Metastatic Rhabdomyosarcoma: Results of the European Paediatric Soft Tissue Sarcoma Study Group MTS 2008 Study and Pooled Analysis With the Concurrent BERNIE Study

Author:

Schoot Reineke A.1ORCID,Chisholm Julia C.2ORCID,Casanova Michela3ORCID,Minard-Colin Veronique4ORCID,Geoerger Birgit45ORCID,Cameron Alison L.6ORCID,Coppadoro Beatrice7,Zanetti Ilaria7,Orbach Daniel8ORCID,Kelsey Anna9,Rogers Timothy10,Guizani Cecile11,Elze Markus11,Ben-Arush Myriam12,McHugh Kieran13,van Rijn Rick R.14ORCID,Ferman Sima15,Gallego Soledad16ORCID,Ferrari Andrea3ORCID,Jenney Meriel17,Bisogno Gianni7ORCID,Merks Johannes H.M.1ORCID

Affiliation:

1. Princess Máxima Centre for Paediatric Oncology, Utrecht, the Netherlands

2. Children and Young Peoples Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton, Surrey, United Kingdom

3. Paediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

4. Gustave-Roussy Cancer Campus, Department of Paediatric and Adolescent Oncology, Université Paris-Saclay, Villejuif, France

5. Gustave-Roussy Cancer Campus, INSERM U1015, Université Paris Saclay, Villejuif, France

6. Bristol Haematology and Oncology Centre, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom

7. Haematology Oncology Division, Department of Women's and Children's Health, University of Padova, Padova, Italy

8. SIREDO Oncology Center, Institut Curie, PSL University, Paris, France

9. Department of Paediatric Histopathology, Royal Manchester Children's Hospital, Manchester, United Kingdom

10. Department of Pediatric Surgery, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom

11. F. Hoffmann-La Roche Ltd, Basel, Switzerland

12. Joan and Sanford Weill Pediatric Hematology Oncology and Bone Marrow Transplantation Division, Ruth Rappaport Children's Hospital, Rambam Medical Center, Haifa, Israel

13. Department of Radiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom

14. Department of Radiology and Nuclear Medicine, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, the Netherlands

15. Instituto Nacional de Câncer, Pediatric Oncology Department, Rio de Janeiro, RJ, Brazil

16. Pediatric Oncology, Vall d'Hebron University Hospital, Barcelona, Spain

17. Department of Paediatric Oncology, Children's Hospital for Wales, Heath Park, Cardiff, United Kingdom

Abstract

PURPOSE Outcome for patients with metastatic rhabdomyosarcoma (RMS) is poor. This study presents the results of the MTS 2008 study with a pooled analysis including patients from the concurrent BERNIE study. PATIENTS AND METHODS In MTS 2008, patients with metastatic RMS received four cycles of ifosfamide, vincristine, and actinomycin D (IVA) plus doxorubicin, five cycles of IVA, and 12 cycles of maintenance chemotherapy (low-dose cyclophosphamide and vinorelbine). The BERNIE study randomly assigned patients to the addition or not of bevacizumab to the same chemotherapy. Local therapy (surgery/radiotherapy) was given to the primary tumor and all metastatic sites when feasible. RESULTS MTS 2008 included 270 patients (median age, 9.6 years; range, 0.07-20.8 years). With a median follow-up of 50.3 months, 3-year event-free survival (EFS) and overall survival (OS) were 34.9% (95% CI, 29.1 to 40.8) and 47.9% (95% CI, 41.6 to 53.9), respectively. In pooled analyses on 372 patients with a median follow-up of 55.2 months, 3-year EFS and OS were 35.5% (95% CI, 30.4 to 40.6) and 49.3% (95% CI, 43.9 to 54.5), respectively. Patients with ≤ 2 Oberlin risk factors (ORFs) had better outcome than those with ≥ 3 ORFs: 3-year EFS was 46.1% versus 12.5% ( P < .0001) and 3-year OS 60.0% versus 26.0% ( P < .0001). Induction chemotherapy and maintenance appeared tolerable; however, about two third of patients needed dose adjustments during maintenance. CONCLUSION Outcome remains poor for patients with metastatic RMS and multiple ORFs. Because of the design of the studies, it was not possible to determine whether the intensive induction regimen and/or the addition of maintenance treatment resulted in apparent improvement of outcome compared with historical cohorts. Further studies, with novel treatment approaches are urgently needed, to improve outcome for the group of patients with adverse prognostic factors.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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