Extracranial germ cell tumours in children and adolescents: Results from the French TGM13 protocol.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
03 2023
Historique:
revised: 02 11 2022
received: 01 08 2022
accepted: 03 11 2022
pubmed: 2 12 2022
medline: 27 1 2023
entrez: 1 12 2022
Statut: ppublish

Résumé

Chemotherapy for non-seminomatous germ cell tumours (NSGCT) exposes to dose-dependent toxicities. The TGM13-NS protocol (EudraCT 2013-004039-60) aimed to decrease the chemotherapy burden compared to the previous TGM95 protocol while maintaining the 5-year event-free survival (EFS) at 80% or more. Patients less than 19 years of age with disseminated NSGCT were enrolled (May 2014 to May 2019) and stratified into four groups: two intermediate-risk (IR: localised tumour with low tumour markers [TM]) groups treated with VBP (vinblastine-bleomycin-cisplatin): three courses for IR1 (ovarian tumour any age/testis tumour less than or equal to 10 years) and four courses for IR2 (extragonadal tumour 10 years or less) groups, and two high-risk (HR: metastatic and/or high TM) groups treated with etoposide-cisplatin and either ifosfamide (VIP) or bleomycin (BEP): three courses for HR1 (ovarian tumour any age/testis tumour less than or equal to 10 years and low TM/testis tumour more than 10 years and very low TM) groups and four courses for HR2 (remainder) groups. One hundred fifteen patients were included: median age of 12.8 years (0.4-18.9); tumour sites: 44 ovaries, 37 testes and 34 extragonadal. The 5-year EFS and overall survival (OS) were 87% (95% CI: 80-92) and 95% (89-98), respectively (median follow-up: 3.5 years, range: 0.2-5.9), similar to those of the TGM95 protocol (5-year EFS 89% (84-93), 5-year OS 93% (89-95), p = .561). The 5-year EFS were 93% (95% CI: 80-98), 88% (71-95) and 79% (62-90) for ovarian, testicular and extragonadal tumours, respectively. The 5-year EFS varied (p = .02) according to the risk groups: 90% (66-97), 64% (30-85), 95% (72-99) and 87% (74-94) for IR1, IR2, HR1 and HR2, respectively. TM decline adjusted to tumour site, and alpha-fetoprotein (AFP) level revealed a prognostic impact of time to normalisation on EFS: HR = 1.03 (1.003-1.007). Risk-adapted and globally decreased chemotherapy burden maintains excellent outcomes, exclusive of the IR2 group, which warrants more intensive chemotherapy.

Sections du résumé

BACKGROUND
Chemotherapy for non-seminomatous germ cell tumours (NSGCT) exposes to dose-dependent toxicities. The TGM13-NS protocol (EudraCT 2013-004039-60) aimed to decrease the chemotherapy burden compared to the previous TGM95 protocol while maintaining the 5-year event-free survival (EFS) at 80% or more.
PROCEDURE
Patients less than 19 years of age with disseminated NSGCT were enrolled (May 2014 to May 2019) and stratified into four groups: two intermediate-risk (IR: localised tumour with low tumour markers [TM]) groups treated with VBP (vinblastine-bleomycin-cisplatin): three courses for IR1 (ovarian tumour any age/testis tumour less than or equal to 10 years) and four courses for IR2 (extragonadal tumour 10 years or less) groups, and two high-risk (HR: metastatic and/or high TM) groups treated with etoposide-cisplatin and either ifosfamide (VIP) or bleomycin (BEP): three courses for HR1 (ovarian tumour any age/testis tumour less than or equal to 10 years and low TM/testis tumour more than 10 years and very low TM) groups and four courses for HR2 (remainder) groups.
RESULTS
One hundred fifteen patients were included: median age of 12.8 years (0.4-18.9); tumour sites: 44 ovaries, 37 testes and 34 extragonadal. The 5-year EFS and overall survival (OS) were 87% (95% CI: 80-92) and 95% (89-98), respectively (median follow-up: 3.5 years, range: 0.2-5.9), similar to those of the TGM95 protocol (5-year EFS 89% (84-93), 5-year OS 93% (89-95), p = .561). The 5-year EFS were 93% (95% CI: 80-98), 88% (71-95) and 79% (62-90) for ovarian, testicular and extragonadal tumours, respectively. The 5-year EFS varied (p = .02) according to the risk groups: 90% (66-97), 64% (30-85), 95% (72-99) and 87% (74-94) for IR1, IR2, HR1 and HR2, respectively. TM decline adjusted to tumour site, and alpha-fetoprotein (AFP) level revealed a prognostic impact of time to normalisation on EFS: HR = 1.03 (1.003-1.007).
CONCLUSION
Risk-adapted and globally decreased chemotherapy burden maintains excellent outcomes, exclusive of the IR2 group, which warrants more intensive chemotherapy.

Identifiants

pubmed: 36451268
doi: 10.1002/pbc.30117
doi:

Substances chimiques

Cisplatin Q20Q21Q62J
Etoposide 6PLQ3CP4P3
Bleomycin 11056-06-7
Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e30117

Informations de copyright

© 2022 The Authors. Pediatric Blood & Cancer published by Wiley Periodicals LLC.

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Auteurs

Cecile Faure-Conter (C)

Department of Pediatric Oncology, Institut d'Hemato-oncologie Pediatrique, Lyon, France.

Daniel Orbach (D)

SIREDO Oncology Center (Care, Innovation and Research for Children, Adolescents and young Adults with Cancer) Institut Curie, PSL University, Paris, France.

Hélène Sudour-Bonnange (H)

Pediatric and Adolescents Oncology Unit, Anti-Cancer Center Oscar Lambret, Lille, France.

Cecile Verité (C)

Pediatric Hematology-Oncology Unit, Pellegrin Hospital, CHU Bordeaux, Bordeaux, France.

Ludovic Mansuy (L)

CHU de Nancy-Hôpital de Brabois, Service d'hémato-oncologie pédiatrique, Vandoeuvre-lès-Nancy Cedex, Nancy, France.

Angelique Rome (A)

Department of Pediatric Oncology, Timone Children's Hospital., Marseille, France.

Cecile Dumesnil (C)

Department of Pediatric Oncology, University Hospital Center of Rouen., Rouen, France.

Estelle Thebaud (E)

Department of Pediatric Oncology, University Hospital Center of Nantes., Nantes, France.

Marleen Renard (M)

Department of Paediatric Hemato-oncology, University Hospital Leuven, Belgium.

Frederic Hameury (F)

Department of Pediatric Surgery, Hôpital Femme Mère Enfant, Lyon, France.

Aude Flechon (A)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Ellen Blanc (E)

Department of Clinical Research and Innovation, Centre Léon Bérard, Lyon, France.

Frederique Dijoud (F)

CHU de Lyon, Institut Multisite de Pathologie, France.

Brice Fresneau (B)

Department of Children and Adolescent Oncology, Gustave Roussy, Université Paris-Saclay, Paris-Saclay University, Paris-Sud University, CESP, INSERM, Villejuif, France.

Sylvie Chabaud (S)

Statistical Unit, Clinical Research Department, Centre Léon Bérard, Lyon, France.

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