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There were several reports concerning medullary carcinoma. Colombo-Benkmann,
Heidelberg, Germany, reported results of methoxy-iso-butyl-isonitril (MIBI)
99mTC-scanning to localize recurrent medullary thyroid carcinoma (MTC)
in 11 patients with no or suspected recurrences. One patient was correctly
diagnosed as being free of recurrence, whereas in the remaining 10 patients
14 areas were correctly localized by this technique, as confirmed histologically.
(Comment: We like to see results in more patients using this promising
radio-pharmacon.)
Heshmati et al., Paris, France, studied expression of calcitonin
gene-related peptide (CGRP) and of calcitonin (CT) after stimulation with
pentagastrin in 13 patients with MTC and in 16 normals. All patients reacted
dramatically with regard to CT with a mean increment after stimulation
of 1631 % over basal values. Only 3MTC patients had an increment higher
than 100% over basal values regarding CGRP expression. Hardly any stimulation
of expression of both substances was seen in controls. It is concluded
that in most patients with MTC there is a dissociation between CGRP and
CT secretion, although both peptides are encoded by the calcitonin gene
in the thyroid and in the nervous system.
Robinson, Sidney, Australia, studied mutations in the RET oncogen
known to occur in families with MTC and multiple endocrine neoplasia type
2A (MEN 2A). Seven separate mutations have been found in 15 Australian
families. They performed a thyroidectomy in a patient on the basis of a
suspected gene mutation, although in this subject the CT peak after pentagastrin
was just below the upper normal limit (189 pg/ml) being 182pg/ml. This
patient had histologically confirmed c-cell hyperplasia as well as parathyroid
hyperplasia. Three at risk individuals in MEN 2A families had calcitonin
peaks at 194 pg/ml, 189 pg/ml and 160 pg/ml, and were shown not to be gene
carriers, and thyroidectomy was not performed. A fourth family member had
a peak of 98 pg/ml, and underwent thyroidectomy. The thyroid gland was
normal and he was subsequently shown not to be a gene carrier. These studies
indicate the utility of direct mutation detection and pentagastrin stimulation
in the management of the MEN 2 syndromes.
Pacini, Pisa, Italy, reported screening for RET gene mutations
in MEN 2 A and B, and in sporadic MTC. They found mutations both in families
with MEN 2A and MEN 2B (only 1 family). Furthermore somatic point mutations
were found in 50 % of sporadic MTC. Finally a RET mutation was also found
in a case of a combination of MEN 2A and cutaneous lichen amyloidosis.
RET mutations in the tumor DNA were found in 9/16 sporadic patients but
in 2patients the mutation was also present in constitutional DNA indicating
that these cases were wrongly classified as sporadic. Also several reports
were presented concerning differentiated thyroid carcinoma.
Kolenda, Toronto, Canada, retrospectively evaluated the utility
of near total thyroidectomy (NTT) in three groups of patients: Gr I (n
= 64) had NTT for solitary nodule; Gr II (n = 17) had completion thyroidectomy
following previous lobectomy and Gr III (n = 14) had NTT for palpable bilateral
disease. In Gr I patients 73.5 % had ca., confined to index lobe only;
18.8 % had bilateral ca., and 7.8 % had benign disease only in index lobe.
In Gr II residual ca. was detected in 5/17 (29 %) after completion thyroidectomy.
In Gr III bilateral ca. was detected in 57 %. It is concluded that NTT
ensures a more complete irradication and enhances effectiveness of radioiodine
ablation as well as subsequent utility serum TG measurement as a marker
for recurrence. The authors also found that contralateral recurrences are
often not detectable by palpation, 131I scanning, or ultrasound.
Baqai, Los Angeles, CA, USA, reported 18FDG-PETscanning in 11
patients with differentiated thyroid carcinoma, who had negative (2 - 5
mCi) 131I diagnostic scans and persistently detectable TG serum values,
while being on T4 suppression. Patients were initially treated with total
thyroidectomy and 131I ablation. All patients showed abnormal 18FDG-uptake
in one or more sites. It is concluded that this technique of scanning provides
a sensitive tool for diagnosing differentiated thyroid carcinoma localization,
especially in patients with detectable serum TG and negative diagnostic
131I scans. This technique avoids the need for withdrawal of T4. A disadvantage
is, that the technique is very expensive. (Comment: This is a very interesting
and potential important report and confirms the potential use of FDG as
a non-specific radiopharmacon for the detection of cancer sites. It is
not known if in this study positive scanning results were histologically
verified as tumorsites.)
About another technique, that of 99mTc-sestamibi (Methoxy-iso-Butyl-Isomitrile,
MIBI) scanning in differentiated thyroid carcinoma was reported by Elser,
Heidelberg, Germany. Results were compared with 131I scintigraphy (ISc)
and 46 patients with suspected or proven recurrence after total thyroidectomy
and ablative radioiodine therapy were investigated. Local recurrences were
detected in 94 % in MIBI and 63 % in ISc. Pulmonary localizations and skeletal
localizations were detected in 77 and 83 % respectively in MIBI and in
39 and 44 % in ISc. The authors stress the importance of MIBI scanning
in patients suspected of having local recurrences in differentiated thyroid
carcinoma.
Basschieri, Pisa, Italy, investigated the prevalence of thyroid
nodules in 59 male medical X-ray workers, and compared the results with
a control group of 130 males without occupational radiation exposure. Ultrasound
scanning revealed in 41 % of exposed subjects thyroid nodules versus 19
% in controls. Fine needle aspiration did not disclose thyroid malignancy
in any case. Thyroid function parameters were normal in all subjects of
both groups. Radiation induced nodule formation was especially higher in
younger subjects.
Kimura et al., Basel, Switzerland and Sao Paulo, Brasil, studied
the expression of transforming growth factor (TGF) b1 and b3, using immunoenzymatic
staining after tissues have been exposed to antibodies against these TGF's.
Ten benign and 10 malignant human thyroids were studied and it was found,
that distribution of both TGF's was homogenous in malignant tumors, but
in benign tumors both TGF's were only expressed in morphologically proliferative
areas. From these results it is concluded that TGF b1 and b3 may contribute
to benign and malignant growth in human thyroids.
Willemshurst, St. Leonards, Australia, reported the outcome of
treatment of differentiated thyroid carcinoma in 658 patients over 26 years.
The treatment protocol was uniform in that a total thyroidectomy, if necessary
with neck dissection, was performed followed by postoperative 131I scan
and, if residual uptake was present, an ablative dose of 150 mCi 131I.
T4 was given in suppresive doses and 131I scans, and serum TG measurements
were repeatedly done, and 150 mCi 131I was administered when uptake of
radionuclide was detected. The papillary carcinoma group consisted of 489
patients and the follicular carcinoma group of 169 patients. Ten years
survival rates were 94 % (pap. ca.) and 88 % (fol. ca.). Survival was not
significantly different between male and female patients, nor between both
carcinoma groups. Age was the most significant predictor of survival. Compared
with age <40 years, risk of dying was increased 29 times for age group
40-70 years, and 270 times for patients over 70years. The presence of metastases
increased risk of dying by a factor 2.1 and larger tumor size was associated
with increased risk of death (p = 0.004).
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