2013
DOI: 10.1111/cen.12001
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Is basal ultrasensitive measurement of calcitonin capable of substituting for the pentagastrin‐stimulation test?

Abstract: The ultrasensitive CT assay reduces the false-negative rate of basal CT measurements when diagnosing familial MTC and in postoperative follow-up compared with previously used assays. However, its sensitivity to detect C-cell disease remains lower than that of the Pg-stimulation test.

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Cited by 20 publications
(14 citation statements)
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“…If we could divide these negative calcitonin MTC into two categories, one were cancer cells show diffuse staining for calcitonin and another with weak and focal immunoreactivity, we could say that in the first category MTC maintain its ability to produce calcitonin but lose its ability to secrete it, whereas in the second category cancer cells cannot produce calcitonin. In regards to the first type of negative calcitonin MTC, one could hypothesize that there might be a defect in the secretory mechanism, or that the tumor preferential secrete precursor peptides and aberrant forms of calcitonin instead of the mature molecule [6], or that a mutation in the calcitonin/CGRP gene is responsible for the normal or reduced serum calcitonin [4]. When it comes to the second category, we already know that in progressive disease calcitonin levels may decrease due to dedifferentiation [9,15], we could consider that tumor cells with weak calcitonin expression indicate a loss of function and there for dedifferentiation and more aggressive nature [7,14].…”
Section: Discussionmentioning
confidence: 99%
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“…If we could divide these negative calcitonin MTC into two categories, one were cancer cells show diffuse staining for calcitonin and another with weak and focal immunoreactivity, we could say that in the first category MTC maintain its ability to produce calcitonin but lose its ability to secrete it, whereas in the second category cancer cells cannot produce calcitonin. In regards to the first type of negative calcitonin MTC, one could hypothesize that there might be a defect in the secretory mechanism, or that the tumor preferential secrete precursor peptides and aberrant forms of calcitonin instead of the mature molecule [6], or that a mutation in the calcitonin/CGRP gene is responsible for the normal or reduced serum calcitonin [4]. When it comes to the second category, we already know that in progressive disease calcitonin levels may decrease due to dedifferentiation [9,15], we could consider that tumor cells with weak calcitonin expression indicate a loss of function and there for dedifferentiation and more aggressive nature [7,14].…”
Section: Discussionmentioning
confidence: 99%
“…Although MTC is considered a well differentiated tumour, it is quite aggressive [3]. In fact it is the second most aggressive thyroid cancer after anaplastic carcinoma [4], with a mortality rate that ranges between 13, 4 -38% [2][3][4][5]. Its poor prognosis relies not only on its aggressive nature but also on its limited response to chemotherapy and radiation [6].…”
Section: Introductionmentioning
confidence: 99%
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