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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

医学 依托泊苷 横纹肌肉瘤 原发性肿瘤 软组织肉瘤 危险系数 转移瘤切除术 外科 淋巴结 肉瘤 异环磷酰胺 肿瘤科 软组织 内科学 化疗 癌症 转移 置信区间 病理
作者
Amadeus T. Heinz,Anton Schönstein,Martin Ebinger,Jörg Fuchs,Beate Timmermann,Guido Seitz,Christian Vokuhl,Marc Münter,Kristian W. Pajtler,Sabine Stegmaier,Thekla von Kalle,Christian P. Kratz,Gustaf Ljungman,Hanna Juntti,Thomas Klingebiel,Ewa Kościelniak,Monika Sparber‐Sauer,the Cooperative Weichteilsarkom Studiengruppe
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:71 (1) 被引量:14
标识
DOI:10.1002/pbc.30707
摘要

Abstract Background Outcome 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. Procedure Patients 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. Results In 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). Conclusions Prognosis 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.
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