External beam radiation therapy for recurrent or residual thyroid cancer: What is the best treatment time and the best candidate for long-term local disease control?

cervical disease external beam radiation radiation therapy thyroid cancer

Journal

Head & neck
ISSN: 1097-0347
Titre abrégé: Head Neck
Pays: United States
ID NLM: 8902541

Informations de publication

Date de publication:
06 Mar 2024
Historique:
revised: 07 02 2024
received: 30 12 2023
accepted: 10 02 2024
medline: 6 3 2024
pubmed: 6 3 2024
entrez: 6 3 2024
Statut: aheadofprint

Résumé

Cervical disease control might be challenging in advanced thyroid cancer (DTC). Indications for cervical external beam radiation therapy (EBRT) are controversial. To identify clinical and molecular factors associated with control of cervical disease with EBRT. Retrospective evaluation and molecular analysis of the primary tumor DTC patients who underwent cervical EBRT between 1995 and 2022 was performed. Eighty adults, median age of 61 years, were included. T4 disease was present in 43.7%, lymph node involvement in 42.5%, and distant metastasis in 47.5%. Those with cervical progression were older (62.5 vs. 57.3, p = 0.04) with more nodes affected (12.1 vs. 2.8, p = 0.04) and had EBRT performed later following surgery (76.6 vs. 64 months, p = 0.05). EBRT associated with multikinase inhibitors showed longer overall survival than EBRT alone (64.3 vs. 37.9, p = 0.018) and better local disease control. Performing EBRT before radioiodine (RAI) was associated with longer cervical progression-free survival (CPFS) than was RAI before (67.5 vs. 34.5, p < 0.01). EBRT ≥2 years after surgery was associated with worse CPFS (4.9 vs. 34, p = 0.04). The most common molecular alterations were ERBB2, BRAF, FAT1, RET and ROS1 and TERT mutation was predictive of worse disease control after EBRT (p = 0.04). Younger patients, with fewer affected nodes and treated earlier after surgery had better cervical disease control. Combination of EBRT with MKI improved OS. TERT mutation might indicate worse responders to EBRT; however, further studies are necessary to clarify the role of molecular testing in selecting candidates for cervical EBRT.

Identifiants

pubmed: 38445804
doi: 10.1002/hed.27702
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
ID : E_10/2016E

Informations de copyright

© 2024 Wiley Periodicals LLC.

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Auteurs

Lara Bessa Campelo Pinheiro Cavalcante (LBCP)

Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Natalia Treistman (N)

Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Fabiola Maria Teresa Torres Gonzalez (FMTT)

Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Pollyanna Iemini Weyll Fernandes (PIW)

Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Paulo Alonso Garcia Alves Junior (PAG)

Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Fernanda Accioly Andrade (FA)

Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Elisa Napolitano Ferreira (EN)

Grupo Fleury, São Paulo, Brazil.

Tarcisio Fontenele De Brito (TF)

Institute of Biomedical Sciences, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Attilio Pane (A)

Institute of Biomedical Sciences, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Rossana Corbo (R)

Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Felipe Erlich (F)

Radiotherapy, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Daniel Alves Bulzico (DA)

Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Fernanda Vaisman (F)

Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Classifications MeSH