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

被引:28
|
作者
Glosli, Heidi [1 ]
Bisogno, Gianni [2 ]
Kelsey, Anna [3 ]
Chisholm, Julia C. [4 ]
Gaze, Mark [5 ]
Kolb, Frederic [6 ,7 ]
McHugh, Kieran [8 ]
Shipley, Janet [9 ]
Gallego, Soledad [10 ]
Merks, Johannes H. M. [11 ]
Smeele, Ludi E. [12 ,13 ,14 ]
Mandeville, Henry [15 ,16 ]
Ferrari, Andrea [17 ]
Minard-Colin, Veronique [18 ]
Corradini, Nadege [19 ]
Jenney, Meriel [20 ]
Zanetti, Ilaria [2 ]
De Salvo, Gian L. [21 ]
Orbach, Daniel [22 ]
机构
[1] Oslo Univ Hosp, Paediat Res Inst, Div Paediat & Adolescent Med, Oslo, Norway
[2] Univ Padua, Dept Womens & Childrens Hlth, Hematol Oncol Div, Padua, Italy
[3] Royal Manchester Childrens Hosp, Dept Paediat Histopathol, Manchester, Lancs, England
[4] Royal Marsden Hosp, Children & Young Peoples Unit, Downs Rd, Sutton SM2 5PT, Surrey, England
[5] Univ Coll London Hosp NHS Fdn Trust, Dept Oncol, London, England
[6] Gustave Roussy Canc Campus, Dept Plast Surg, Villejuif, France
[7] Univ Calif San Diego, Dept Plast Surg, San Diego, CA USA
[8] Great Ormond St Hosp Sick Children, Dept Radiol, London, England
[9] Inst Canc Res, Sutton, Surrey, England
[10] Hosp Univ Vall DHebron, Paediat Oncol, Barcelona, Spain
[11] Princess Maxima Ctr Paediat Oncol, Utrecht, Netherlands
[12] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Head & Neck Oncol & Surg, Amsterdam, Netherlands
[13] Amsterdam UMC, Dept Oral & Maxillofacial Surg, Amsterdam, Netherlands
[14] Princess Maxima Ctr Paediat Oncol, Solid Tumor Dept, Utrecht, Netherlands
[15] NHS Fdn Trust, Royal Marsden Hosp, Children & Young Peoples Unit, Sutton, Surrey, England
[16] NHS Fdn Trust, Royal Marsden Hosp, Haematooncol Unit, Sutton, Surrey, England
[17] Fdn IRCCS Ist Nazl Tumori, Pediat Oncol Unit, Milan, Italy
[18] Univ Paris Saclay, Dept Pediat & Adolescent Oncol, INSERM, Gustave Roussy, Villejuif, France
[19] Leon Berard Ctr, Paediat Hematol & Oncol Inst, Lyon, France
[20] Childrens Hosp Wales, Dept Paediat Oncol, Heath Pk, Cardiff, Wales
[21] Ist Oncol Veneto IRCCS, Clin Trials & Biostat Unit, Padua, Italy
[22] PSL Univ, SIREDO Oncol Ctr, Inst Curie, Paris, France
关键词
Rhabdomyosarcoma; Head and neck non-parameningeal primary; Children; Adolescents and young adults; EpSSG; RMS2005; NONMETASTATIC RHABDOMYOSARCOMA; INTERNATIONAL-SOCIETY; INTERGROUP RHABDOMYOSARCOMA; NONPARAMENINGEAL HEAD; CHILDHOOD; ONCOLOGY; TUMORS; RADIOTHERAPY; LESSONS;
D O I
10.1016/j.ejca.2021.04.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (c)& nbsp;2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页码:84 / 93
页数:10
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