|Year : 2015 | Volume
| Issue : 2 | Page : 101-108
Utility of 99m Tc-Hynic-TOC in 131I Whole-Body Scan Negative Thyroid Cancer Patients with Elevated Serum Thyroglobulin Levels
Ajit S Shinto1, KK Kamaleshwaran1, Madhav Mallia2, Aruna Korde2, Grace Samuel2, Sharmila Banerjee2, Pavanasam Velayutham1, Suresh Damodharan1, Madhu Sairam1
1 Department of Nuclear Medicine, KMCH, Coimbatore, Tamil Nadu, India
2 Isotope Application and Radiopharmaceuticals Division, BARC, Mumbai, Maharashtra, India
|Date of Web Publication||15-May-2015|
Ajit S Shinto
Department of Nuclear Medicine, KMCH, Coimbatore, Tamil Nadu 641 014
| Abstract|| |
Several studies have reported on the expression of somatostatin receptors (SSTRs) in patients with differentiated thyroid cancer (DTC). The aim of this study was to evaluate the imaging abilities of a recently developed Technetium-99m labeled somatostatin analog, 99m Tc-Hynic-TOC, in terms of precise localization of the disease. The study population consisted of 28 patients (16 men, 12 women; age range: 39-72 years) with histologically confirmed DTC, who presented with recurrent or persistent disease as indicated by elevated serum thyroglobulin (Tg) levels after initial treatment (serum Tg > 10 ng/ml off T4 suppression for 4-6 weeks). All patients were negative on the Iodine-131 posttherapy whole-body scans. Fluorine-18 fluorodeoxyglucose positron emission tomography ( 18 F-FDG PET) was performed in all patients. SSTR scintigraphy was true positive in 23 cases (82.1%), true negative in two cases (7.1%) and false negative in three cases (10.7%) which resulted in a sensitivity of 88.46%, specificity of 100% and an accuracy of 89.2%. Sensitivity of 99m Tc-Hynic-TOC scan was higher (93.7%) for patients with advanced stages, that is stages III and IV. 18 F-FDG showed a sensitivity of 93.7%, a specificity of 50% and an accuracy of 89.3%. 18 F-FDG PET was found to be more sensitive, with lower specificity due to false positive results in 2 patients. Analysis on a lesion basis demonstrated substantial agreement between the two imaging techniques with a Cohen's kappa of 0.66. Scintigraphy with 99m Tc-Hynic-TOC might be a promising tool for treatment planning; it is easy to perform and showed sufficient accuracy for localization diagnostics in thyroid cancer patients with recurrent or metastatic disease.
Keywords: Fluorodeoxyglucose positron emission tomography, Hynic-TOC, single-photon emission computed tomography, thyroglobulin elevated, thyroid cancer, whole-body scan negative
|How to cite this article:|
Shinto AS, Kamaleshwaran K K, Mallia M, Korde A, Samuel G, Banerjee S, Velayutham P, Damodharan S, Sairam M. Utility of 99m Tc-Hynic-TOC in 131I Whole-Body Scan Negative Thyroid Cancer Patients with Elevated Serum Thyroglobulin Levels. World J Nucl Med 2015;14:101-8
|How to cite this URL:|
Shinto AS, Kamaleshwaran K K, Mallia M, Korde A, Samuel G, Banerjee S, Velayutham P, Damodharan S, Sairam M. Utility of 99m Tc-Hynic-TOC in 131I Whole-Body Scan Negative Thyroid Cancer Patients with Elevated Serum Thyroglobulin Levels. World J Nucl Med [serial online] 2015 [cited 2020 Aug 11];14:101-8. Available from: http://www.wjnm.org/text.asp?2015/14/2/101/154229
| Introduction|| |
Most of the differentiated thyroid cancer (DTC) variants have a good prognosis, with a fair chance of complete cure, good overall survival and lower chances of locoregional and distant metastases, if treated adequately.  Routine postradioiodine ablation surveillance and follow-up in clinical setting is by serial serum thyroglobulin (Tg) measurement, which is highly sensitive as well as specific for DTC disease burden. ,, This situation is, however, complicated when a raised Tg level is accompanied by a negative 131 I/ 123 I whole-body scan (WBS). The potential explanation being the loss of ability of the underlying malignant cells to concentrate iodine. These patients belong to a cohort who may not benefit from radioiodine therapy. Thus, other imaging modalities like Fluorine-18 fluorodeoxyglucose positron emission tomography ( 18 F-FDG PET) or different radiotracers like 99m Tc-Sestamibi or 99m Tc-Tetrofosmin or 201 Tl need to be used for disease localization. Treatment options would also vary depending on the site and extent of recurrent/metastatic disease. ,,,
Despite being nonspecific tumor markers, with possible mitochondrial localization, single-photon emission computed tomography (SPECT) radiopharmaceuticals such as 201 Tl, 99m Tc-Sestamibi or 99m Tc-Tetrofosmin have reasonable accuracy. ,, However, they have been replaced by 18 F-FDG, which localizes in recurrent or metastatic tumors due to increased glucose demand and has proven to be very sensitive method in the follow-up algorithm of thyroid cancer patients. But above mentioned SPECT - radiopharmaceuticals are more economical than 18 F-FDG, are easily available, can be performed on suppressive thyroxine therapy, are easy to prepare and impart lower radiation dose to the patient than 18 F-FDG. Utility of 18 F-FDG PET, however has been proven even in clinical scenarios where conventional imaging (ultrasound, computed tomography [CT], magnetic resonance imaging [MRI]) is normal. ,,,,,,,
Utility of somatostatin receptor (SSTR) scintigraphy, which has become the gold standard for the diagnosis, staging and treatment response assessment in almost all neuroendocrine tumors, ,,,, has also been explored for various nonneuroendocrine tumors. Most of the studies reported earlier were using 111 In-diethylenetriaminepentaacetic acid (DTPA)-octreotide (octreoscan), ,,,,,,,, and could not clearly define the utility of this technique. In retrospect, it could be due to the inherent drawbacks of 111 In-isotope for imaging applications and small, nonhomogenous patient population with diverse histopathologiocal variants of DTC. 
In the present study, we have evaluated 99m Tc-Hynic-TOC, prepared using an indigenously developed lyophilized kit, , in a clinical setting of noniodine concentrating DTC's with raised Tg levels. The advantages with this radiopharmaceutical include the use of 99m Tc-isotope, which is having favorable nuclear characteristics for imaging applications when compared to 111 In, easy availability from 99 Mo/ 99m Tc generator, ease of preparation, faster pharmacokinetics, improved background clearance, better image resolution, and lower cost. 
The purpose of this study was to evaluate the efficacy of 99m Tc-Hynic-TOC for the detection of SSTR-positive lesions in patients who have had thyroidectomy, followed by radioiodine ablation and now presenting with raised Tg levels and negative follow-up whole-body radioiodine scans. In all patients, a correlative whole-body 18 F-FDG PET was also obtained to assess the tumor biology, aggressiveness and the feasibility of chemotherapy or peptide receptor radionuclide therapy (PRRT).
| Materials and Methods|| |
Patient eligibility criteria: A total of 28 patients (16 men, 12 women; age range: 39-72 years; mean age ± SD, 64.8 ± 7.6 years) with histologically confirmed DTC were included for this study.
The patients had undergone near-total thyroidectomy and immediate radioactive ablation between 4 and 12 weeks after surgery and presented with either recurrent or persistent disease as indicated by elevated Tg levels on routine follow-up (half-yearly) with negative 131 I WBS. None of the patients was treated with empiric oral 131 I following a negative low dose scan. Correlative 99m Tc-Hynic-TOC scans were performed within 1-week of the 131 I WBS without restarting the patients on Thyroxine suppression. Raised Tg levels were confirmed on two separate occasions with or without thyroxine suppression.
Out of the 28 patients, 14 suffered from follicular carcinoma, 10 from papillary carcinoma and four from Hurthle cell carcinoma. The tumor node metastasis classification according to Union for Internationale Cancer Control,  edition 1997, was used to classify the primary tumor.
Initial pathologic tumor stages were as follows. T2 in 5 patients, T3 in 16 patients and T4 in 7 patients. Five patients were node negative (N0), 14 patients were node positive (N1a = 6, and N1b = 8) and 9 patients had no information concerning lymph node metastasis (Nx). Among the 28 patients, six initially had distant metastases (M1). The clinical staging represented the highest stage achieved during the patient's course and was determined according to the American Joint Committee on Cancer classification.  Stage I was present in 3 patients, stage II in 5 patients, stage III in 12 patients and stage IV in 8 patients. The frequency of metastatic disease was quite high in the patient group and Tg levels on T4 of far over 100 in 11 cases suggest a very advanced population that may be quite different from other groups described in the literature. Patient characteristics are summarized in [Table 1]. The study was approved by the local ethical committee and was performed in accordance with the declaration of Helsinki. All patients gave their written informed consent to participation.
|Table 1: Patient characteristics and results in the patients without detectable pathology prior to 99mTc-Hynic TOC |
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Pretreatment evaluation and posttherapy scanning
Because of increasing serum Tg levels during thyroid stimulating hormone (TSH) suppression, patients were referred to our department for administration of high-dose radioiodine therapy under TSH stimulation. All patients had the scan after 4-6 weeks of L-thyroxine withdrawal. X-ray of the chest and ultrasound of the neck were regularly performed in all patients. CT of the chest (without contrast medium) was also obtained in all patients. Five patients had received a single sitting of high-dose Iodine-131 therapy, six patients had two sittings, 12 patients had three sittings, and five patients had four sittings of Iodine-131 therapy. WBSs were obtained with a double-headed camera (Siemens Symbia-T with high-energy collimator), 1 or 2 days after the oral administration of 131 I (1.5-3 mCi). WBS results were negative in all patients.
Lyophilized Hynic-TOC kit vials were obtained as a gift from Radiopharmaceuticals Division, Bhabha Atomic Research Centre, Mumbai. Detailed procedure for the preparation lyophilized Hynic-TOC kit will be reported elsewhere.  Each lyophilized kit vial contains Hynic-TOC (30 ug), EDDA (10 mg), tricine (20 mg), sodium phosphate dibasic heptahydrate (4.5 mg), sodium phosphate monobasic (1 mg) and stannous chloride dehydrate (40 ug). The lyophilized kits were subjected to thorough quality control checks, including bacterial endotoxin test and sterility test, at the manufacturer's end before releasing for clinical use.
The radiolabeling procedure was performed under aseptic conditions. 99m Tc-Hynic-TOC was prepared by adding 10-60 mCi (370-2220 MBq) of freshly eluted sterile 99m Tc-sodium pertechnetate in 1-3 ml of sterile saline, obtained from 99 Mo/ 99m Tc alumina column generator (Radioisotope Center POLATOM), into the kit vial and heating the vial in boiling water bath for 20 min.
The radiochemical purity of 99m Tc-Hynic-TOC determined by standard quality control procedure was between 92% and 98%, with the free pertechnetate content in the range of 2.93-1.54%.
About 740 MBq - 925 MBq (20-25 mCi) of 99m Tc-Hynic-TOC was administered in each patient which corresponded to ~10 ug of Hynic-TOC. First image was acquired ~1.5 h postinjection. In select cases, when there was difficulty in the evaluation of the abdominal region due to the elimination of the radiopharmaceutical via the gastrointestinal tract, a second image was acquired after waiting for another 2 h. A WBS as well as SPECT of the region where the tumor was located (e.g. head, neck, thorax, abdomen, pelvis) was also acquired. No contrast agent was used. The whole-body images were acquired at a table speed of 8 cm/min in a dual-headed gamma camera (Siemens Symbia T equipped with an LEHR collimator, with energy peak of 140 KeV ± 15% window level).
In the SPECT/CT system, the CT acquisition was performed with a slice thickness of 4 mm and a pitch of one on a helical dual-slice CT unit. Images were acquired using a matrix of 512 × 512 pixels and a pixel size of 1 mm. SPECT data were acquired using a matrix of 128 × 128 pixels and a slice thickness of 1.5 mm. CT-based attenuation correction of the emission images was used. SPECT images were reconstructed by iterative method ordered subset expectation maximization (OSEM) (two iterations and eight subsets).
Fluorine-18 fluorodeoxyglucose positron emission tomography
All patients received 370 MBq (10 mCi) 18 F-FDG after a fasting period of 5-12 h while they are off thyroxine therapy. Trans axial imaging was performed using a PET-CT scanner (Siemens Biograph 6, Germany) at 45 and 90 min after intravenous injection of the tracer. The emission scan was acquired from the head to upper legs with five to six bed positions (4 min/bed position). Iterative image reconstruction was performed with an OSEM algorithm (two iterations, 28 subsets). Abdominal, chest and head CT-scanning was performed with 3-mm contiguous sections using a 512 × 512 matrix, without infusion of contrast medium.
Image and data analysis
The images obtained were interpreted by two nuclear medicine physicians (AS., KK.) blinded to the results of conventional or PET/CT examinations. Any focal tracer accumulation exceeding normal regional tracer uptake was rated as a pathological finding (tumor uptake). In relevant areas, SPECT images were available to the physicians. All data were analyzed on a SIEMENS SYMBIA system. In both groups, readers of the scans were blinded to the underlying pathology and to the results of the standard staging procedures, including PET data. All images were visually evaluated and abnormal scintigraphic findings were classified according to the sites typical for recurrences or metastases (local recurrence, lymph node of the neck, mediastinum, lungs and bone structures) and other sites. The reference standard against which the results of the 99m Tc-Hynic-TOC procedure were measured was based on the results of all of the imaging procedures which include serial follow-up, morphological imaging and histopathology of surgical specimens or biopsy (12 patients). All patients underwent ultrasound of the neck and imaging with CT and MRI (n = 2). 18 F-FDG PET was performed in all patients. The time interval between 99m Tc-Hynic-TOC scintigraphy and 18 F-FDG PET did not exceed 2 weeks and both techniques were prospectively compared. The viewers of the studies were blinded to findings of other methods.
Blood samples for measuring serum Tg were taken during suppression therapy as well as prior to scintigraphy off - Thyroxine therapy. The Tg levels were determined in duplicate by a sensitive, commercially available radio-immunoassay.
99m Tc-Hynic-TOC images were classified as true positive (TP), true negative (TN), false positive (FP) or false negative (FN) comparing with the gold standard (histopathology or other imaging techniques), as described above. The Chi-square test for independence, or the Fisher exact test when appropriate, was used to evaluate differences in lesion-detectability with 99m Tc-Hynic-TOC when subgroups of the patients being investigated were statistically compared. All P < 0.05 were considered to be statistically significant. The McNemar test of correlated properties was used to assess the statistical significance of the difference between the scintigraphic results of 99m Tc-Hynic-TOC and 18 F-FDG PET. Analysis was performed both on a lesion and a patient basis. Two-sided P < 0.05 were considered as significant. Statistical analysis was carried out with SPSS software (Statistical Package for Social Sciences).
| Results|| |
[Table 1] summarizes the clinical information of each patient. Among the 28 cases, SSTR scintigraphy was TP in 23 (82.1%), TN in 2 (7.1%) and FN in 3 (10.7%) cases. No FP results were observed. Overall, the sensitivity of 99m Tc-Hynic-TOC for identification of thyroid cancer was 88.46% (95% CI 69.82-97.42) on a patient basis, with a specificity of 100% and an accuracy of 89.2%. Sensitivity of 99m Tc-Hynic-TOC scan was higher (93.75%) for (n = 17) with advanced stages, that is stages III and IV, than for stage I and II (n = 11) disease, in which sensitivity was 80%. These findings are summarized in [Table 2].
Site-related findings are listed in [Table 3]. When 99m Tc-Hynic-TOC was correlated with other imaging modalities or histopathology for analysis on a lesion basis, 101 tumor foci were localized in 23 patients, affecting the following five tissues: Local recurrence (n = 6 patients), lymph node metastases in the neck (n = 14), mediastinum (n = 12), pulmonary metastases (n = 48) and bone (n = 21). In addition to pulmonary metastasis and local tumor recurrence as assessed by biopsy, 99m Tc-Hynic-TOC identified a solitary brain metastasis in one patient. These findings are summarized in [Table 4].
99m Tc-Hynic-TOC and thyroglobulin evaluation
Patients were categorized into two groups in order to evaluate the influence of the current Tg level on lesion-detectability with 99m Tc-Hynic-TOC. First group had initial serum Tg levels of <30 ng/ml (n = 12) and with the second group had the initial serum Tg levels of >30 ng/ml (n = 16). In the group with elevated Tg levels (>30 ng/ml) (n = 16), the scan result was true positive in 15 cases and FN in 1. In the 12 patients with Tg levels lower than 30 ng/ml, scanning was negative in four patients, which include three TN and 1 FNs. Eight cases were true positive.
The fraction of true positive 99m Tc-Hynic-TOC uptake in lesions was positively correlated with elevated Tg levels (>30 ng/ml), showing a significant difference (P < 0.01). The lowest Tg level with unequivocal positive 99m Tc-Hynic-TOC findings was 6.7 ng/ml (in whom lymph node involvement was revealed), and the highest Tg level with FN 99m Tc-Hynic-TOC scintigraphy was 137 ng/ml. This patient presented with multiple pulmonary metastases, all of which were smaller than 1 cm.
Comparison of results between 99m Tc-Hynic-TOC and 18 F-FDG PET are given in [Table 3]. In five cases (17.8%), 99m Tc-Hynic-TOC scintigraphy was negative, while 18 F-FDG PET was negative in three cases (10.7%). In two of the five patients with negative 99m Tc-Hynic-TOC scans, further clinical examinations did not reveal any pathological findings and serum Tg levels remained stable for at least 1-year. These cases were considered TN. 26 of the 28 patients (92.8%) were proven to have disease, which confirms the advanced nature of our patient group. False negative 99m Tc-Hynic-TOC scan were obtained in three cases (10.7%) while a single FN scan (3.5%) was observed with 18 F-FDG PET in a patient with lung and cerebral metastases. Per patient analysis comparing the scan results of 99m Tc-Hynic-TOC and 18 F-FDG showed no significant difference between PET and 99m Tc-Hynic-TOC imaging (P = 0.6) using the McNemar test. Illustrative examples of HYNIC TOC and FDG PET CT scans in patients presenting with thyroid bed recurrence, cervical node, lung , mediastinal and skeletal metastases are shown in [Figure 1], [Figure 2], [Figure 3], [Figure 4].
|Figure 1: Whole-body Hynic-TOC anterior image (a) showing moderate uptake in the recurrence in the thyroid bed and cervical nodes, whole-body fluorodeoxyglucose-positron emission tomography/computed tomography (CT) maximum intensity projection image (b) intense uptake in the right neck nodes. Fused Hynic-TOC single-photon emission computed tomography/CT (c) uptake in the right level II cervical nodes and thyroid bed|
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|Figure 2: Whole-body Hynic-TOC anterior image (a) showing moderate uptake in the right cervical node, whole-body fluorodeoxyglucose-positron emission tomography/computed tomography (CT) maximum intensity projection image (b) intense uptake in the right neck nodes and Fused Hynic-TOC single-photon emission computed tomography/CT(c) uptake in the right level II cervical nodes|
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|Figure 3: Whole-body Hynic-TOC anterior image (a) showing mild uptake in the right pleural thickening, whole-body fluorodeoxyglucose-positron emission tomography/computed tomography (CT) maximum intensity projection image (b) intense uptake in the right pleural thickening and Fused Hynic-TOC single-photon emission computed tomography/CT (c) uptake in the right pleural thickening|
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|Figure 4: Whole-body Hynic-TOC anterior image (a) showing uptake in the right humerus and mediastinal nodes. Whole-body FDG PET/CT maximum intensity projection image (b) intense uptake in the right humerus, lung nodules, mediastinal, abdominal and aortocaval lymph nodes and fused Hynic-TOC single-photon emission computed tomography/CT (c) uptake in the shaft of right humerus and mediastinal nodes|
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In addition, a site-specific evaluation was performed. Tissue-related abnormal uptake is reported in [Table 2]. Analysis on a lesion-by-lesion basis also emphasized substantial agreement between the imaging techniques.
Twelve patients were referred for receptor-mediated radionuclide therapy using 177 Lu-DOTA TATE or 90 Y-DOTA TATE, or a cocktail therapy with both, based on the uptake observed with 99m Tc-Hynic-TOC radiopharmaceutical found in tumor lesions. All patients had extended disease with more than one affected tissue site. Each of them responded under this therapy regimen and stable disease was achieved for at least 6 months in all patients. Each patient was well informed about this new treatment option, and the therapy was well-tolerated.
| Discussion|| |
In DTC patients, imaging with 111 In-DTPA-Octreotide has demonstrated high uptake in some cases, but the reported sensitivities vary significantly among different studies.  This study was specifically designed to evaluate the clinical potential of 99m Tc-Hynic-TOC for tumor localization in WBS negative DTC patients with elevated Tg levels under TSH stimulation. 
Our results demonstrate reasonably accurate and favorable imaging ability of this new tracer in DTC patients with an overall sensitivity comparable and specificity higher than 18 F-FDG PET. The results obtained indicate that, with time, lesions that lose their ability to concentrate iodine have a higher glucose uptake rate, at the same time a significant percentage of such lesions still retain their ability to express SSTR. In comparison to similar studies, the overall sensitivity of 99m Tc-Hynic-TOC in our study is better than previously reported with 111 In-DTPA-Octreotide as well as with the same agent (19, 20, 23, 25-27). This favorable result could be due to the fact that imaging was carried out at the time of TSH stimulation. It was also shown that there was a higher probability for a positive scan result in patients with higher Tg levels exceeding 30 ng/ml, which might be mainly attributed to the tumor load.
Another interesting finding is that 18 F-FDG PET outperformed 99m Tc-Hynic-TOC tracer in detecting lesions, especially smaller than 1 cm in size, and more so in the case of pulmonary metastases. These patients had a very high Tg level and tumor load, but no SSTR uptake, which could be due to a higher state of de-differentiation resulting in high-grade 18 F-FDG uptake. Another possible explanation is the higher spatial resolution of PET. Thus, 99m Tc-Hynic-TOC and 18 F-FDG PET have completely different mechanisms of localization and could be considered complimentary in assessing the tumor biology and aggressiveness. This potentially explains the findings in patients in whom 18 F-FDG PET picked up lesions not demonstrated on 99m Tc-Hynic-TOC. 
In the present study, though the statistical diagnostic efficacy was higher for 18 F-FDG PET than for 99m Tc-Hynic-TOC, there were two FP findings with the former, which were negative on 99m Tc-Hynic-TOC. Findings were comparable with a substantial overlap in the lesions detected by each modality, which implies a high degree of agreement between the metabolic pattern and the SSTR status in noniodine-avid lesions.
From a practical and clinical point of view, both techniques can easily be performed without withdrawal of L-thyroxine. Although there is no evidence that serum TSH levels influence the rate of SSTR expression, higher glucose consumption in tumor foci can be observed under TSH stimulation, which could improve the accuracy of 18 F-FDG PET. , As a corollary, a higher sensitivity of 99m Tc-Hynic-TOC scans reported in our series could also be due to increased SSTR expression under TSH stimulation, though it has not been verified or reported. It is important to note that 99m Tc-Hynic-TOC scans will not replace 18 F-FDG PET as the primary imaging modality in this clinical scenario due to less signal to background ratios, less resolution, as well as lack of widespread radio-pharmaceutical availability. Thus 99m Tc-Hynic-TOC shall remain a significant option only in countries with no easy access to PET CT scanners or when 18 F-FDG PET scanning is negative. SSTR imaging could have a higher clinical impact with the added ability to plan for PRRT or cold somatostatin therapy.
Use of a long-acting Octreotide analogue in patients with metastatic thyroid cancer that exhibited SSTR s have been tried and seem promising. , High expression of SSTRs in thyroid carcinoma lesions also offers another treatment option using PRRT, e.g. 177 Lu or 90 Y based SSTR analogues.  We have treated 12 patients with advanced tumor stage who had a very high tumor load. These patients showed good SSTR expression in the lesions on 99m Tc-Hynic-TOC.Thus, 99m Tc-Hynic-TOC can aid in identifying patient suitable for both types of therapy in different clinical scenarios.
| Conclusion|| |
Somatostatin receptor imaging using 99m Tc-Hynic-TOC demonstrates promise as a cost effective, easy to perform and widely available imaging tool in DTC patients with elevated Tg levels and negative WBS. With ongoing research into the utility of somatostatin analogs and PRRT in palliative therapy, SSTR imaging is likely to play a significant role in clinical decision making. The impact of 99m Tc-Hynic-TOC would be higher in developing countries with many centers having no PET/CT facility and when budgetary constraints dictate the type of imaging algorithm followed.
| References|| |
Pacini F, DeGroot LJ. Thyroid neoplasia. In: DeGroot LJ, Jameson JL, editors. Endocrinology. 4 th
ed. Philadelphia: Saunders; 2001. p. 1541-66.
Ronga G, Fiorentino A, Paserio E, Signore A, Todino V, Tummarello MA, et al.
Can iodine-131 whole-body scan be replaced by thyroglobulin measurement in the post-surgical follow-up of differentiated thyroid carcinoma? J Nucl Med 1990;31:1766-71.
Ozata M, Suzuki S, Miyamoto T, Liu RT, Fierro-Renoy F, DeGroot LJ. Serum thyroglobulin in the follow-up of patients with treated differentiated thyroid cancer. J Clin Endocrinol Metab 1994;79:98-105.
Lubin E, Mechlis-Frish S, Zatz S, Shimoni A, Segal K, Avraham A, et al.
Serum thyroglobulin and iodine-131 whole-body scan in the diagnosis and assessment of treatment for metastatic differentiated thyroid carcinoma. J Nucl Med 1994;35:257-62.
Schlumberger MJ. Diagnostic follow-up of well-differentiated thyroid carcinoma: Historical perspective and current status. J Endocrinol Invest 1999;22:3-7.
Feine U, Lietzenmayer R, Hanke JP, Held J, Wöhrle H, Müller-Schauenburg W. Fluorine-18-FDG and iodine-131-iodide uptake in thyroid cancer. J Nucl Med 1996;37:1468-72.
Schlüter B, Bohuslavizki KH, Beyer W, Plotkin M, Buchert R, Clausen M. Impact of FDG PET on patients with differentiated thyroid cancer who present with elevated thyroglobulin and negative 131I scan. J Nucl Med 2001;42:71-6.
Helal BO, Merlet P, Toubert ME, Franc B, Schvartz C, Gauthier-Koelesnikov H, et al.
Clinical impact of (18) F-FDG PET in thyroid carcinoma patients with elevated thyroglobulin levels and negative (131) I scanning results after therapy. J Nucl Med 2001;42:1464-9.
Briele B, Hotze A, Kropp J, Bockisch A, Overbeck B, Grünwald F, et al.
A comparison of 201Tl and 99m
Tc-MIBI in the follow-up of differentiated thyroid carcinomas. Nuklearmedizin 1991;30:115-24.
Lind P, Gallowitsch HJ, Langsteger W, Kresnik E, Mikosch P, Gomez I. Technetium-99m-tetrofosmin whole-body scintigraphy in the follow-up of differentiated thyroid carcinoma. J Nucl Med 1997;38:348-52.
Miyamoto S, Kasagi K, Misaki T, Alam MS, Konishi J. Evaluation of technetium-99m-MIBI scintigraphy in metastatic differentiated thyroid carcinoma. J Nucl Med 1997;38:352-6.
Rubello D, Mazzarotte R, Casara D. The role of technetium-99m methoxyisobutylisonitrile scintigraphy in the planning of therapy and follow-up of patients with differentiated thyroid carcinoma after surgery. Eur J Nucl Med 2000;27:431-40.
Ng DC, Sundram FX, Sin AE 99mTc-sestamibi and 131I whole-body scintigraphy and initial serum thyroglobulin in the management of differentiated thyroid carcinoma. J Nucl Med 2000;41:631-5.
Krenning EP, Kwekkeboom DJ, Bakker WH, Breeman WA, Kooij PP, Oei HY, et al.
Somatostatin receptor scintigraphy with [111In-DTPA-D-Phe1]- and [123I-Tyr3]-octreotide: The Rotterdam experience with more than 1000 patients. Eur J Nucl Med 1993;20:716-31.
Krenning EP, Kwekkeboom DJ, de Jong M, Visser TJ, Reubi JC, Bakker WH, et al.
Essentials of peptide receptor scintigraphy with emphasis on the somatostatin analog octreotide. Semin Oncol 1994;21:6-14.
Lamberts SW, Reubi JC, Krenning EP. Somatostatin and the concept of peptide receptor scintigraphy in oncology. Semin Oncol 1994;21:1-5.
Kwekkeboom D, Krenning EP, de Jong M. Peptide receptor imaging and therapy. J Nucl Med 2000;41:1704-13.
Balon HR, Goldsmith SJ, Siegel BA, Silberstein EB, Krenning EP, Lang O, et al.
Procedure guideline for somatostatin receptor scintigraphy with (111) In-pentetreotide. J Nucl Med 2001;42:1134-8.
Tenenbaum F, Lumbroso J, Schlumberger M, Caillou B, Fragu P, Parmentier C. Radiolabeled somatostatin analog scintigraphy in differentiated thyroid carcinoma. J Nucl Med 1995;36:807-10.
Baudin E, Schlumberger M, Lumbroso J, Travagli JP, Caillou B, Parmentier C. Octreotide scintigraphy in patients with differentiated thyroid carcinoma: Contribution for patients with negative radioiodine scan. J Clin Endocrinol Metab 1996;81:2541-4.
Ahlman H, Tisell LE, Wängberg B, Fjälling M, Forssell-Aronsson E, Kölby L, et al.
The relevance of somatostatin receptors in thyroid neoplasia. Yale J Biol Med 1997;70:523-33.
Gulec SA, Serafini AN, Sridhar KS, Peker KR, Gupta A, Goodwin WJ, et al.
Somatostatin receptor expression in Hürthle cell cancer of the thyroid. J Nucl Med 1998;39:243-5.
Garin E, Devillers A, Le Cloirec J, Bernard AM, Lescouarc'h J, Herry JY, et al.
Use of indium-111 pentetreotide somatostatin receptor scintigraphy to detect recurrent thyroid carcinoma in patients without detectable iodine uptake. Eur J Nucl Med 1998;25:687-94.
Kölby L, Wängberg B, Ahlman H, Tisell LE, Fjälling M, Forssell-Aronsson E, et al.
Somatostatin receptor subtypes, octreotide scintigraphy, and clinical response to octreotide treatment in patients with neuroendocrine tumors. World J Surg 1998;22:679-83.
Valli N, Catargi B, Ronci N, Leccia F, Guyot M, Roger P, et al.
Evaluation of indium-111 pentetreotide somatostatin receptor scintigraphy to detect recurrent thyroid carcinoma in patients with negative radioiodine scintigraphy. Thyroid 1999;9:583-9.
Haslinghuis LM, Krenning EP, De Herder WW, Reijs AE, Kwekkeboom DJ. Somatostatin receptor scintigraphy in the follow-up of patients with differentiated thyroid cancer. J Endocrinol Invest 2001;24:415-22.
Görges R, Kahaly G, Müller-Brand J, Mäcke H, Roser HW, Bockisch A. Radionuclide-labeled somatostatin analogues for diagnostic and therapeutic purposes in nonmedullary thyroid cancer. Thyroid 2001;11:647-59.
Forssell-Aronsson EB, Nilsson O, Bejegård SA, Kölby L, Bernhardt P, Mölne J, et al.
111In-DTPA-D-Phe1-octreotide binding and somatostatin receptor subtypes in thyroid tumors. J Nucl Med 2000;41:636-42.
Decristoforo C, Melendez-Alafort L, Sosabowski JK, Mather SJ. 99mTc-HYNIC-[Tyr3]-octreotide for imaging somatostatin-receptor-positive tumors: Preclinical evaluation and comparison with 111In-octreotide. J Nucl Med 2000;41:1114-9.
Decristoforo C, Mather SJ, Cholewinski W, Donnemiller E, Riccabona G, Moncayo R. 99mTc-EDDA/HYNIC-TOC: A new 99mTc-labelled radiopharmaceutical for imaging somatostatin receptor-positive tumours; first clinical results and intra-patient comparison with 111In-labelled octreotide derivatives. Eur J Nucl Med 2000;27:1318-25.
Gabriel M, Decristoforo C, Donnemiller E, Ulmer H, Watfah Rychlinski C, Mather SJ, et al.
An intrapatient comparison of 99mTc-EDDA/HYNIC-TOC with 111In-DTPA-octreotide for diagnosis of somatostatin receptor-expressing tumors. J Nucl Med 2003;44:708-16.
Sobin LH, Wittekind C. International Union Against Cancer. TNM Classification of Malignant Tumours. 5 th
ed. New York: Wiley-Liss; 1997.
American Joint Committee on Cancer. AJCC Cancer Staging Manual. 5 th
ed. In: Part II: 8. Thyroid Gland. Philadelphia, New York: Lippincott-Raven; 1997. p. 59-61.
Decristoforo C, Mather SJ. Preparation, 99mTc-labeling, and in vitro
characterization of HYNIC and N3S modified RC-160 and [Tyr3]octreotide. Bioconjug Chem 1999;10:431-8.
Le Rest C, Bomanji JB, Costa DC, Townsend CE, Visvikis D, Ell PJ. Functional imaging of malignant paragangliomas and carcinoid tumours. Eur J Nucl Med 2001;28:478-82.
Petrich T, Börner AR, Otto D, Hofmann M, Knapp WH. Influence of rhTSH on [(18) F] fluorodeoxyglucose uptake by differentiated thyroid carcinoma. Eur J Nucl Med Mol Imaging 2002;29:641-7.
Wang W, Larson SM, Tuttle RM, Kalaigian H, Kolbert K, Sonenberg M, et al.
Resistance of [18f]-fluorodeoxyglucose-avid metastatic thyroid cancer lesions to treatment with high-dose radioactive iodine. Thyroid 2001;11:1169-75.
Robbins RJ, Hill RH, Wang W, Macapinlac HH, Larson SM. Inhibition of metabolic activity in papillary thyroid carcinoma by a somatostatin analogue. Thyroid 2000;10:177-83.
Arnold R, Simon B, Wied M. Treatment of neuroendocrine GEP tumours with somatostatin analogues: A review. Digestion 2000;62 Suppl 1:84-91.
Waldherr C, Schumacher T, Pless M, Crazzolara A, Maecke HR, Nitzsche E, et al.
Radiopeptide transmitted internal irradiation of non-iodophil thyroid cancer and conventionally untreatable medullary thyroid cancer using [90Y]-DOTA-D-Phe1-Tyr3-octreotide: A pilot study. Nucl Med Commun 2001;22:673-8.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3], [Table 4]