Literature DB >> 27482030

Ewing's sarcoma: only patients with 100% of necrosis after chemotherapy should be classified as having a good response.

J I Albergo1, C L Gaston1, M Laitinen1, A Darbyshire1, L M Jeys1, V Sumathi1, M Parry1, D Peake1, S R Carter1, R Tillman1, A T Abudu1, R J Grimer1.   

Abstract

AIMS: The purpose of this study was to review a large cohort of patients and further assess the correlation between the histological response to chemotherapy in patients with Ewing's sarcoma with the overall (OS) and event-free survival (EFS). PATIENTS AND METHODS: All patients treated for Ewing's sarcoma between 1980 and 2012 were reviewed. Of these, 293 patients without metastases at the time of diagnosis and treated with chemotherapy and surgery were included. Patients were grouped according to the percentage of necrosis after chemotherapy: Group I: 0% to 50%, Group II: 51% to 99% and Group III: 100%.
RESULTS: The mean age at diagnosis was 16 years (1 to 62) and the mean follow-up was 9.1 years (six months to 32.6 years). The OS and EFS for the series were 75% and 65% at five years. There were significant differences in survival between the groups of necrosis: 0% to 50% (OS: 49% and EFS: 45% at five years, respectively) compared with 51% to 99% (OS: 72% and EFS: 59% at five years, respectively) and 100% (OS: 94% and EFS: 81% at five years, respectively) (p < 0.001). There were no significant differences in survival between patients treated between 1980 and 1989 compared with those treated between 1990 and 1999, and those treated between 2000 and 2012 (p = 0.55).
CONCLUSION: Only patients with 100% necrosis after chemotherapy should be classified as having a good response to chemotherapy because they have significantly better rates of survival compared with those with any viable tumour in the surgical specimen. Cite this article: Bone Joint J 2016;98-B:1138-44. ©2016 The British Editorial Society of Bone & Joint Surgery.

Entities:  

Keywords:  Event free survival; Ewing sarcoma; Histological response; Overall survival

Mesh:

Year:  2016        PMID: 27482030     DOI: 10.1302/0301-620X.98B8.37346

Source DB:  PubMed          Journal:  Bone Joint J        ISSN: 2049-4394            Impact factor:   5.082


  14 in total

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2.  Curettage, phenolization, and cementation in paediatric Ewing's sarcoma with a complete radiological response to neoadjuvant chemotherapy.

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4.  Single-Centre Experience of Systemic Treatment with Vincristine, Ifosfamide, and Doxorubicin Alternating with Etoposide, Ifosfamide, and Cisplatin in Adult Patients with Ewing Sarcoma.

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6.  Easy-to-use clinical tool for survival estimation in Ewing sarcoma at diagnosis and after surgery.

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Review 7.  Proteomic research in sarcomas - current status and future opportunities.

Authors:  Jessica Burns; Christopher P Wilding; Robin L Jones; Paul H Huang
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9.  Dynamic prediction of overall survival: a retrospective analysis on 979 patients with Ewing sarcoma from the German registry.

Authors:  Chuchu Liu; Anja J Rueten-Budde; Andreas Ranft; Uta Dirksen; Hans Gelderblom; Marta Fiocco
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