Tramsen, Lars; Bochennek, Konrad; Sparber-Sauer, Monika; Salzmann-Manrique, Emilia; Scheer, Monika; Dantonello, Tobias; Borkhardt, Arndt; Dirksen, Uta; Thorwarth, Anne; Greiner, Jeanette; Ebinger, Martin; Weclawek-Tompol, Jadwiga; Ladenstein, Ruth; Ljungman, Gustaf; Hallmen, Erika; Lehrnbecher, Thomas; Koscielniak, Ewa; Klingebiel, Thomas (2023). Pediatric Patients with Stage IV Rhabdomyosarcoma Significantly Benefit from Long-Term Maintenance Therapy: Results of the CWS-IV 2002 and the CWS DOK IV 2004-Trials. Cancers, 15(7) MDPI AG 10.3390/cancers15072050
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Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma (STS) in childhood. Whereas more than 90% of patients with localized low-risk RMS can be cured, metastatic RMS have a dismal outcome, with survival rates of less than 30%. The HD CWS-96 trial showed an improved outcome for patients receiving maintenance therapy after completing intensive chemotherapy. Consequently, the international clinical trials CWS-IV 2002 and CWS DOK IV 2004 on metastatic disease of STS of the Cooperative Weichteilsarkom Studiengruppe (CWS) were designed in addition to the CWS-2002P trial for localized RMS disease. All patients received a multimodal intensive treatment regimen. To maintain remission, three options were compared: long-term maintenance therapy (LTMT) versus allogeneic hematopoietic stem cell transplantation (alloHSCT) versus high-dose chemotherapy (HDCT). A total of 176 pediatric patients with a histologically confirmed diagnosis of metastatic RMS or RMS-like tumor were included. A total of 89 patients receiving LTML showed a significantly better outcome, with an event-free survival (EFS) of 41% and an overall survival (OS) of 53%, than alloHSCT (n = 21, EFS 19%, p = 0.02, OS 24%, p = 0.002). The outcome of LTML was slightly improved compared to HDCT (n = 13, EFS 35%, OS 34%). In conclusion, our data suggest that in patients suffering from metastatic RMS, long-term maintenance therapy is a superior strategy in terms of EFS and OS compared to alloHSCT. EFS and OS of HDCT are similar in these strategies; however, the therapeutic burden of LTMT is much lower.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine 04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine > Paediatric Haematology/Oncology |
UniBE Contributor: |
Dantonello, Tobias |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
2072-6694 |
Publisher: |
MDPI AG |
Language: |
English |
Submitter: |
Pubmed Import |
Date Deposited: |
14 Apr 2023 10:27 |
Last Modified: |
11 Jan 2024 12:40 |
Publisher DOI: |
10.3390/cancers15072050 |
PubMed ID: |
37046711 |
Uncontrolled Keywords: |
children long-term maintenance therapy metastatic outcome rhabdomyosarcoma soft tissue sarcoma |
BORIS DOI: |
10.48350/181711 |
URI: |
https://boris.unibe.ch/id/eprint/181711 |