Metastatic adult‐type non‐rhabdomyosarcoma soft tissue sarcomas in children and adolescents: A cohort study from the European paediatric Soft tissue sarcoma Study Group

Author:

Ferrari Andrea1ORCID,Orbach Daniel2ORCID,Casanova Michela1,van Noesel Max M.3,Berlanga Pablo4,Brennan Bernadette5,Corradini Nadege6,Schoot Reineke A.3,Ramirez‐Villar Gema L.7,Hjalgrim Lisa Lyngsie8,Alaggio Rita9,Guillen Burrieza Gabriela10,Safwat Akmal11,Cameron Alison L.12,van Rijn Rick R.13,Minard‐Colin Veronique4ORCID,Zanetti Ilaria14,Bisogno Gianni1415ORCID,Chisholm Julia C.16,Merks Johannes H. M.317

Affiliation:

1. Pediatric Oncology Unit Fondazione IRCCS Istituto Nazionale Tumori Milano Italy

2. SIREDO Oncology Center Institut Curie PSL University Paris France

3. Princess Máxima Center for Pediatric Oncology Utrecht Netherlands

4. Department of Pediatric and Adolescent Oncology Gustave‐Roussy Cancer Campus Université Paris‐Saclay Villejuif France

5. Pediatric Oncology Royal Manchester Children's Hospital Manchester UK

6. Department of Pediatric Oncology Institut d’Hematologie et d’Oncologie Pédiatrique,/Centre Léon Bérard Lyon France

7. Pediatric Oncology Unit Hospital Universitario Virgen del Rocío Sevilla Spain

8. Department of Pediatrics and Adolescent Medicine Rigshospitalet University of Copenhagen Copenhagen Denmark

9. Pathology Department Ospedale Pediatrico Bambino Gesù IRCCS Rome Italy

10. Surgical Oncology and Neonatal Surgery Pediatric Surgery Department Hospital Infantil Universitari Vall d’Hebron Barcelona Spain

11. Oncology Department and Danish Center for Particle Therapy Aarhus University Hospital Aarhus Denmark

12. Bristol Haematology and Oncology Centre University Hospitals Bristol and Weston NHS Foundation Trust Bristol UK

13. Department of Radiology and Nuclear Medicine UMC University of Amsterdam Amsterdam Netherlands

14. Pediatric Hematology Oncology Division University Hospital of Padua Padua Italy

15. Department of Women's and Children's Health University of Padua Padua Italy

16. Children and Young People's Unit The Royal Marsden Hospital and Institute of Cancer Research Sutton UK

17. Division of Imaging and Oncology University Medical Center Utrecht Utrecht University Utrecht The Netherlands

Abstract

AbstractBackgroundLimited data exist on the clinical behavior of pediatric non‐rhabdomyosarcoma soft tissue sarcomas (NRSTS) with distant metastases at onset, and a clear standard of care has not yet been defined.MethodsThis cohort study reports on pediatric adult‐type metastatic NRSTS enrolled in two concurrent prospective European studies, i.e., the randomized BERNIE study and the single‐arm MTS 2008 study developed by the European paediatric Soft tissue sarcoma Study Group. Treatment programs were originally designed for patients with metastatic rhabdomyosarcoma, i.e., nine courses of multidrug chemotherapy (with or without bevacizumab in the BERNIE study), followed by 12 cycles of maintenance therapy, whereas radiotherapy and/or surgery (on primary tumor and/or metastases) were delayed until after seven courses of chemotherapy had been administered.ResultsThe study included 61 patients <21 years old treated from July 2008 to December 2016. The lung was the site of metastases in 75% of the cases. All patients received multi‐agent chemotherapy, 44% had local therapy to primary tumor, and 18% had treatment of metastases. Median time to progression/relapse was 6 months. A high rate of tumor progression was observed during the initial part of the chemotherapy program. With a median follow‐up of 41.5 months (range, 2–111 months), 3‐year event‐free survival and overall survival were 15.4% (95% confidence interval [CI], 7.6–25.7) and 34.9% (95% CI, 22.7–47.5), respectively. There were no statistically significant differences in outcome depending on the type of treatment administered.ConclusionsThe study confirmed the overall poor outcome for patients with metastatic NRSTS, whose treatment remains a challenge.Plain Language Summary Pediatric non‐rhabdomyosarcoma soft tissue sarcomas form a heterogeneous group of rare tumors. Although recent international studies have defined the standard of care for patients with localized disease, limited data are available on the clinical behavior of patients with distant metastases. This study on 61 metastatic cases treated on two prospective European protocols confirms that the chances of survival of such patients are often dismal and a standard treatment is still lacking.

Publisher

Wiley

Subject

Cancer Research,Oncology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3