Long-Term Analysis of Patients With Ewing Sarcoma Included in the Euro-EWING99 Study

T Thibaud Valentin S Sarah Winter (Institut Curie, Paris, France) U Uta Dirksen D Douglas S. Hawkins (Seattle Children's Hospital, University of Washington, Seattle, WA) H Hans Gelderblom S Séverine Risbourg (Centre Oscar Lambret, Lille, France) P Pablo Berlanga (Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France) N Nathalie Gaspar K Katerine A. Janeway (Dana-Farber/Children's Hospital Cancer Center, Boston, MA) H Heribert Juergens (University Children's Hospital Münster, West German Cancer Center Network, Muenster, Germany) I Ina Elisa Kirchberg (Children's Hospital, University of Duisburg-Essen, Essen, Germany) R Ruth Ladenstein (St Anna Children's Cancer Research Institute CCRI, Vienna, Austria) V Valérie Laurence (Institut Curie, Paris, France) M Marie-Cécile Le Deley (Centre Oscar Lambret, Lille, France) M Martin G. McCabe (Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom) H Hans Merks (Princess Máxima Center, Utrecht, the Netherlands) A Andreas Ranft S Sandra Strauss (UCL Cancer Institute, University College London, London, United Kingdom) M Michiel A.J. Van De Sande (Leiden University Medical Center, Leiden, the Netherlands) J Jeremy Whelan (University College London Hospitals NHS Foundation Trust, London, United Kingdom) P Perrine Marec-Bérard (1Institute of Hematology and Pediatric Oncology, Centre Leon-Berard, Lyon, France) B Bernadette Brennan (Royal Manchester Hospital, Manchester, United Kingdom)

Abstract

PURPOSE Euro-EWING99 study was a large, international, prospective study recruiting patients with Ewing sarcoma (EWS) between 1999 and 2015. It assessed three different clinical questions through randomized trials. We report here the characteristics and outcomes of all patients. METHODS Patients younger than 50 years with EWS were included in the study. They received induction chemotherapy (six courses of vincristine [day 1], ifosfamide [day 1-3], doxorubicin [day 1-3], and etoposide [day 1-3; VIDE], administered every 3 weeks), local therapy (surgery/radiotherapy), and different consolidation treatments according to clinical risk group and trial. The objectives of the study were to describe the entire cohort according to the initial staging group, to describe the survival outcomes (overall survival [OS]; progression-free survival [PFS]; and local control), and to evaluate prognostic factors associated with OS and PFS. RESULTS Three thousand three hundred ninety-five patients were included in the study, including 2,267 with a localized disease, 614 with pleuropulmonary metastases, and 514 with extrapulmonary metastases. Ninety-eight percent of patients received ≥4 neoadjuvant VIDE courses. The modalities of local treatment and consolidation therapy differed among the three staging groups. With a median follow-up of 7.2 years, PFS of the entire cohort was 60.2% and 55.4% at 3 and 5 years, respectively. OS was 72.6% and 64.6% at 3 and 5 years, respectively. In addition to metastatic status at diagnosis, main prognostic factors included patient age, tumor volume, and histologic response both for PFS and OS, independent of metastatic status. CONCLUSION To our knowledge, this study is the largest published series of patients with EWS and may serve as a landmark paper for EWS. It confirms the major prognostic value of the complete histologic response after neoadjuvant therapy.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 31, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (22)

T

Thibaud Valentin

S

Sarah Winter

Institut Curie, Paris, France

U

Uta Dirksen

D

Douglas S. Hawkins

Seattle Children's Hospital, University of Washington, Seattle, WA

H

Hans Gelderblom

S

Séverine Risbourg

Centre Oscar Lambret, Lille, France

P

Pablo Berlanga

Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France

N

Nathalie Gaspar

K

Katerine A. Janeway

Dana-Farber/Children's Hospital Cancer Center, Boston, MA

H

Heribert Juergens

University Children's Hospital Münster, West German Cancer Center Network, Muenster, Germany

I

Ina Elisa Kirchberg

Children's Hospital, University of Duisburg-Essen, Essen, Germany

R

Ruth Ladenstein

St Anna Children's Cancer Research Institute CCRI, Vienna, Austria

V

Valérie Laurence

Institut Curie, Paris, France

M

Marie-Cécile Le Deley

Centre Oscar Lambret, Lille, France

M

Martin G. McCabe

Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom

H

Hans Merks

Princess Máxima Center, Utrecht, the Netherlands

A

Andreas Ranft

S

Sandra Strauss

UCL Cancer Institute, University College London, London, United Kingdom

M

Michiel A.J. Van De Sande

Leiden University Medical Center, Leiden, the Netherlands

J

Jeremy Whelan

University College London Hospitals NHS Foundation Trust, London, United Kingdom

P

Perrine Marec-Bérard

1Institute of Hematology and Pediatric Oncology, Centre Leon-Berard, Lyon, France

B

Bernadette Brennan

Royal Manchester Hospital, Manchester, United Kingdom