Therapy and prognostic significance of regional lymph node involvement in embryonal rhabdomyosarcoma: a report from the European paediatric Soft tissue sarcoma Study Group.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
09 2022
Historique:
received: 25 02 2022
revised: 03 05 2022
accepted: 20 05 2022
pubmed: 29 6 2022
medline: 17 8 2022
entrez: 28 6 2022
Statut: ppublish

Résumé

Regional lymph node disease (N1) is a component of the risk-based treatment stratification in rhabdomyosarcoma (RMS). The purpose of this study was to determine the contribution of nodal disease to the prognosis of patients with non-metastatic embryonal RMS (ERMS) and analyse their outcome by treatment received. Between 2005 and 2016, 1294 children with ERMS were enrolled in the European paediatric Soft tissue sarcoma Study Group (EpSSG) RMS 2005 protocol, 143 patients with N1. Treatment comprised 9 cycles of ifosfamide, vincristine and dactinomycin. Some patients also received doxorubicin and/or maintenance if enrolled in the randomised studies. Local treatment was planned after 4 cycles of chemotherapy and included surgery to remove macroscopic residual tumour and/or radiotherapy (primary tumour and involved nodes). N1 patients were older and presented with tumours of unfavourable size, invasiveness, site and resectability. Unlike alveolar RMS, nodal involvement was more frequent in the head and neck area and rare in extremity sites. The 5-year event-free and overall survival were 75.5% and 86.3% for patients with N0, and 65.2% and 70.7% for patients with N1, respectively. The nodal involvement and the result of surgery at diagnosis (Intergroup Rhabdomyosarcoma Study group) were independent prognostic factors on multivariate analysis. Considering only patients with N1 ERMS, we were not able to identify any treatment variables which correlated with the outcome. In the case of nodal involvement, patients with ERMS present different characteristics and a better outcome than alveolar RMS. Regional nodal involvement is an independent prognostic factor in ERMS, therefore it is appropriate to include this population in the high-risk category.

Identifiants

pubmed: 35763871
pii: S0959-8049(22)00321-5
doi: 10.1016/j.ejca.2022.05.033
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

119-129

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Myriam Ben-Arush (M)

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

Veronique Minard-Colin (V)

Department of Pediatric and Adolescent Oncology, INSERM U1015, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Giovanni Scarzello (G)

Radiotherapy Department, Veneto Institute of Oncology - IOV IRCCS, Padua, Italy.

Raquel D Fajardo (RD)

Department of Radiation Oncology, University Medical Center Utrecht, Utrecht, the Netherlands; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Sheila Terwisscha Van Scheltinga (S)

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Valérie Bernier (V)

Department of Radiation Oncology, Institut de Cancerologie de Lorraine, Vandoeuvre-les- Nancy, France.

Meriel Jenney (M)

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

Soledad Gallego (S)

Pediatric Oncology and Hematology, Children's Hospital Vall D'Hebron, Spain.

Ilaria Zanetti (I)

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

Maja Cesen (M)

Pediatric Hematology and Oncology Department, University Children's Hospital Ljubljana, Slovenia.

Johannes H M Merks (JHM)

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

Gianni Bisogno (G)

Hematology Oncology Division, Department of Women's and Children's Health University of Padova, Padova Italy. Electronic address: gianni.bisogno@unipd.it.

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Classifications MeSH