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Non-parameningeal head and neck rhabdomyosarcoma in children, adolescents, and young adults: Experience of the European paediatric Soft tissue sarcoma Study Group (EpSSG) - RMS2005 study.
Glosli, Heidi; Bisogno, Gianni; Kelsey, Anna; Chisholm, Julia C; Gaze, Mark; Kolb, Frederic; McHugh, Kieran; Shipley, Janet; Gallego, Soledad; Merks, Johannes H M; Smeele, Ludi E; Mandeville, Henry; Ferrari, Andrea; Minard-Colin, Veronique; Corradini, Nadege; Jenney, Meriel; Zanetti, Ilaria; De Salvo, Gian L; Orbach, Daniel.
Afiliação
  • Glosli H; Paediatric Research Institute, Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway. Electronic address: hglosli@ous-hf.no.
  • Bisogno G; Hematology Oncology Division, Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Kelsey A; Department of Paediatric Histopathology, Royal Manchester Children's Hospital, Manchester, United Kingdom.
  • Chisholm JC; Children and Young Peoples Unit, Royal Marsden Hospital, Down's Road, Sutton, Surrey SM2 5PT, United Kingdom.
  • Gaze M; Department of Oncology, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Kolb F; Department of Plastic Surgery, Gustave Roussy Cancer Campus, Villejuif, France; Department of Plastic Surgery, UCSD, San Diego, CA, USA.
  • McHugh K; Department of Radiology, Great Ormond Street Hospital for Children, London, United Kingdom.
  • Shipley J; The Institute of Cancer Research, Sutton, United Kingdom.
  • Gallego S; Paediatric Oncology, Hospital Universitari Vall D'Hebron, Barcelona, Spain.
  • Merks JHM; Princess Máxima Center for Paediatric Oncology, Utrecht, the Netherlands.
  • Smeele LE; Department of Head and Neck Oncology and Surgery, Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Amsterdam, the Netherlands; Department of Oral and Maxillofacial Surgery, Amsterdam UMC, Amsterdam, the Netherlands; Solid Tumor Department, Princess Máxima Center for Paediatric Oncology,
  • Mandeville H; Children and Young Peoples Unit & Haemato-oncology Unit, Royal Marsden Hospital, NHS Foundation Trust, Sutton, United Kingdom.
  • Ferrari A; Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
  • Minard-Colin V; Department of Pediatric and Adolescent Oncology, INSERM, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Corradini N; Paediatric Hematology and Oncology Institute, Léon Bérard Center, Lyon, France.
  • Jenney M; Department of Paediatric Oncology, Children's Hospital for Wales, Heath Park, Cardiff, United Kingdom.
  • Zanetti I; Hematology Oncology Division, Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • De Salvo GL; Clinical Trials and Biostatistics Unit, Istituto Oncologico Veneto - IRCCS, Padova, Italy.
  • Orbach D; SIREDO Oncology Center, Institute Curie, PSL University, Paris, France.
Eur J Cancer ; 151: 84-93, 2021 07.
Article em En | MEDLINE | ID: mdl-33971448
ABSTRACT
BACKGROUND/

OBJECTIVES:

The primary aim of this study was to analyse and evaluate the impact of different local treatments on the pattern of relapse in children with primary head and neck non-parameningeal (HNnPM) rhabdomyosarcoma (RMS), treated in the European paediatric Soft tissue sarcoma Study Group (EpSSG) RMS2005 study. The secondary aim was to assess whether current risk stratification is valid for this specific site. DESIGN/

METHODS:

This study includes all patients with localised HNnPM RMS enrolled in the RMS2005 study between 2005 and 2016. Treatment comprised chemotherapy adapted to risk group, with local surgery and/or radiation therapy. The main outcome measures were event-free survival (EFS) and overall survival (OS).

RESULTS:

A total of 165 patients were identified; the median age was 6.4 years (range, 0.1-25). The most common tumour sites were cheek/chin (22%) and nasal ala/nasolabial fold (20%). Histology was unfavourable for 40%, and regional nodal involvement present in 26%. Local therapy included surgery (58%) and/or radiotherapy (72%) to primary tumour and/or regional lymph nodes. After a median follow-up of 66 months (range, 6-158), 42 patients experienced an event, and 17 are still alive. Tumour events were frequent in oral primary (36%), parotid site (26%), cheek/chin (24%), and nasal ala/nasolabial fold (24%) and included locoregional failure in 84% of cases. The 5-year EFS and OS were 75% (95% confidence interval [CI] 67.3-81.2) and 84.9% (95% CI 77.5-89.7), respectively. Favourable histology was associated with a better EFS (82.3% versus 64.6%; p = 0.02) and nodal spread with a worse OS (88.6% versus 76.1%; p = 0.04). Different sublocations within the HNnPM primary did not have significant impact on outcome.

CONCLUSION:

Locoregional relapse/progression is the main tumour failure event in this site. Despite frequent unfavourable risk factors, HNnPM RMS remains a favourable location in the context of a risk-adapted strategy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rabdomiossarcoma / Neoplasias de Cabeça e Pescoço / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: America do sul / Argentina / Asia / Brasil / Europa Idioma: En Revista: Eur J Cancer Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rabdomiossarcoma / Neoplasias de Cabeça e Pescoço / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: America do sul / Argentina / Asia / Brasil / Europa Idioma: En Revista: Eur J Cancer Ano de publicação: 2021 Tipo de documento: Article