Outcome of patients with undifferentiated embryonal sarcoma of the liver treated according to European soft tissue sarcoma protocols

Author:

Guérin Florent1ORCID,Martelli Hélène1,Rogers Timothy2ORCID,Zanetti Ilaria3,van Scheltinga Sheila Terwisscha4,De Corti Federica5,Burrieza Gabriella Guillen6,Minard‐Colin Véronique7,Orbach Daniel8ORCID,van Noesel Max M.4ORCID,Karanian Marie9,Fajardo Raquel Dávila10ORCID,Merks Johannes H. M.4,Ferrari Andrea11ORCID,Bisogno Gianni3ORCID

Affiliation:

1. Department of Pediatric Surgery Université Paris‐Saclay Assistance Publique Hôpitaux de Paris (AP‐HP) Bicêtre Hospital Le Kremlin Bicêtre France

2. Department of Pediatric Surgery University Hospitals Bristol and Weston NHS foundation trust Bristol UK

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

4. Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands

5. Department of Women's and Children's Health Pediatric Surgery Unit University of Padova Padua Italy

6. Department of Pediatric Surgery Vall d'Hebron University Hospital Barcelona Spain

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

8. SIREDO Oncology Center (Care, Innovation and Research for Children, Adolescents and Young Adults with Cancer) Paris Science et Lettres University Institut Curie Paris France

9. Department of Biopathology UNICANCER Centre Leon Bérard Lyon France

10. Department of Radiation Oncology University Medical Center Utrecht Utrecht The Netherlands

11. Pediatric Oncology Unit Fondazione IRCCS Istituto Nazionale dei Tumori Milan Italy

Abstract

AbstractBackgroundTo assess the outcomes of pediatric patients with undifferentiated embryonal sarcoma of the liver (UESL) and treatment including at least surgery and systemic chemotherapy.MethodsThis study included patients aged up to 21 years with a pathological diagnosis of UESL prospectively enrolled from 1995 to 2016 in three European trials focusing on the effects of surgical margins, preoperative chemotherapy, use of radiotherapy (RT), and chemotherapy.ResultsOut of 65 patients with a median age at diagnosis of 8.7 years (0.6–20.8), 15 had T2 tumors, and one had lymph node spread, 14 were Intergroup Rhabdomyosarcoma Study (IRS) I, nine IRS II, 38 IRS III, and four IRS IV. Twenty‐eight upfront surgeries resulted in five operative spillages and 11 infiltrated surgical margins, whereas 37 delayed surgeries resulted in no spillages (p = .0119) and three infiltrated margins (p = .0238). All patients received chemotherapy, including anthracyclines in 47. RT was administered in 15 patients. With a median follow‐up of 78.6 months, 5‐year overall and event‐free survivals (EFS) were 90.1% (95% confidence interval [CI]: 79.2–95.5) and 89.1% (95% CI: 78.4–94.6), respectively. Two out four local relapses had previous infiltrated margins and two out of three patients with metastatic relapses received reduced doses of alkylating agents. Infiltrated margins (p = .1607), T2 stage (p = .3870), use of RT (p = .8731), and anthracycline‐based chemotherapy (p = .1181) were not correlated with EFS.ConclusionsMultimodal therapy improved the outcome of UESL. Neoadjuvant chemotherapy for pediatric patients increases the probability of complete surgical resection. The role of anthracyclines and RT for localized disease remains unclear.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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