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Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer.

Publication ,  Journal Article
Howell, GM; Carty, SE; Armstrong, MJ; Lebeau, SO; Hodak, SP; Coyne, C; Stang, MT; McCoy, KL; Nikiforova, MN; Nikiforov, YE; Yip, L
Published in: Ann Surg Oncol
December 2011

PURPOSE: This study was designed to examine the aggressive features of BRAF-positive papillary thyroid cancer (PTC) and association with age. METHODS: We compared the clinicopathologic parameters and BRAF V600E mutation status of 121 elderly (age ≥65 years) PTC patients who underwent thyroidectomy from January 2007 to December 2009 to a consecutive cohort of 98 younger (age <65 years) PTC patients. RESULTS: Younger and elderly PTC patients had similar incidences of BRAF-positive tumors (41% vs. 38%; p = 0.67). The elderly cohort was more likely to have smaller tumors (mean 1.6 vs. 2.1 cm; p = 0.001), present with advanced TNM stage (36% vs. 19%; p = 0.008), and have persistent/recurrent disease (10% vs. 1%; p = 0.006). BRAF-positive status was associated with PTC that were tall cell variant (p < 0.001), had extrathyroidal extension (p < 0.001), lymph node involvement (p = 0.008), advanced (III/IV) TNM stage (p < 0.001), and disease recurrence (p < 0.001). Except for lymph node involvement, the association between aggressive histology characteristics at presentation and BRAF-positive PTC also was observed within the age-defined cohorts. In short-term follow-up (mean, 18 months), persistent/recurrent PTC was much more likely to occur in patients who were both BRAF-positive and elderly (22%). CONCLUSIONS: BRAF mutations are equally present in younger and older patients. Aggressive histology characteristics at presentation are associated with BRAF-positive PTC, irrespective of age. However, the well-established association of BRAF with recurrence is limited to older (age ≥65 years) patients.

Duke Scholars

Published In

Ann Surg Oncol

DOI

EISSN

1534-4681

Publication Date

December 2011

Volume

18

Issue

13

Start / End Page

3566 / 3571

Location

United States

Related Subject Headings

  • Young Adult
  • Thyroid Neoplasms
  • Survival Rate
  • Risk Factors
  • Retrospective Studies
  • Proto-Oncogene Proteins B-raf
  • Prognosis
  • Polymerase Chain Reaction
  • Point Mutation
  • Oncology & Carcinogenesis
 

Citation

APA
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ICMJE
MLA
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Howell, G. M., Carty, S. E., Armstrong, M. J., Lebeau, S. O., Hodak, S. P., Coyne, C., … Yip, L. (2011). Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer. Ann Surg Oncol, 18(13), 3566–3571. https://doi.org/10.1245/s10434-011-1781-5
Howell, Gina M., Sally E. Carty, Michaele J. Armstrong, Shane O. Lebeau, Steven P. Hodak, Christopher Coyne, Michael T. Stang, et al. “Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer.Ann Surg Oncol 18, no. 13 (December 2011): 3566–71. https://doi.org/10.1245/s10434-011-1781-5.
Howell GM, Carty SE, Armstrong MJ, Lebeau SO, Hodak SP, Coyne C, et al. Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer. Ann Surg Oncol. 2011 Dec;18(13):3566–71.
Howell, Gina M., et al. “Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer.Ann Surg Oncol, vol. 18, no. 13, Dec. 2011, pp. 3566–71. Pubmed, doi:10.1245/s10434-011-1781-5.
Howell GM, Carty SE, Armstrong MJ, Lebeau SO, Hodak SP, Coyne C, Stang MT, McCoy KL, Nikiforova MN, Nikiforov YE, Yip L. Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer. Ann Surg Oncol. 2011 Dec;18(13):3566–3571.
Journal cover image

Published In

Ann Surg Oncol

DOI

EISSN

1534-4681

Publication Date

December 2011

Volume

18

Issue

13

Start / End Page

3566 / 3571

Location

United States

Related Subject Headings

  • Young Adult
  • Thyroid Neoplasms
  • Survival Rate
  • Risk Factors
  • Retrospective Studies
  • Proto-Oncogene Proteins B-raf
  • Prognosis
  • Polymerase Chain Reaction
  • Point Mutation
  • Oncology & Carcinogenesis