Consensus and controversy in the management of paediatric and adult patients with ovarian immature teratoma: the Malignant Germ Cell International Consortium perspective.

Grade Immature teratoma Ovarian Stage

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 25 10 2023
revised: 27 12 2023
accepted: 13 01 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

Ovarian immature teratoma (IT) is a rare neoplasm comprising ∼3% of ovarian cancers, occurring primarily in young females. Management presents several challenges, including those with elevated serum alpha-fetoprotein, potential confusion regarding pathology interpretation, and paucity of data to support decision-making. MaGIC (https://magicconsortium.com/) is an interdisciplinary international consortium of GCT experts from multiple subspecialties, with members receiving frequent queries regarding IT patient management. With evidence from published literature where available, we summarise consensus management of such patients. Given lack of published data, controversy in certain areas remains. The most obvious variance in practice is between paediatric and adult teams, despite very similar outcomes. Paediatric teams typically employ a surgery-only approach, whereas in adult practice, all patients, except those with stage IA, grade 1 (low-grade) tumours, still generally receive adjuvant chemotherapy. Given the rarity of ovarian IT and lack of published data, discussion with GCT experts and/or national advisory panels is recommended.

Identifiants

pubmed: 38544795
doi: 10.1016/j.eclinm.2024.102453
pii: S2589-5370(24)00032-4
pmc: PMC10965411
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

102453

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

The authors have no conflicts to declare.

Auteurs

Farzana Pashankar (F)

Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.

Matthew J Murray (MJ)

Department of Pathology, Tennis Court Road, University of Cambridge, CB2 1QP, UK.
Department of Paediatric Haematology and Oncology, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge, CB2 0QQ, UK.

Joanna Gell (J)

The Center for Cancer and Blood Disorders, Connecticut Children's Medical Center, Hartford, CT, USA.
Department of Pediatrics, University of Connecticut Medical School, Farmington, CT, USA.
The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.

Nicola MacDonald (N)

Department of Gynaecological Surgery, University College Hospital, University College London Hospital, NHS Foundation Trust, London, UK.

Jonathan Shamash (J)

Department of Medical Oncology, St Bartholomew's Hospital, London, W Smithfield, London, EC1A 7BE, UK.

Deborah F Billmire (DF)

Department of Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.

Lindsay Klosterkemper (L)

Harvard Medical School, Boston, MA, USA.
Dana Farber/Boston Children's Cancer and Blood Center, Boston, MA, USA.

Thomas Olson (T)

Department of Pediatrics, Aflac Cancer and Blood Disorders Center, Emory University School of Medicine, Atlanta, GA, USA.

Michelle S Hirsch (MS)

Department of Pathology, Women's and Perinatal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Michelle Lockley (M)

Department of Medical Oncology, University College Hospital, University College London Hospital, NHS Foundation Trust, London, UK.
Centre for Cancer Genomics and Computational Biology, Barts Cancer Institute, Queen Mary University of London, London, UK.

Sara Stoneham (S)

Department of Paediatrics, University College Hospital, University College London Hospital, NHS Foundation Trust, London, UK.

A Lindsay Frazier (AL)

Harvard Medical School, Boston, MA, USA.
Dana Farber/Boston Children's Cancer and Blood Center, Boston, MA, USA.

Classifications MeSH