Microscopically positive resection margin after hepatoblastoma resection: what is the impact on prognosis? A Childhood Liver Tumours Strategy Group (SIOPEL) report.


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:
01 2019
Historique:
received: 14 06 2018
revised: 08 10 2018
accepted: 22 10 2018
pubmed: 12 12 2018
medline: 6 5 2020
entrez: 12 12 2018
Statut: ppublish

Résumé

To evaluate the impact of a microscopically positive resection margin (microPRM) on the outcome of hepatoblastoma patients pretreated with chemotherapy. Local recurrence and survival rates of 431 children treated in the SIOPEL 2 and 3 trials were analysed comparing 58 patients with microPRM with 371 who had a complete resection (CR) and who were then stratified by risk category. The tumour was standard-risk in 312 patients and high-risk (PRETEXT IV and/or extrahepatic disease and/or α-fetoprotein [AFP]<100 ng/ml) in 117 patients. All received cisplatinum-based neoadjuvant and postoperative chemotherapy as per protocol. Apart from one microPRM patient who went on to transplant, none received any additional local treatment. With a median follow-up of 67 months, local relapse occurred in 3/58 patients with microPRM (5%) and in 23/371 (6%) patients with CR. The 5-year overall survival (OS) was 91% (95% confidence interval [CI] 80%-96%) for the microPRM and 92% (95% CI 89%-95%) for the CR group. The 5-year event-free survival (EFS) was 86% (95% CI 74%-93%) for the microPRM and 86% (95% CI 82%-89%) for the CR group. Neither OS nor EFS was statistically significantly different between the two groups, neither overall nor when risk group stratified. In the context of cisplatin-based chemotherapy, the presence of microPRM did not influence the outcome even without additional local treatment. Although CR remains the aim, microPRM does not necessitate mandatory second look surgery. A 'wait and see policy' is warranted if postoperative chemotherapy is administered and AFP levels and imaging become normal.

Sections du résumé

BACKGROUND
To evaluate the impact of a microscopically positive resection margin (microPRM) on the outcome of hepatoblastoma patients pretreated with chemotherapy.
METHODS
Local recurrence and survival rates of 431 children treated in the SIOPEL 2 and 3 trials were analysed comparing 58 patients with microPRM with 371 who had a complete resection (CR) and who were then stratified by risk category. The tumour was standard-risk in 312 patients and high-risk (PRETEXT IV and/or extrahepatic disease and/or α-fetoprotein [AFP]<100 ng/ml) in 117 patients. All received cisplatinum-based neoadjuvant and postoperative chemotherapy as per protocol. Apart from one microPRM patient who went on to transplant, none received any additional local treatment.
RESULTS
With a median follow-up of 67 months, local relapse occurred in 3/58 patients with microPRM (5%) and in 23/371 (6%) patients with CR. The 5-year overall survival (OS) was 91% (95% confidence interval [CI] 80%-96%) for the microPRM and 92% (95% CI 89%-95%) for the CR group. The 5-year event-free survival (EFS) was 86% (95% CI 74%-93%) for the microPRM and 86% (95% CI 82%-89%) for the CR group. Neither OS nor EFS was statistically significantly different between the two groups, neither overall nor when risk group stratified.
CONCLUSIONS
In the context of cisplatin-based chemotherapy, the presence of microPRM did not influence the outcome even without additional local treatment. Although CR remains the aim, microPRM does not necessitate mandatory second look surgery. A 'wait and see policy' is warranted if postoperative chemotherapy is administered and AFP levels and imaging become normal.

Identifiants

pubmed: 30528797
pii: S0959-8049(18)31452-7
doi: 10.1016/j.ejca.2018.10.013
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

126-132

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Daniel C Aronson (DC)

Department of Paediatric Surgery, University Children`s Hospital Zürich, Zürich, Switzerland. Electronic address: dan.aronson@kispi.uzh.ch.

Víola B Weeda (VB)

Department of Surgery, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.

Rudolf Maibach (R)

IBCSG Coordinating Center, Berne, Switzerland.

Piotr Czauderna (P)

Department of Surgery and Urology for Children and Adolescents, Medical University of Gdansk, Gdansk, Poland.

Patrizia Dall'Igna (P)

Department of Pediatric Surgery, University Hospital of Padua, Padua, Italy.

Jean de Ville de Goyet (J)

Department of Pediatric Surgery and Transplantation, ISMETT - UPMC, Palermo, Sicile, Italy.

Sophie Branchereau (S)

Dept. of Pediatric Surgery, APHP Bicêtre Hospital, Le Kremlin-Bicetre, Paris, France.

Giorgio Perilongo (G)

Department of Pediatrics, University Hospital of Padua, Padua, Italy.

Penelope Brock (P)

Department of Pediatrics, Great Ormond Street Hospital for Children, London, United Kingdom.

Joszef Zsiros (J)

Department of Pediatric Oncology, Máxima Medisch Centrum, Utrecht, the Netherlands.

Michaela Semeraro (M)

Clinical Research Unit, Paris Centre Necker-Cochin, APHP, Paris, France.

Christophe Chardot (C)

Department of Pediatric Surgery, Hopital Universaire Necker Enfants Malade, Paris, France.

Barbara Wildhaber (B)

Department of Pediatric Surgery, Hopiteau Universitaires de Geneve, Geneve, Switzerland.

Bruce Morland (B)

Department of Paediatric Oncology, Birmingham Children's Hospital, Birmingham, United Kingdom.

Laurence Brugières (L)

Department of Children and Adolescents Oncology, Gustave Roussy, Villejuif, Paris, France.

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