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Anaplastic carcinoma of the thyroid: A 24‐year experience
239
Citations
15
References
1995
Year
Surgical OncologyMedicineCancer ManagementSurgical PathologyThyroid DiseaseCancer DiagnosisThyroid DisordersSurgeryHead And Neck CancerComplete ResectionNeck OncologyOncologyRadiation OncologyThyroid CancerCancer ResearchAnaplastic Carcinoma
Abstract Background. Anaplastic carcinoma of the thyroid gland is a lethal entity; few patients live more than 12 months following diagnosis. We retrospectively reviewed the experience with this entity at our cancer institute and identified a subgroup of patients with complete resection who have a 60% 5‐year survival. Methods. Twenty‐one cases of anaplastic carcinoma of the thyroid gland were analyzed retorspectively with respect to prognostic factors influencing survival. This represents 2.7% of 771 cases of thyroid cancer seen at our institution from 1968 to 1992. The median age at presentation was 65.1 years; male/female ratio was 1:1.1; and the most common symptom was a rapidly enlarging neck mass (76%). Results. Estimated 5‐year survival was 10% (median: 4.5 months). Tumor size less than 6.0 cm ( p = .004) and female gender ( p = .02) were significant prognostic factors. Five patients who underwent complete resection had an estimated 5‐year survival of 60% (median: 131 months). Four of these patients had postoperative radiotherapy with or without sequential chemotherapy. Two of these patients survived more than 10 years, and a third remains alive without disease at 26 months. Conclusions. Complete resection and multimodality therapy result in long‐term survival for a subgroup of patients with anaplastic thyroid carcinoma. © 1995 Jons Wiley & Sons, Inc.
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