Outcome after treatment of high-risk papillary and non-Hurthle-cell follicular thyroid carcinoma

Terry Taylor, Bonny Specker, Jacob Robbins, Matthew Sperling, Mona Ho, Kenneth Ain, S. Thomas Bigos, Jim Brierley, David Cooper, Bryan Haugen, Ian Hay, Vicki Hertzberg, Irwin Klein, Herbert Klein, Paul Ladenson, Ronald Nishiyama, Douglas Ross, Steven Sherman, Harry R. Maxon

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149 Scopus citations

Abstract

Background: Treatment of differentiated thyroid cancer has been studied for many years, but the benefits of extensive initial thyroid surgery and the addition of radioiodine therapy or external radiation therapy remain controversial. Objective: To determine the relations among extent of surgery, radioiodine therapy, and external radiation therapy in the treatment of high- risk papillary and non-Hurthle-cell follicular thyroid carcinoma. Design: Analysis of data from a multicenter study. Setting: 14 institutions in the United States and Canada participating in the National Thyroid Cancer Treatment Cooperative Study Registry. Patients: 385 patients with high-risk thyroid cancer (303 with papillary carcinoma and 82 with follicular carcinoma). Measurements: Death, disease progression, and disease-free survival. Results: Total or near-total thyroidectomy was done in 85.3% of patients with papillary carcinoma and 71.3% of patients with follicular cancer. Overall surgical complication rate was 14.3%. Total or near-total thyroidectomy improved overall survival (risk ratio [RR], 0.37 [95% CI, 0.18 to 0.75]) but not cancer-specific mortality, progression, or disease-free survival in patients with papillary cancer. No effect of extent of surgery was seen in patients with follicular thyroid cancer. Postoperative iodine- 131 was given to 85.4% of patients with papillary cancer and 79.3% of patients with follicular cancer. In patients with papillary cancer, radioiodine therapy was associated with improvement in cancer-specific mortality (RR, 0.30 [CI, 0.09 to 0.93 by multivariate analysis only]) and progression (RR, 0.30 [CI, 0.13 to 0.72]). When tall-cell variants were excluded, the effect on outcome was not significant. After radioiodine therapy, patients with follicular thyroid cancer had improvement in overall mortality (RR, 0.17 [CI, 0.06 to 0.47]), cancer-specific mortality (RR, 0.12 [CI, 0.04 to 0.42]), progression (RR, 0.21 [CI, 0.08 to 0.56]), and disease- free survival (RR, 0.29 [CI, 0.08 to 1.01]). External radiation therapy to the neck was given to 18.5% of patients and was not associated with improved survival, lack of progression, or disease-free survival. Conclusions: This study supports improvement in overall and cancer-specific mortality among patients with papillary and follicular thyroid cancer after postoperative iodine-131 therapy. Radioiodine therapy was also associated with improvement in progression in patients with papillary cancer and improvement in progression and disease-free survival in patients with follicular carcinoma.

Original languageEnglish (US)
Pages (from-to)622-627
Number of pages6
JournalAnnals of internal medicine
Volume129
Issue number8
DOIs
StatePublished - Oct 15 1998

ASJC Scopus subject areas

  • Internal Medicine

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    Taylor, T., Specker, B., Robbins, J., Sperling, M., Ho, M., Ain, K., Bigos, S. T., Brierley, J., Cooper, D., Haugen, B., Hay, I., Hertzberg, V., Klein, I., Klein, H., Ladenson, P., Nishiyama, R., Ross, D., Sherman, S., & Maxon, H. R. (1998). Outcome after treatment of high-risk papillary and non-Hurthle-cell follicular thyroid carcinoma. Annals of internal medicine, 129(8), 622-627. https://doi.org/10.7326/0003-4819-129-8-199810150-00007