Purpose: We aimed to explore the efficacy of 90 Yttrium^1,4,7,N ¶,N

BACKGROUND: Procalcitonin has been well established as an important marker of sepsis and systemic infection. The authors evaluated the diagnostic and predictive value of calcitonin and its prohormone procalcitonin in medullary thyroid cancer. METHODS: The authors systematically explored the ability of calcitonin and procalcitonin to identify medullary thyroid cancer and predict the endpoints local recurrence and distant metastases, as well as the progression-free survival. Patients with C-cell hyperplasia; patients after thyroidectomy for differentiated thyroid cancer, goiter, or Graves disease; and healthy subjects served as controls. The study was performed in accordance with the Reporting Recommendations for Tumor Marker Prognostic Studies of the National Cancer Institute. RESULTS: Sixtynine medullary thyroid cancer patients and 96 controls were included (median observed interval: 10.9 years [range, 1.4-47.5 years]; 981.8 patient-years). The 1-year, 5-year, 10-year, and 20-year recurrence rates were 9%, 34%, 45%, and 56%, respectively. Calcitonin had a higher diagnostic accuracy for detecting medullary thyroid cancer than procalcitonin ( The results of the current study indicate a superior diagnostic accuracy of calcitonin and an independent predictive value of the procalcitonin:calcitonin ratio. These findings may lead to improved diagnostic and therapeutic strategies for medullary thyroid cancer patients. Cancer 2010;116:31-40.

BACKGROUND:The authors aimed to explore the efficacy of 90Yttrium‐1,4,7,10‐tetra‐azacyclododecane N,N′,N″,N‴‐tetraacetic acid [90Y‐DOTA]‐Tyr3‐octreotide (TOC) in advanced iodine‐refractory thyroid cancer.METHODS:In a phase 2 trial, the authors investigated biochemical response (assessed by serum thyroglobulin levels), survival, and the long‐term safety profile of systemic [90Y‐DOTA]‐TOC treatment in metastasized iodine‐refractory thyroid cancer. Adverse events were assessed according to the National Cancer Institute criteria. Survival analyses were performed by using multiple regression models.RESULTS:A total of 24 patients were enrolled. A median cumulative activity of 13.0 GBq (range, 1.7‐30.3 GBq) was administered. Response was found in 7 (29.2%) patients. Eight (33.3%) patients developed hematologic toxicity grade 1‐3, and 4 (16.7%) patients developed renal toxicity grade 1‐4. The median survival was 33.4 months (range, 3.6‐126.8 months) from time of diagnosis and 16.8 months (range, 1.8‐99.1 months) from time of first [90Y‐DOTA]‐TOC treatment. Response to treatment was associated with longer survival from time of diagnosis (hazard ratio [HR], 0.17; 95% confidence interval [CI], 0.03‐0.92; P = .04) and from time of first [90Y‐DOTA]‐TOC therapy (HR, 0.20; 95% CI, 0.04‐0.94; P = .04). The visual grade of scintigraphic tumor uptake was not associated with treatment response (odds ratio [OR], 0.98; 95% CI, 0.26‐3.14; P = 1.00).CONCLUSIONS:Response to [90Y‐DOTA]‐TOC in metastasized iodine‐refractory thyroid cancer was associated with longer survival. Upcoming trials should aim to increase the number of treatment cycles. Cancer 2009. © 2009 American Cancer Society.

The free extended lateral arm flap (ELAF) has gained increasing popularity thank to its slimness and versatility, longer neurovascular pedicle, and greater flap size when compared with the original flap design. The aim of this study was to assess the donor-site morbidity associated with this extended procedure. A retrospective study of 25 consecutive patients analyzing postoperative complications using a visual analogue scale questionnaire revealed high patients satisfaction and negligible donor-site morbidity of the ELAF. Scar visibility was the commonest negative outcome. Impaired mobility of the elbow had the highest correlation with patient dissatisfaction. Sensory deficits or paresthetic disorders did not affect patient satisfaction. The extension of the lateral arm flap and positioning over the lateral humeral epicondyle is a safe and well-accepted procedure with minimal donor-site morbidity. To optimize outcomes, a maximal flap width of 6 or 7 cm and intensive postoperative mobilization therapy is advisable.