Upfront rational therapy in BRAF V600E mutated pediatric ameloblastoma promotes ad integrum mandibular regeneration.


Journal

Journal of tissue engineering and regenerative medicine
ISSN: 1932-7005
Titre abrégé: J Tissue Eng Regen Med
Pays: England
ID NLM: 101308490

Informations de publication

Date de publication:
12 2021
Historique:
revised: 22 09 2021
received: 25 02 2021
accepted: 25 09 2021
pubmed: 3 10 2021
medline: 22 3 2022
entrez: 2 10 2021
Statut: ppublish

Résumé

Ameloblastoma is a neoplasm arising in the craniofacial skeleton. Proliferating odontogenic epithelial cells comprise this benign, yet locally invasive tumor, often causing severe disfiguration. High recurrence rate entails ablative surgical resection, which is the current standard of care, resulting in subsequent critical size osteocutaneous defects. The high incidence of BRAF mutations in ameloblastoma, most notably the BRAF V600E mutation, enabled the use of BRAF inhibiting agent in a neoadjuvant setting. In this investigator-initiated, open-label study, three consecutive pediatric patients, with confirmed BRAF V600E ameloblastoma deemed marginally resectable, were treated with BRAF inhibiting agents, prior to undergoing surgery. The use of upfront BRAF inhibitor treatment resulted in substantial tumor regression, allowing for non-mutilating complete surgical removal, ad integrum bone regeneration and organ preservation. All patients showed a marked radiologic and clinical response to medical treatment, enabling successful conservative surgery. Microscopically, all patients showed evidence of minimal residual tumor with extensive tumor necrosis, fibrosis and generation of new bone. At a median follow-up of 31 months, all patients remained free of disease. Face preservation therapy was achieved in pediatric patients presenting with BRAF V600E mutated ameloblastoma. Our study demonstrates the translational potential of targeted therapy as a neoadjuvant agent. Patient-specific organ preservation therapy should be considered as the new standard of care in ameloblastoma, mainly for children and adolescents.

Identifiants

pubmed: 34599642
doi: 10.1002/term.3254
doi:

Substances chimiques

BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1155-1161

Informations de copyright

© 2021 John Wiley & Sons Ltd.

Références

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Auteurs

Ariel Hirschhorn (A)

Department of Cranio-Maxillofacial Surgery, Sheba Medical Center, Tel Hashomer, Israel.

Gadi Abebe Campino (GA)

Division of Pediatric Hemato-Oncology, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.

Marilena Vered (M)

Institute of Pathology, Sheba Medical Center, Tel Hashomer, Israel.
Department of Oral Pathology, Oral Medicine and Maxillofacial Imaging, Maurice and Gabriela Goldschleger School of Dental Medicine, Tel Aviv University, Tel Aviv, Israel.

Gahl Greenberg (G)

Department of Radiology, Division of Neuroradiology, Sheba Medical Center, Tel Hashomer, Israel.

Rinat Yacobi (R)

Institute of Pathology, Sheba Medical Center, Tel Hashomer, Israel.

Ran Yahalom (R)

Department of Cranio-Maxillofacial Surgery, Sheba Medical Center, Tel Hashomer, Israel.

Iris Barshack (I)

Institute of Pathology, Sheba Medical Center, Tel Hashomer, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Amos Toren (A)

Division of Pediatric Hemato-Oncology, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ninette Amariglio (N)

Sheba Cancer Research Center, Wohl Institute of Translational Medicine, Sheba Medical Center, Tel Hashomer, Israel.

Gideon Rechavi (G)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Sheba Cancer Research Center, Wohl Institute of Translational Medicine, Sheba Medical Center, Tel Hashomer, Israel.

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