Date:  2022-07-07       Impact factor: 5.738

7.  Distinguishing Ewing sarcoma and osteomyelitis using FTIR spectroscopy.

Authors:  Radosław Chaber; Christopher J Arthur; Joanna Depciuch; Kornelia Łach; Anna Raciborska; Elżbieta Michalak; Józef Cebulski
Journal:  Sci Rep       Date:  2018-10-10       Impact factor: 4.379

8.  Double Endoprosthesis in the Management of Refractory Metastatic Primary Bone Tumors in Children and Young Adults.

Authors:  Anna Raciborska; Iwona Malesza; Katarzyna Bilska; Tomasz Koziński; Bartosz Pachuta
Journal:  Adv Orthop       Date:  2021-07-23
  8 in total

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