Do patients with familial nonmedullary thyroid cancer present with more aggressive disease? Implications for initial surgical treatment.


Journal

Surgery
ISSN: 1532-7361
Titre abrégé: Surgery
Pays: United States
ID NLM: 0417347

Informations de publication

Date de publication:
01 2019
Historique:
received: 01 02 2018
revised: 02 04 2018
accepted: 07 05 2018
pubmed: 18 10 2018
medline: 15 10 2019
entrez: 18 10 2018
Statut: ppublish

Résumé

There are conflicting reports on whether familial nonmedullary thyroid cancer is more aggressive than sporadic nonmedullary thyroid cancer. Our aim was to determine if the clinical and pathologic characteristics of familial nonmedullary thyroid cancer are different than nonmedullary thyroid cancer. We compared patients with familial nonmedullary thyroid cancer to a cohort of 53,571 nonmedullary thyroid cancer patients from the Surveillance, Epidemiology, and End Results database. A total of 78 patients with familial nonmedullary thyroid cancer from 31 kindreds presented at a younger age (P = .04) and had a greater rate of T1 disease (P = .019), lymph node metastasis (P = .002), and the classic variant of papillary thyroid cancer on histology (P < .001) compared with the Surveillance, Epidemiology, and End Results cohort. Patients with ≥3 affected family members presented at a younger age (P = .04), had a lesser female-to-male ratio (P = .04), and had a greater rate of lymph node metastasis (P = .009). Compared with the Surveillance, Epidemiology, and End Results cohort, we found a higher prevalence of lymph node metastasis in familial nonmedullary thyroid cancer index cases (P = .003) but not in those diagnosed by screening ultrasonography (P = .58). Patients with familial nonmedullary thyroid cancer present at a younger age and have a greater rate of lymph node metastasis. The treatment for familial nonmedullary thyroid cancer should be more aggressive in patients who present clinically and in those who have ≥3 first-degree relatives affected.

Sections du résumé

BACKGROUND
There are conflicting reports on whether familial nonmedullary thyroid cancer is more aggressive than sporadic nonmedullary thyroid cancer. Our aim was to determine if the clinical and pathologic characteristics of familial nonmedullary thyroid cancer are different than nonmedullary thyroid cancer.
METHODS
We compared patients with familial nonmedullary thyroid cancer to a cohort of 53,571 nonmedullary thyroid cancer patients from the Surveillance, Epidemiology, and End Results database.
RESULTS
A total of 78 patients with familial nonmedullary thyroid cancer from 31 kindreds presented at a younger age (P = .04) and had a greater rate of T1 disease (P = .019), lymph node metastasis (P = .002), and the classic variant of papillary thyroid cancer on histology (P < .001) compared with the Surveillance, Epidemiology, and End Results cohort. Patients with ≥3 affected family members presented at a younger age (P = .04), had a lesser female-to-male ratio (P = .04), and had a greater rate of lymph node metastasis (P = .009). Compared with the Surveillance, Epidemiology, and End Results cohort, we found a higher prevalence of lymph node metastasis in familial nonmedullary thyroid cancer index cases (P = .003) but not in those diagnosed by screening ultrasonography (P = .58).
CONCLUSION
Patients with familial nonmedullary thyroid cancer present at a younger age and have a greater rate of lymph node metastasis. The treatment for familial nonmedullary thyroid cancer should be more aggressive in patients who present clinically and in those who have ≥3 first-degree relatives affected.

Identifiants

pubmed: 30327187
pii: S0039-6060(18)30509-9
doi: 10.1016/j.surg.2018.05.075
pmc: PMC6721606
mid: NIHMS1042037
pii:
doi:

Types de publication

Comparative Study Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

50-57

Subventions

Organisme : Intramural NIH HHS
ID : Z99 DK999999
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

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Auteurs

Mustapha El Lakis (M)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Andreas Giannakou (A)

National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

Pavel J Nockel (PJ)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Douglas Wiseman (D)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Sudheer Kumar Gara (SK)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Dhaval Patel (D)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Zahraa Abdul Sater (ZA)

Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

Yevgeniya Y Kushchayeva (YY)

Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

Joanna Klubo-Gwiezdzinska (J)

Metabolic Disease Branch, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.

Naris Nilubol (N)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Maria J Merino (MJ)

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Electron Kebebew (E)

Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; Stanford University, School of Medicine, Stanford, California. Electronic address: kebebew@stanford.edu.

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Classifications MeSH