Total body MRI-governed involved compartment irradiation combined with high-dose chemotherapy and stem cell rescue improves long-term survival in Ewing tumor patients with multiple primary bone metastases

S. Burdach*, U. Thiel, M. Schöniger, R. Haase, A. Wawer, M. Nathrath, H. Kabisch, C. Urban, H. J. Laws, U. Dirksen, M. Steinborn, J. Dunst, H. Jürgens

*Corresponding author for this work
34 Citations (Scopus)

Abstract

We examined the role of total body magnetic resonance imaging (TB-MRI)-governed involved compartment irradiation (ICI) and high-dose chemotherapy (HDC), followed by stem cell rescue (SCR) in patients with high-risk Ewing tumors (ETs) with multiple primary bone metastases (high-risk ET-MBM). Eleven patients with high-risk ET-MBM receiving initial assessment of involved bones by TB-MRI were registered from 1995 to 2000 (group A). In all, 6 patients out of 11 had additional lung disease at initial diagnosis; all had multifocal bone disease with more than three bones involved. After systemic induction with etoposide, vincristine, adriamycin (doxorubicin), ifosfamide, and actinomycin D (EVAIA) or VAIA chemotherapy, ICI of all sites positive by TB-MRI was administered, followed by HDC and SCR. A second group matched for observation period and consisting of 26 patients with more than three involved bones at diagnosis was treated with the European Intergroup Cooperative Ewing Sarcoma Study-92 (EICESS-92) protocol (group B). These patients did not receive TB-MRI and consequently did not receive TB-MRI-governed ICI, or HDC and SCR. Survival in group A vs group B was 45 vs 8 at 5 years and 27 vs 8 at 10 years after diagnosis (log rank and Breslow: P<0.005). We conclude that TB-MRI-governed ICI followed by HDC and SCR in ET-MBM is feasible and warrants further evaluation in prospective studies.

Original languageEnglish
JournalBone Marrow Transplantation
Volume45
Issue number3
Pages (from-to)483-489
Number of pages7
ISSN0268-3369
DOIs
Publication statusPublished - 01.01.2010

Funding

We thank B Metzner, Klinikum Oldenburg, Department of Hematology and Oncology, Oldenburg, and B Kremens, Department of Pediatric Hematology-Oncology, University of Essen, Essen; and the respective institutions for their participation in the study. This study was supported by unrestricted grants to SB from the Wilhelm Sander-Stiftung (2006.109.1), Else Kroener–Fresenius–Stiftung (P31/08//A123/07), BMBF (TranSarNet FK:01GM0870), AmGen and Chugai.

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