Metastatic adult‐type non‐rhabdomyosarcoma soft tissue sarcomas in children and adolescents: A cohort study from the European paediatric Soft tissue sarcoma Study Group

Author:

Ferrari Andrea1ORCID,Orbach Daniel2ORCID,Casanova Michela1,van Noesel Max M.3,Berlanga Pablo4,Brennan Bernadette5,Corradini Nadege6,Schoot Reineke A.3,Ramirez‐Villar Gema L.7,Hjalgrim Lisa Lyngsie8,Alaggio Rita9,Guillen Burrieza Gabriela10,Safwat Akmal11,Cameron Alison L.12,van Rijn Rick R.13,Minard‐Colin Veronique4ORCID,Zanetti Ilaria14,Bisogno Gianni1415ORCID,Chisholm Julia C.16,Merks Johannes H. M.317

Affiliation:

1. Pediatric Oncology Unit Fondazione IRCCS Istituto Nazionale Tumori Milano Italy

2. SIREDO Oncology Center Institut Curie PSL University Paris France

3. Princess Máxima Center for Pediatric Oncology Utrecht Netherlands

4. Department of Pediatric and Adolescent Oncology Gustave‐Roussy Cancer Campus Université Paris‐Saclay Villejuif France

5. Pediatric Oncology Royal Manchester Children's Hospital Manchester UK

6. Department of Pediatric Oncology Institut d’Hematologie et d’Oncologie Pédiatrique,/Centre Léon Bérard Lyon France

7. Pediatric Oncology Unit Hospital Universitario Virgen del Rocío Sevilla Spain

8. Department of Pediatrics and Adolescent Medicine Rigshospitalet University of Copenhagen Copenhagen Denmark

9. Pathology Department Ospedale Pediatrico Bambino Gesù IRCCS Rome Italy

10. Surgical Oncology and Neonatal Surgery Pediatric Surgery Department Hospital Infantil Universitari Vall d’Hebron Barcelona Spain

11. Oncology Department and Danish Center for Particle Therapy Aarhus University Hospital Aarhus Denmark

12. Bristol Haematology and Oncology Centre University Hospitals Bristol and Weston NHS Foundation Trust Bristol UK

13. Department of Radiology and Nuclear Medicine UMC University of Amsterdam Amsterdam Netherlands

14. Pediatric Hematology Oncology Division University Hospital of Padua Padua Italy

15. Department of Women's and Children's Health University of Padua Padua Italy

16. Children and Young People's Unit The Royal Marsden Hospital and Institute of Cancer Research Sutton UK

17. Division of Imaging and Oncology University Medical Center Utrecht Utrecht University Utrecht The Netherlands

Abstract

AbstractBackgroundLimited data exist on the clinical behavior of pediatric non‐rhabdomyosarcoma soft tissue sarcomas (NRSTS) with distant metastases at onset, and a clear standard of care has not yet been defined.MethodsThis cohort study reports on pediatric adult‐type metastatic NRSTS enrolled in two concurrent prospective European studies, i.e., the randomized BERNIE study and the single‐arm MTS 2008 study developed by the European paediatric Soft tissue sarcoma Study Group. Treatment programs were originally designed for patients with metastatic rhabdomyosarcoma, i.e., nine courses of multidrug chemotherapy (with or without bevacizumab in the BERNIE study), followed by 12 cycles of maintenance therapy, whereas radiotherapy and/or surgery (on primary tumor and/or metastases) were delayed until after seven courses of chemotherapy had been administered.ResultsThe study included 61 patients <21 years old treated from July 2008 to December 2016. The lung was the site of metastases in 75% of the cases. All patients received multi‐agent chemotherapy, 44% had local therapy to primary tumor, and 18% had treatment of metastases. Median time to progression/relapse was 6 months. A high rate of tumor progression was observed during the initial part of the chemotherapy program. With a median follow‐up of 41.5 months (range, 2–111 months), 3‐year event‐free survival and overall survival were 15.4% (95% confidence interval [CI], 7.6–25.7) and 34.9% (95% CI, 22.7–47.5), respectively. There were no statistically significant differences in outcome depending on the type of treatment administered.ConclusionsThe study confirmed the overall poor outcome for patients with metastatic NRSTS, whose treatment remains a challenge.Plain Language Summary Pediatric non‐rhabdomyosarcoma soft tissue sarcomas form a heterogeneous group of rare tumors. Although recent international studies have defined the standard of care for patients with localized disease, limited data are available on the clinical behavior of patients with distant metastases. This study on 61 metastatic cases treated on two prospective European protocols confirms that the chances of survival of such patients are often dismal and a standard treatment is still lacking.

Publisher

Wiley

Subject

Cancer Research,Oncology

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