|Year : 2020 | Volume
| Issue : 3 | Page : 266-270
30 mCi exploratory scan for two-step dosimetric131I therapy in differentiated thyroid cancer patients: A novel approach and case report
Di Wu1, Cristiane Jeyce Gomes-Lima2, Kanchan Kulkarni3, Kenneth D Burman4, Leonard Wartofsky2, Douglas Van Nostrand1
1 Medstar Health Research Institute, Hyattsville, MD; Department of Nuclear Medicine Research, Medstar Washington Hospital Center, Washington, DC, USA
2 Medstar Health Research Institute, Hyattsville, MD; Division of Endocrinology, Medstar Washington Hospital Center, Washington, DC, USA
3 Division of Nuclear Medicine, Medstar Washington Hospital Center, Washington, DC, USA
4 Division of Endocrinology, Medstar Washington Hospital Center, Washington, DC, USA
|Date of Submission||02-May-2019|
|Date of Acceptance||17-Sep-2019|
|Date of Web Publication||17-Jan-2020|
Dr. Douglas Van Nostrand
Nuclear Medicine Research, MedStar Washington Hospital Center, 110 Irving Street, NW, Washington, DC 20010
| Abstract|| |
Differentiated thyroid cancer patients with significantly elevated or rapidly rising serum thyroglobulin (Tg) levels and negative diagnostic radioiodine scans (DxScan) often present a therapeutic dilemma in deciding whether or not to administer an131I treatment. In this report, we describe a novel two-step approach of a 30 mCi131I exploratory scan before a dosimetric131I therapy to help “un-blind” the treating physician of the benefit/risk ratio of a further “blind”131I treatment. A 51-year-old man presented with rising Tg levels, a negative DxScan, and a history of widely metastatic follicular thyroid cancer. He had undergone total thyroidectomy, remnant ablation with 3.8 GBq (103.5 mCi) of131I, Gammaknife®, and treatment with 12.1 GBq (326 mCi) of131I for multiple metastases. However, at 19 months after the treatments, his Tg levels continued to rise, and scans demonstrated no evidence of radioiodine-avid metastatic disease. In anticipation of a “blind”131I treatment, the medical team and the patient opted for a 30 mCi exploratory scan. The total dosimetrically guided prescribed activity (DGPA) was decided based on the whole-body dosimetry. The patient was first given 30 mCi of131I, and the exploratory scan was performed 22 h later, which demonstrated131I uptake in the left lung, left humeral head, T10, and right proximal thigh muscle. Based on the positive exploratory scan, the remainder of the DGPA was administered within several hours after the scan. On the post-DGPA treatment scan performed at 5–7 days, the lesions seen on the ~ 22 h exploratory scan were confirmed, and an additional lesion was observed in the left kidney. The 30 mCi exploratory scan suggested the potential for a response in the radioiodine-avid lesions despite a negative diagnostic scan. This method allows131I treatment to be administered to patients who may have a greater potential for a therapeutic response while avoiding unwarranted side effects in those patients with nonavid disease.
Keywords: 131I treatment, 30 mCi exploratory scan, differentiated thyroid cancer, dosimetry, negative diagnostic scan, positive thyroglobulin
|How to cite this article:|
Wu D, Gomes-Lima CJ, Kulkarni K, Burman KD, Wartofsky L, Van Nostrand D. 30 mCi exploratory scan for two-step dosimetric131I therapy in differentiated thyroid cancer patients: A novel approach and case report. World J Nucl Med 2020;19:266-70
|How to cite this URL:|
Wu D, Gomes-Lima CJ, Kulkarni K, Burman KD, Wartofsky L, Van Nostrand D. 30 mCi exploratory scan for two-step dosimetric131I therapy in differentiated thyroid cancer patients: A novel approach and case report. World J Nucl Med [serial online] 2020 [cited 2020 Oct 30];19:266-70. Available from: http://www.wjnm.org/text.asp?2020/19/3/266/275855
| Introduction|| |
The management of differentiated thyroid cancer (DTC) patients who have positive serum thyroglobulin (Tg) levels and negative diagnostic radioiodine scans (DxScan) is problematic. The treating physician does not know whether or not a metastasis will take up radioiodine that will result in a significant therapeutic effect, and hence the physician is “blind” to the benefit/risk ratio. In these patients, one option is to administer a “blind”131 I therapy, which may result in no beneficial effect with the potential for significant side effects; however, the alternative is to not administer a “blind”131 I therapy, which may eliminate a potential therapeutic treatment for that patient.
The 2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Thyroid Cancer recommends that a “blind”131 I treatment may be considered based on the levels of serum Tg ≥10 ng/ml. However, no reliable method is available to help determine a priori whether or not a patient may benefit from a “blind”131 I treatment other than actually administering the131 I treatment itself and subsequently observing a posttherapy scan (TxScan) to assess the degree of uptake. In order to better differentiate radioiodine-avid versus nonavid disease, we propose a 30 mCi exploratory scan before a dosimetric131 I therapy as a novel empiric approach, which may help “un-blind” the treating physician. This might allow131 I treatment in more patients who could benefit from a therapeutic effect while eliminating the side effects of a “blind”131 I treatment in patients who have little or no potential benefit. This approach may be of interest in patients who are being considered for larger activities of131 I, typically determined by dosimetry.
Methodology of the 30 mCi131 I exploratory scan
A patient who has DTC, significantly elevated or rising Tg levels, and negative DxScan is informed of the risks and benefits of the various options of no treatment (e.g., active surveillance), focal treatment of structural disease, a “blind”131 I treatment, a 30 mCi131 I exploratory scan, and systemic therapy. If the patient and referring physician agree to the empirical option of a 30 mCi131 I exploratory scan, then the preparation and performance of the exploratory scan is as follows.
The patient maintains a low-iodine diet for at least 10–14 days with adequate iodine depletion assessed by the measurement of urinary iodine-to-creatinine ratio at the end of the period of low-iodine diet. The patient is prepared with either thyroid hormone withdrawal or injections of recombinant human thyroid-stimulating hormone (rhTSH). Subsequently, whole-body dosimetry is performed with 74 MBq (2 mCi) of131 I., Based on the dosimetrically calculated maximum tolerated activity (MTA) and patient history, the medical team and the patient agree upon a dosimetrically guided prescribed activity (DGPA) for the patient's possible131 I treatment. The patient is then orally administered 1.11 GBq (30 mCi) of the total131 I DGPA. Twenty-four to 36 h later, anterior and posterior whole-body images, anterior and posterior spot images of the neck and chest, and anterior pinhole collimator images of the thyroid bed are obtained. If necessary, single-photon emission computed tomography (SPECT) is performed. Appropriate radiation precautions for a prescribed activity of 1.11 GBq (30 mCi) are followed. The specifics of performing these scans and the radiation safety precautions have been previously discussed in more detail by Van Nostrand and Atkins and Vetter and Glenn, respectively. The images are promptly reviewed by the nuclear medicine physician. If the images are positive for DTC metastasis, then a decision whether or not to administer the remainder of the DGPA is taken. If the images are negative for functioning metastasis, then no further131 I is administered. Regardless of whether the patient received only 1.11 GBq (30 mCi) or the total DGPA, a TxScan is performed 5–7 days later.
The131 I activity of 1.11 GBq (30 mCi) was chosen because it used to be the highest131 I activity allowed for outpatient procedures by the United States Nuclear Regulatory Commission. This activity amount would be reasonable to choose because it would allow most imaging facilities to do the 30 mCi exploratory scan as an outpatient procedure without any further radiation safety forms that had to be completed by the patient and/or additional approval through a radiation safety committee or department.
| Case Report|| |
A 51-year-old man presented to the clinic with rising Tg levels, a negative DxScan, and a history of widely metastatic follicular thyroid cancer. Previously, he underwent total thyroidectomy with no lymph node dissection and remnant ablation with 3.8 GBq (103.5 mCi) of131 I for a 7.4 cm well-differentiated minimally invasive follicular carcinoma with no other aggressive features. At 9 months after131 I therapy, his suppressed Tg was 0.8 ng/ml (TSH not available; TgAb negative). Fourteen months later, he was found to have multiple bilateral pulmonary and liver, renal, and brain metastases with a Tg of 31 ng/ml while on thyroxine. The brain metastases were treated with Gammaknife®, and the other metastases were treated with 12.1 GBq (326 mCi) of131 I. The131 I TxScan showed radioiodine-avid bilateral pulmonary metastases, right-lobe hepatic metastases, and left humerus and right iliac crest bone metastases. For 12 months, the suppressed Tg was stable between 5.2 and 6.0 ng/ml.
However, at 14 and 19 months after the treatment, the suppressed Tg had risen from 29 ng/ml (TSH 0.64 mIU/L) to 160 ng/ml (TSH 1.01 mIU/L), and the stimulated Tg was 327 ng/ml (TSH 81 mIU/L) at 19 months. An18 F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) scan showed new lesions in the left side of T10 and left suprascapular muscle. A rhTSH stimulated 74 MBq (2 mCi)131 I DxScan, with TSH 80.74 mIU/L and urinary iodine-to-creatinine ratio 38.7 mg/g, demonstrated no evidence of radioiodine-avid metastatic disease [Figure 1], and a “blind” treatment was considered.
|Figure 1: Negative diagnostic131I scan. The thyrogen-stimulated 74 MBq (2 mCi)131I diagnostic radioiodine scans imaged at 48 h demonstrated no evidence of radioiodine-avid metastatic disease. Thyroid-stimulating hormone stimulation was adequate at thyroid-stimulating hormone 80.74 mIU/L, and low-iodine diet decreased urinary iodine-to-creatinine ratio to 38.7 μg/g|
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In anticipation of a “blind”131 I treatment, the medical team and the patient opted for a 30 mCi exploratory scan. A whole-body dosimetry was performed, and the calculated MTA was 27.2 GBq (735 mCi), of which the medical team agreed on a total DGPA of 12.2 GBq (330 mCi). After the intramuscular injection of 0.9 mg of rhTSH on 2 consecutive days, the patient was given 28.6 mCi of131 I on the next day. Approximately 22 h later, the exploratory scan was performed and demonstrated131 I uptake in the left lung, left humeral head, T10, and right proximal thigh muscle [Figure 2]a. The remainder of the DGPA (i.e., 11.0 GBq [298 mCi]) of131 I was administered within several hours after the scan. On the post-DGPA TxScan and SPECT/CT performed at 6 days (138.5 h), the lesions seen on the ~22 h exploratory scan were confirmed, and an additional lesion was observed in the left kidney [Figure 2]b. These images suggested the potential for a response in the radioiodine-avid lesions; however, no long-term follow-up data are presently available.
|Figure 2: Positive 30 mCi exploratory scan and positive postdosimetrically guided prescribed activity scan. (a) A positive “30 mCi exploratory scan” performed at ~22 h after administration of 28.6 mCi of131I demonstrated abnormal131I uptake in the lung, bone, and muscle. The patient was administered the remainder of the planned dosimetrically guided prescribed activity. (b) It was performed 6 days (138.5 h) after the administration of the dosimetrically guided prescribed activity and demonstrated the previous uptake and new uptake in the left kidney. Additional single-photon emission computed tomography/computed tomography (nondiagnostic computed tomography scan for anatomic localization only) showed discrete abnormal focal uptake at T10-T11 vertebrae, discrete abnormal focal uptake co-registered to the right kidney, and smaller but discrete focal uptake co-registered to the left kidney, which was a left renal cyst|
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| Discussion|| |
This report presents a novel approach – “the 30 mCi131 I exploratory scan” – that offers an option to potentially “un-blind” the treating physician and help better determine which patients may benefit from131 I treatment, while helping to avoid131 I treatment and its potential side effects in patients who may have little or no benefit. Management is often problematic for DTC patients who have significantly elevated or rising serum Tg and negative DxScans. Several studies have shown that depending on the patient cohort and the imaging technique, as many as 13%–64% of patients with negative DxScans have uptake in at least some of the metastatic lesions on an131 I TxScan.,, Even in patients with negative124 I pretherapy PET/CT, Khorjekar et al., Lammers et al., and Kist et al. have observed that 83% (10/12), 83% (5/6), and 33% (4/12) of patients will have a positive131 I TxScan, respectively.
Although patients with a negative 30 mCi exploratory scan may have a positive exploratory scan if higher131 I activities are administered for imaging, we do not recommend this. We submit that even if a metastasis was positive on an exploratory scan performed with a higher131 I activity, it may have a lower likelihood of achieving a meaningful therapeutic effect.
However, the 30 mCi exploratory scan has multiple limitations. First,131 I uptake seen on the 30 mCi exploratory scan may be indicative of radioiodine-avid metastases, but it does not necessarily indicate that a significant therapeutic effect will result from the131 I treatment. Chao systematically reviewed 17 studies with a total of 337 Tg+/DxScan- patients who received an empiric “blind”131 I therapy of 2.8–11.1 GBq (75–300 mCi) and found that 62% had a positive TxScan and 20% (66/337) did not have significant decrease in Tg levels. Structural response was not evaluated in their review. Nevertheless, as patients with a significantly elevated or rapidly rising Tg typically have significant progressive disease with a poor prognosis and few remaining treatment options, it may be premature to dismiss131 I as a treatment option based on a negative low activity (e.g., 37–185 MBq [1–5 mCi]) DxScan. Although the likelihood of a good response to131 I treatment is lower in these patients, the possibility exists that131 I treatment may be beneficial, at least for some lesions, and this option should be explored prior to considering targeted systemic therapy or immunotherapy. The 30 mCi exploratory scan offers that possibility. A second limitation of a 30 mCi exploratory scan is the possibility of stunning or partial treatment. McDougall has suggested that stunning most likely occurs several days (i.e., ~48–72 h) after131 I administration., In our patient, the remainder of the DGPA was given ~24 h after administering 30 mCi, which we believe decreases the likelihood of stunning. In addition, the 5–7 day TxScan demonstrated uptake in those lesions that were visualized at ~24 h, which also argues against stunning, but it does not exclude the possibility of some stunning. Similarly, even if the lesions were not visualized on a TxScan, that does not necessarily indicate stunning; it may depend on other factors such as relative rates of uptake and clearance of the tumor and/or background. Salvatori et al. evaluated TxScans and showed that scans performed at 3 days after131 I treatment missed 12% (16/134) of all lesions seen on either the 3-day or the 7-day scan, and scans performed at 7 days after131 I treatment missed 7.5% (10/134) of all lesions. A third limitation is that the remainder of the DGPA was given ~48 h after the second injection of rhTSH; this could potentially reduce the uptake of the131 I activity as the TSH levels are rapidly declining. In addition, the pharmacokinetics of thyrotropin alfa were studied in 16 DTC patients to show that TSH level reached a mean peak of 116 ± 38 mIU/L at 3–24 h and the mean half-life was 25 ± 10 h after a single intramuscular dose of 0.9 mg. Duntas et al. performed serial TSH measurements in seven DTC patients and showed that the TSH level at 48 h after the second thyrotropin alfa injection was above 25–30 mIU/L, which has been proposed as sufficient for131 I treatment.
| Conclusion|| |
We report on the 30 mCi exploratory scan as a novel method to facilitate the decision whether or not to administer131 I treatment to a patient who has a significantly elevated or rapidly rising Tg and a negative DxScan. Although this novel approach will not be infallible in predicting which patients will or will not benefit from an131 I treatment, it provides an option for potentially safer and better management of these patients.
This study was underwritten by donations from patients.
Consent for publication
Consent to publish the case was obtained from the individual in this case report.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient understands that his name and initials will not be published, and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Wartofsky L. Management of the patients with negative radioiodine scan and elevated serum thyroglobulin. In: Wartofsky L, Van Nostrand D, editors. Thyroid Cancer: A Comprehensive Guide to Clinical Management. New York: Springer; 2016. p. 529-38.
Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al.
2015 American Thyroid Association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: The American Thyroid Association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid 2016;26:1-33.
Van Nostrand D, Atkins F, Yeganeh F, Acio E, Bursaw R, Wartofsky L. Dosimetrically determined doses of radioiodine for the treatment of metastatic thyroid carcinoma. Thyroid 2002;12:121-34.
Atkins FB, Van Nostrand D, Wartofsky L. Dosimetrically determined prescribed activity of 131i for the treatment of metastatic differentiated thyroid carcinoma. In: Wartofsky L, van Nostrand D, editors. Thyroid Cancer: A Comprehensive Guide to Clinical Management. New York: Springer; 2016. p. 635-50.
Atkins FB, Van Nostrand D. Radioiodine whole-body imaging. In: Wartofsky L, Van Nostrand D, editors. Thyroid Cancer: A Comprehensive Guide to Clinical Management. New York: Springer; 2016. p. 133-52.
Vetter RJ, Glenn J. Radiation and radioactivity. In: Wartofsky L, Van Nostrand D, editors. Thyroid Cancer: A Comprehensive Guide to Clinical Management. New York: Springer; 2016. p. 585-93.
Wells K, Moreau S, Shin YR, Van Nostrand D, Burman K, Wartofsky L. Positive (+) post-treatment (tx) scans after the radioiodine (RAI) tx of patients who have well-differentiated thyroid cancer (WDTC), positive serum thyroglobulin levels (TG+), and negative diagnostic (dx) RAI whole body scans (WBS-): Predictive values and frequency. J Nucl Med 2008;49 Suppl 1:238P.
Wells K, Moreau S, Shin YR, Aiken M, Van Nostrand D, Burman K, et al
. To treat or not to treat “thyroglobulin-positive and radioiodine diagnostic whole body scan negative” patients with well-differentiated thyroid cancer: An educational exhibit. J Nucl Med 2008;49 Suppl 1:180P.
Khorjekar GR, Van Nostrand D, Garcia C, O'Neil J, Moreau S, Atkins FB, et al.
Do negative 124I pretherapy positron emission tomography scans in patients with elevated serum thyroglobulin levels predict negative 131I posttherapy scans? Thyroid 2014;24:1394-9.
Lammers GK, Esser JP, Pasker PC, Sanson-van Praag ME, de Klerk JM. Can I-124 PET/CT predict pathological uptake of therapeutic dosages of radioiodine (I-131) in differentiated thyroid carcinoma? Adv J Mol Imaging 2014;4:27.
Kist JW, de Keizer B, van der Vlies M, Brouwers AH, Huysmans DA, van der Zant FM, et al.
124I PET/CT to predict the outcome of blind 131I treatment in patients with biochemical recurrence of differentiated thyroid cancer: Results of a multicenter diagnostic cohort study (THYROPET). J Nucl Med 2016;57:701-7.
Chao M. Management of differentiated thyroid cancer with rising thyroglobulin and negative diagnostic radioiodine whole body scan. Clin Oncol (R Coll Radiol) 2010;22:438-47.
McDougall IR. Stunning is not a problem. In: Wartofsky L, Van Nostrand D, editors. Thyroid Cancer: A Comprehensive Guide to Clinical Management. New York: Springer; 2016. p. 237-41.
Park HM, Gerard SK. Stunning by 131i scanning: untoward effect of 131i thyroid imaging prior to radioablation therapy. In: Wartofsky L, Van Nostrand D, editors. Thyroid Cancer: A Comprehensive Guide to Clinical Management. New York: Springer; 2016. p. 225-35.
Salvatori M, Perotti G, Villani MF, Mazza R, Maussier ML, Indovina L, et al.
Determining the appropriate time of execution of an I-131 post-therapy whole-body scan: Comparison between early and late imaging. Nucl Med Commun 2013;34:900-8.
Duntas LH, Tsakalakos N, Grab-Duntas B, Kalarritou M, Papadodima E. The use of recombinant human thyrotropin (Thyrogen) in the diagnosis and treatment of thyroid cancer. Hormones (Athens) 2003;2:169-74.
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