Significance of fusion status, Oberlin risk factors, local and maintenance treatment in pediatric and adolescent patients with metastatic rhabdomyosarcoma: Data of the European Soft Tissue Sarcoma Registry SoTiSaR

Author:

Heinz Amadeus T.12ORCID,Schönstein Anton3,Ebinger Martin1,Fuchs Jörg4,Timmermann Beate5,Seitz Guido6,Vokuhl Christian7,Münter Marc8,Pajtler Kristian W.91011,Stegmaier Sabine2,von Kalle Thekla12,Kratz Christian P.13,Ljungman Gustaf14,Juntti Hanna15,Klingebiel Thomas16,Koscielniak Ewa217,Sparber‐Sauer Monika217,

Affiliation:

1. Department of Pediatric Hematology and Oncology University Children´s Hospital Tuebingen Tuebingen Germany

2. Stuttgart Cancer Center Zentrum für Kinder‐, Jugend‐ und Frauenmedizin (Olgahospital), Pädiatrie 5 (Pädiatrische Onkologie, Hämatologie, Immunologie) Klinikum der Landeshauptstadt Stuttgart Stuttgart Germany

3. Network Aging Research Heidelberg University Heidelberg Germany

4. Department of Pediatric Surgery and Urology University Children's Hospital Tuebingen Germany

5. Department of Particle Therapy, West German Proton Therapy Centre Essen (WPE) University Medical Center Essen, West German Cancer Center (WTZ) German Cancer Consortium (DKTK) Essen Germany

6. Department of Pediatric Surgery and Urology University Hospital Giessen‐Marburg Marburg Germany

7. Section of Pediatric Pathology Department of Pathology Bonn Germany

8. Stuttgart Cancer Center Department of Radiation Oncology Klinikum der Landeshauptstadt Stuttgart Stuttgart Germany

9. Hopp Children's Cancer Center Heidelberg (KiTZ) Heidelberg University Heidelberg Germany

10. Division of Pediatric Neurooncology German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK) Heidelberg University Heidelberg Germany

11. Department of Pediatric Oncology, Hematology, and Immunology Heidelberg University Hospital Heidelberg Germany

12. Stuttgart Cancer Center, Zentrum für Kinder‐, Jugend‐ und Frauenmedizin (Olgahospital), Department of Radiology Klinikum der Landeshauptstadt Stuttgart Stuttgart Germany

13. Pediatric Hematology and Oncology Hannover Medical School Hannover Germany

14. Department of Women's and Children's Health Children's University Hospital University of Uppsala Uppsala Sweden

15. Department of Pediatrics and Adolescence Oulu University Hospital Oulu Finland

16. Department of Children and Adolescents University Hospital of Frankfurt Frankfurt Germany

17. Medical Faculty University Tübingen Tübingen Germany

Abstract

AbstractBackgroundOutcome of primary metastatic rhabdomyosarcoma (RMS) is poor. Certain risk factors as fusion status, Oberlin score, and local treatment of primary tumor are known to influence prognosis.ProcedurePatients with metastatic RMS were treated according to Cooperative Weichteilsarkom Studiengruppe (CWS) guidance with chemotherapy (CHT), radiotherapy (RT) excluding total lung irradiation (TLI), complete resection of the primary tumor, and metastasectomy if possible. Kaplan–Meier estimators and Cox proportional hazard models were used to examine event‐free survival (EFS) and overall survival (OS) involving also landmark analyses.ResultsIn the European Soft Tissue Sarcoma Registry SoTiSaR (2009–2018), 211 patients were analyzed. Many patients had fusion‐positive alveolar RMS (n = 83; 39%). Median age was 9.4 years [0.1–19.7 years]. Treatment primarily consisted of CHT with CEVAIE (carboplatin, epirubicine, vincristine, actinomycin‐D, ifosfamide, etoposide: 86%, other regimens: 14%), RT (71%), resection of primary tumor (37%), metastasectomy (19%), and lymph node sampling/dissection (21%). Maintenance treatment (MT) (oral trofosfamide, idarubicin, etoposide) was added in 74% of patients. Oberlin factors, fusion status, and MT were predictive for EFS and OS. MT with O‐TIE was not improving outcome when adjusting for the immortal time bias. Local treatment of the primary tumor and radical irradiation (except TLI) improved EFS, not OS, when adjusting for the Oberlin score. Patients with fusion‐negative alveolar RMS (n = 9) had an excellent outcome with a 5‐year EFS and OS of 100%, compared to patients with embryonal RMS (49%/62%), PAX7‐ (22%/47%) and PAX3/FOXO1‐positive ARMS (10/13%), respectively (p < .001).ConclusionsPrognosis of metastatic RMS primarily depends on fusion status and Oberlin score. Fusion status needs to be considered in future trials to optimize treatment outcome. The role of radical irradiation needs further investigation.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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