Skip to main content

Main menu

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Corporate & Special Sales
    • Journal Claims
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Permissions
    • Advertisers
    • Continuing Education
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI

User menu

  • Subscribe
  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Nuclear Medicine
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI
  • Subscribe
  • My alerts
  • Log in
  • My Cart
Journal of Nuclear Medicine

Advanced Search

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Corporate & Special Sales
    • Journal Claims
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Permissions
    • Advertisers
    • Continuing Education
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • Follow JNM on Twitter
  • Visit JNM on Facebook
  • Join JNM on LinkedIn
  • Subscribe to our RSS feeds
Research ArticleClinical Investigations

High Level of Agreement Between Pretherapeutic 124I PET and Intratherapeutic 131I Imaging in Detecting Iodine-Positive Thyroid Cancer Metastases

Marcus Ruhlmann, Walter Jentzen, Verena Ruhlmann, Cinzia Pettinato, Gloria Rossi, Ina Binse, Andreas Bockisch and Sandra Rosenbaum-Krumme
Journal of Nuclear Medicine September 2016, 57 (9) 1339-1342; DOI: https://doi.org/10.2967/jnumed.115.169649
Marcus Ruhlmann
1Department of Nuclear Medicine, University Hospital, University Duisburg-Essen, Essen, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Walter Jentzen
1Department of Nuclear Medicine, University Hospital, University Duisburg-Essen, Essen, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Verena Ruhlmann
1Department of Nuclear Medicine, University Hospital, University Duisburg-Essen, Essen, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Cinzia Pettinato
2Medical Physics Unit, Orsola-Malpighi University Hospital, Bologna, Italy; and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Gloria Rossi
3Medical Physics Unit, Service Department, Macerata Hospital, Macerata, Italy
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Ina Binse
1Department of Nuclear Medicine, University Hospital, University Duisburg-Essen, Essen, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Andreas Bockisch
1Department of Nuclear Medicine, University Hospital, University Duisburg-Essen, Essen, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Sandra Rosenbaum-Krumme
1Department of Nuclear Medicine, University Hospital, University Duisburg-Essen, Essen, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

The aim of this retrospective study was to assess the level of agreement between PET and scintigraphy using diagnostic amounts of 124I and therapeutic amounts of 131I, respectively, in detecting iodine-positive metastases in patients with differentiated thyroid carcinoma. Methods: The study included patients who underwent PET/CT 24 and 120 h after administration of approximately 25 MBq of 124I and subsequently underwent imaging 5–10 d after administration of 1–10 GBq of 131I. For each patient, the intratherapeutic 131I imaging comprised a whole-body scintigraphy scan and a SPECT/CT scan of the neck to distinguish between metastatic and thyroid remnant tissues. Iodine uptake was rated as a metastatic focus if located outside the thyroid bed. Lesion- and patient-based analyses were performed. Results: The study included 137 patients with 227 metastases iodine-positive on both functional imaging modalities. In the lesion-based analysis, 124I PET and 131I imaging detected 98% (223/227) and 99% (225/227) of the iodine-positive metastases, respectively; the level of agreement between 124I PET and 131I imaging was 97% (221/227). Four metastases (3 lymph node and 1 bone) in 4 patients were 124I-negative but 131I-positive, and 2 lymph node metastases in 2 patients were 131I-negative but 124I-positive. In the patient-based analysis, 61 of the 137 patients presented with iodine-positive metastases. 124I PET and 131I imaging detected at least one iodine-positive metastasis in 97% (59/61) and 98% (60/61) of the patients, respectively. The level of agreement was 95% (58/61). Both imaging modalities concordantly identified 76 of 137 patients without pathologic iodine uptake. Conclusion: Because of the high level of agreement, pretherapeutic 124I PET/CT is an adequate methodology in the detection of iodine-positive metastases and can be used as a reliable tool for staging of thyroid cancer patients and individualized treatment planning.

  • 124I PET/CT
  • SPECT/CT
  • whole-body scintigraphy
  • thyroid cancer
  • radioiodine therapy

Radioiodine therapy is an integral component in the treatment of differentiated thyroid cancer. The identification of iodine-positive metastases is crucial for therapy planning and patient management. The sensitivity for detecting metastases depends on the characteristics of not only the radioiodine isotopes but also the imaging device.

Over the last decade, the use of the positron-emitting 124I, with diagnostic activities of 20–80 MBq, has become more frequent in staging (1–7) and in pretherapeutic dosimetry to estimate the absorbed doses of iodine-positive foci and of organs at risk in order to optimize radioiodine therapy (7–13). The more frequent use of 124I is related mainly to the higher scanner efficiency of 124I PET/CT, the higher sensitivity for detection of iodine-positive foci when similar amounts of diagnostic activities are applied, and the higher quantitative capacity relative to 131I whole-body scintigraphy (WBS) or SPECT/CT (4,5,14). Especially in high-risk patients, pretherapeutic 124I PET/CT, either as part of a dosimetry approach or for imaging only, was found beneficial in detecting local and distant metastases and altered therapy management (2,4,6,7,9–11). Moreover, 124I PET/CT has been mentioned in European and American guidelines (15,16).

However, a recent study by Lammers et al. (17) cast doubt on the benefit of 124I PET/CT—compared with intratherapeutic 131I imaging—in the detection of iodine-positive metastases. Lammers et al. reported that in a significant number of patients, PET/CT using a tracer amount (40 MBq) of 124I failed to predict the uptake in metastatic tissue observed on intratherapeutic scintigraphy performed 7 d after administration of 3.7–7.4 GBq of 131I. This finding of poor sensitivity in detecting iodine-positive metastases heavily contradicts the clinical experience and current literature (7,10).

For over a decade, we have been routinely applying 124I PET with or without CT in high-risk differentiated thyroid cancer patients, including for pretherapeutic dosimetry to estimate the individual optimized therapeutic radioiodine activity. On the basis of these data, we analyzed the level of agreement between 124I PET and intratherapeutic 131I imaging in detecting iodine-positive metastases in a large patient cohort.

MATERIALS AND METHODS

Patients

All patients gave written informed consent, and the local medical research ethics committee approved the study. The study consisted of patients who underwent serial 124I PET/CT (as part of the pretherapeutic dosimetry protocol) and, several days after the last 124I PET/CT scan, radioiodine therapy that included intratherapeutic 131I imaging. The patients were asked to maintain a low-iodine diet for at least 4 wk before the examinations (verified by a urinary iodine level < 250 μg/g creatinine).

In total, 137 patients with differentiated thyroid cancer were included (110 with papillary carcinoma, 20 with follicular carcinoma, and 7 with poorly differentiated carcinoma). At the time of dosimetry, the mean age of the patients (90 female and 47 male) was 50 y (median, 51 y; range, 12–85 y). 124I PET/CT dosimetry and radioiodine therapy were performed during hormone withdrawal (n = 133) or with recombinant thyroid-stimulating hormone (n = 4). In all cases, the serum thyroid-stimulating hormone value was at least 30 mU/L.

Of the 137 patients, 106 underwent dosimetry 4 wk after thyroidectomy as a means of initial diagnosis because they were at high risk of differentiated thyroid cancer. In the remaining 31 patients, dosimetry was performed for tumor localization because of an increasing level of serum thyroglobulin or for evaluation of indistinct findings during the first radioiodine therapy. These 31 patients had already undergone 1.4 radioiodine treatments on average (median, 1; range, 1–6), with a mean applied cumulative activity of 6.7 GBq of 131I (median, 3.0 GBq; range, 1.0–47.0 GBq) and a mean thyroglobulin level of 528 ng/mL (median, 16.0 ng/mL; range, 0.0–9304 ng/mL).

Pretherapeutic 124I PET/CT

PET/CT was performed 24 and 120 h after oral administration of a mean 124I activity of 24.1 MBq (median, 24.3 MBq; range, 20.2–28.5 MBq) according to our dosimetry protocol (8,12). It was expected that this low activity would not cause a significant stunning effect. The images were acquired on a Biograph Duo PET/CT scanner (Siemens Medical Solutions). The examinations included whole-body PET/CT scans from head to thigh using 5–8 bed positions. PET/CT scanning started with a spiral CT scan using low-dose technique (tube voltage, 110 kVp; tube current–time product, 15 mAs; beam pitch, 2.0; slice width, 5 mm; collimation, 4 mm; table feed, 16 mm). No contrast agent was applied. Subsequently, a PET scan was acquired with an emission time of 240 s per bed position.

After Fourier rebinning, the PET images were reconstructed using attenuation-weighted ordered-subset expectation maximization. Standard corrections for random coincidences, dead time, and scatter were performed. The images were corrected for attenuation using a CT-based method. For image assessment, the standard image reconstruction parameters were 2 iterations and 8 subsets, a postreconstruction 3-dimensional gaussian smoothing filter of 5 mm, and a reconstructed voxel size of 5.2 × 5.2 × 2.4 mm. The CT images were reconstructed with a voxel size of 1.0 × 1.0 × 5.0 mm and the standard reconstruction kernel, B30f.

Intratherapeutic 131I Imaging

We prefer using the term intratherapeutic imaging instead of posttherapeutic imaging to avoid confusion with follow-up imaging. The intratherapeutic WBS was performed 5–10 d after radioiodine therapy (mean 131I activity, 4.4 GBq; median, 3.0 GBq; range, 1.0–10.0 GBq) using a double-head γ-camera (Symbia S; Siemens) equipped with a high-energy, parallel-hole collimator. The table speed was 15 cm/min. The matrix was 256 × 1,024, resulting in 2.4 × 2.4 mm pixels.

All patients underwent SPECT/CT of the neck on a scanner (Symbia T2; Siemens) equipped with a high-energy, parallel-hole collimator. Low-dose CT for attenuation correction was performed without a contrast agent (tube voltage, 130 kVp; tube current–time product, 17 mAs; beam pitch, 1.5; slice width, 5 mm). The SPECT scan was acquired using 128 angles over 360° and 25 s per stop. Images were iteratively reconstructed and corrected for attenuation and scatter (Flash 3D [Siemens], 4 subsets and 8 iterations; gaussian intersliced smoothing filter; attenuation coefficient, 0.15 cm−1). The image matrix was 128 × 128, resulting in a cuboid voxel length of 4.8 mm.

Lesion- and Patient-Based Analyses

Four experienced nuclear physicians separately interpreted the 124I PET/CT, 131I WBS, and 131I SPECT/CT images in different sessions and with masking to each other. The findings derived from PET images were compared with the findings derived from 131I images. In cases of different observer ratings, a consensus was obtained in an additional session. A focus of iodine uptake was classified as metastatic tissue if located outside the thyroid bed. Iodine-positive foci within the thyroid bed were classified as probable thyroid remnants and were not included. Lesion- and patient-based analyses were performed to assess the findings derived from 124I PET and 131I images. Foci were considered positive on 124I PET if they were evident on early or late images.

The lesion-based analysis counted the total number of iodine-positive foci detected by both functional imaging modalities together. The level of agreement regarding concordantly detected foci on 124I PET and 131I images was determined. Some patients had multiple pulmonary and osseous metastases. In these cases, the number of pulmonary or osseous foci was restricted to 7 in each patient to avoid selection bias. The limit of 7 foci was selected because, in the other patients, the highest number of distinguishable lung or bone metastases was 7 in one patient. The maximum signal and the signal-to-background ratios of the discordant foci were derived from the images.

The patient-based analysis counted the number of iodine-positive patients detected by both functional imaging modalities together. The level of agreement regarding iodine-positive patients observed in each modality was determined.

RESULTS

In total, 227 metastases (91 lymph node, 76 lung, 55 bone, and 5 other tissue) were detected by the imaging modalities together. Seven or more pulmonary metastases and bone metastases were found in 8 patients and 5 patients, respectively. 124I PET alone detected 223 metastases (98%), and 131I imaging alone detected 225 (99%). The level of agreement between 124I PET and 131I imaging was 97% (221/227). Some properties of the 6 discordant foci, in 6 patients, are listed in Table 1. Four (foci 1–4) were before the first radioiodine treatment, and 2 (foci 5 and 6) were after radioiodine treatment. Two lymph node metastases (foci 1 and 2) were negative on 131I imaging but positive on 124I PET. Three lymph node metastases (foci 3, 4, and 6) and 1 bone metastasis (focus 5) in 4 patients were 124I-negative but 131I-positive. Figures 1 and 2 show foci 1 and 5, which were detected only on 124I PET/CT and 131I imaging, respectively.

View this table:
  • View inline
  • View popup
TABLE 1

Properties of Discordant Metastases, Administered Therapeutic Activities, and Time Point of 131I Images

FIGURE 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIGURE 1.

Patient with iodine-positive right nuchal lymph node metastasis (focus 1, arrows) detected by early 124I PET/CT but not by 131I SPECT/CT. Shown are axial cervical SPECT (A) and SPECT/CT (B) images, along with their corresponding PET (C) and PET/CT (D) images.

FIGURE 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIGURE 2.

Patient with iodine-positive rib metastasis (focus 5, white arrows) detected not by maximum-intensity-projection 124I PET (A) but by planar 131I WBS (B) and axial SPECT/CT (C). Black arrows mark iodine-positive left scapula metastasis, and gray arrows lower lumbar spine metastasis.

In the patient-based analysis, 61 patients were categorized as iodine-positive: 59 (97%) on 124I PET and 60 (98%) on 131I imaging. The level of agreement between 124I PET and 131I imaging was 95% (58/61). Seventy-six patients were concordantly found to be without iodine-positive metastases by both imaging modalities.

DISCUSSION

Two published studies have found that after administration of radioiodine for diagnostic purposes, a higher number of iodine-positive foci are detected by 124I PET than by 131I WBS (4,5). The activity used in these studies varied between 63–74 MBq of 124I (4) and 37–74 MBq of 131I (5). Consequently, 124I PET is considered the favored diagnostic tool for detection of metastatic foci. Several studies have also shown the superiority of 124I PET over intratherapeutic 131I imaging after application of a therapeutic amount of 131I activity (1,7,9). However, other studies (17,18) have found that 124I PET may be inferior.

The present study demonstrated, in a large patient cohort (including radioiodine-naive patients and patients previously treated with radioiodine), a high level of lesion-based and patient-based agreement between diagnostic 124I PET and intratherapeutic 131I imaging. Of the 227 metastases found in 61 patients, only 6 iodine-positive metastases (foci 1–6) in 6 patients (Table 1) were discordantly detected. A possible explanation for foci 1 and 2 is that they were detected on 124I PET/CT but not on 131I WBS after therapeutic radioiodine application because of the fast iodine kinetics and the late time points (10 d and 7 d) of WBS. Regarding focus 6, it might have been observed only on 131I images because of the high therapeutic activity, 10 GBq. Detection of the other 3 metastases (foci 3–5) only on 131I images might have been due to slow iodine kinetics.

The findings of the present study are in contrast to those of recently published studies (17,18). Lammers et al. analyzed 30 patients, and their Table 1 indicates that only 7 of them underwent subsequent radioiodine treatment (17). The 124I PET/CT results for the other 23 patients were compared with the results of noniodine imaging, such as CT or sonography, and with thyroglobulin values. Thus, a statement to a reliable detection of iodine uptake in metastases with 124I PET/CT compared with noniodine imaging is inappropriate because the presence of iodine-negative lesions, especially in metastatic patients with long-term follow-up, is well known. Khorjekar et al., who also performed a patient-based assessment, reported that 124I PET yielded 124I-positive metastases in only 2 of 12 patients with 131I-positive lesions (18). However, the authors could not explain the low number of 124I-positive findings and mentioned that their patient population was narrowly selected: patients after initial 131I therapy with iodine-positive lesions and elevated thyroglobulin levels. Thus, as stated by the authors, their results should not be generalized to a different patient population. Moreover, when we juxtaposed study designs, technical factors, and patient populations, we did not find any relevant characteristics that might lead to higher lesion detection with 124I PET/CT in our study than in the studies of Lammers et al. and Khorjekar et al.

Finally, we should note that the high level of agreement in the present study could be explained by a simplistic approach. There are two main counteracting effects that have to be considered: the high therapeutic radioiodine activity and the superior scanner technology of PET/CT. In this study, applying about 30 MBq of 124I and a median of 3,000 MBq of 131I, and assuming equal pre- and intratherapeutic iodine kinetics and neglecting physical half-life differences between 124I and 131I, the total amount of uptake in metastases was approximately 100 times larger for 131I than for 124I. However, this advantage is nullified by the lower detection limit of scintigraphic systems. Our working group recently reported that a 124I uptake of approximately 0.001% can be considered the detection limit for a 1-mL focus using 25 MBq of 124I (19). In 131I scintigraphy, it has been shown that the detection limit for a focus in the neck is also approximately 0.001% for therapeutic activities, which are approximately 100 times larger than the diagnostic activity (20). Taken together, a diagnostic activity of approximately 1% of the therapeutic activity may be sufficient to achieve a high level of agreement between 124I PET/CT and 131I WBS, including SPECT/CT.

CONCLUSION

As demonstrated in our large patient population, 124I PET/CT is reliable in detecting iodine-positive metastases and provides in overall good match with intratherapeutic 131I imaging (WBS and SPECT/CT of the neck). 124I PET/CT can be used for individualized treatment planning and staging in thyroid cancer patients.

DISCLOSURE

The costs of publication of this article were defrayed in part by the payment of page charges. Therefore, and solely to indicate this fact, this article is hereby marked “advertisement” in accordance with 18 USC section 1734. No potential conflict of interest relevant to this article was reported.

Footnotes

  • Published online May 5, 2016.

  • © 2016 by the Society of Nuclear Medicine and Molecular Imaging, Inc.

REFERENCES

  1. 1.↵
    1. Freudenberg LS,
    2. Antoch G,
    3. Jentzen W,
    4. et al
    . Value of 124I-PET/CT in staging of patients with differentiated thyroid cancer. Eur Radiol. 2004;14:2092–2098.
    OpenUrlCrossRefPubMed
  2. 2.↵
    1. Freudenberg LS,
    2. Jentzen W,
    3. Görges R,
    4. et al
    . 124I-PET dosimetry in advanced differentiated thyroid cancer: therapeutic impact. Nuklearmedizin. 2007;46:121–128.
    OpenUrlPubMed
  3. 3.
    1. Freudenberg LS,
    2. Antoch G,
    3. Frilling A,
    4. et al
    . Combined metabolic and morphologic imaging in thyroid carcinoma patients with elevated serum thyroglobulin and negative cervical ultrasonography: role of 124I-PET/CT and FDG-PET. Eur J Nucl Med Mol Imaging. 2008;35:950–957.
    OpenUrlCrossRefPubMed
  4. 4.↵
    1. Phan HTT,
    2. Jager PL,
    3. Paans AMJ,
    4. et al
    . The diagnostic value of 124I-PET in patients with differentiated thyroid cancer. Eur J Nucl Med Mol Imaging. 2008;35:958–965.
    OpenUrlCrossRefPubMed
  5. 5.↵
    1. Van Nostrand D,
    2. Moreau S,
    3. Bandaru VV,
    4. et al
    . 124I positron emission tomography versus 131I planar imaging in the identification of residual thyroid tissue and/or metastasis in patients who have well-differentiated thyroid cancer. Thyroid. 2010;20:879–883.
    OpenUrlCrossRefPubMed
  6. 6.↵
    1. Lee J,
    2. Nah KY,
    3. Kim RM,
    4. et al
    . Effectiveness of [124I]-PET/CT and [18F]-FDG-PET/CT for localizing recurrence in patients with differentiated thyroid carcinoma. J Korean Med Sci. 2012;27:1019–1026.
    OpenUrlCrossRefPubMed
  7. 7.↵
    1. de Pont C,
    2. Halders S,
    3. Bucerius J,
    4. Mottaghy F,
    5. Brans B
    . 124I PET/CT in the pretherapeutic staging of differentiated thyroid carcinoma: comparison with posttherapy 131I SPECT/CT. Eur J Nucl Med Mol Imaging. 2013;40:693–700.
    OpenUrlCrossRefPubMed
  8. 8.↵
    1. Jentzen W,
    2. Freudenberg L,
    3. Eising EG,
    4. Sonnenschein W,
    5. Knust J,
    6. Bockisch A
    . Optimized 124I PET dosimetry protocol for radioiodine therapy of differentiated thyroid cancer. J Nucl Med. 2008;49:1017–1023.
    OpenUrlAbstract/FREE Full Text
  9. 9.↵
    1. Capoccetti F,
    2. Criscuoli B,
    3. Rossi G,
    4. Ferretti F,
    5. Manni C,
    6. Brianzoni E
    . The effectiveness of 124I PET/CT in patients with differentiated thyroid cancer. Q J Nucl Med Mol Imaging. 2009;53:536–545.
    OpenUrlPubMed
  10. 10.↵
    1. Pettinato C,
    2. Monari F,
    3. Nanni C,
    4. et al
    . Usefulness of 124I PET/CT imaging to predict absorbed doses in patients affected by metastatic thyroid cancer and treated with 131I. Q J Nucl Med Mol Imaging. 2012;56:509–514.
    OpenUrlPubMed
  11. 11.↵
    1. Pettinato C,
    2. Spezi E,
    3. Nanni C,
    4. et al
    . Pretherapeutic dosimetry in patients affected by metastatic thyroid cancer using 124I PET/CT sequential scans for 131I treatment planning. Clin Nucl Med. 2014;39:e367–e374.
    OpenUrlCrossRefPubMed
  12. 12.↵
    1. Jentzen W,
    2. Bockisch A,
    3. Ruhlmann M
    . Assessment of simplified blood dose protocols for the estimation of the maximum tolerable activity in thyroid cancer patients undergoing radioiodine therapy using iodine-124. J Nucl Med. 2015;56:832–838.
    OpenUrlAbstract/FREE Full Text
  13. 13.↵
    1. Jentzen W,
    2. Moldovan AS,
    3. Ruhlmann M,
    4. Görges R,
    5. Bockisch A,
    6. Rosenbaum-Krumme S
    . Lowest effective 131I activity for thyroid remnant ablation of differentiated thyroid cancer patients: dosimetry-based model for estimation. Nuklearmedizin. 2015;54:137–143.
    OpenUrl
  14. 14.↵
    1. Jentzen W,
    2. Freudenberg L,
    3. Bockisch A
    . Quantitative imaging of 124I with PET/CT in pretherapy lesion dosimetry: effects impairing image quantification and their corrections. Q J Nucl Med Mol Imaging. 2011;55:21–43.
    OpenUrlPubMed
  15. 15.↵
    1. Luster M,
    2. Clarke SE,
    3. Dietlein M,
    4. et al
    . Guidelines for radioiodine therapy of differentiated thyroid cancer. Eur J Nucl Med Mol Imaging. 2008;35:1941–1959.
    OpenUrlCrossRefPubMed
  16. 16.↵
    1. Haugen BR,
    2. Alexander EK,
    3. Bible KC,
    4. et al
    . 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;26:1–133.
    OpenUrlCrossRefPubMed
  17. 17.↵
    1. Lammers GK,
    2. Esser JP,
    3. Pasker PCM,
    4. Sanson-van Praag ME,
    5. de Klerk JMH
    . Can I-124 PET/CT predict pathological uptake of therapeutic dosages of radioiodine (I-131) in differentiated thyroid carcinoma? Adv J Mol Imaging. 2014;4:27–34.
    OpenUrlCrossRef
  18. 18.↵
    1. Khorjekar GR,
    2. Van Nostrand D,
    3. Garcia C,
    4. et al
    . Do negative 124I pretherapy positron emission tomography scans in patients with elevated serum thyroglobulin levels predict negative 131I posttherapy scans? Thyroid. 2014;24:1394–1399.
    OpenUrlCrossRefPubMed
  19. 19.↵
    1. Jentzen W,
    2. Hoppenbrouwers J,
    3. van Leeuwen P,
    4. et al
    . Assessment of lesion response in the initial radioiodine treatment of differentiated thyroid cancer using 124I PET imaging. J Nucl Med. 2014;55:1759–1765.
    OpenUrlAbstract/FREE Full Text
  20. 20.↵
    1. Hänscheid H,
    2. Lassmann M,
    3. Buck AK,
    4. Reiners C,
    5. Verburg FA
    . The limit of detection in scintigraphic imaging with I-131 in patients with differentiated thyroid carcinoma. Phys Med Biol. 2014;59:2353–2368.
    OpenUrlCrossRefPubMed
  • Received for publication November 23, 2015.
  • Accepted for publication March 26, 2016.
PreviousNext
Back to top

In this issue

Journal of Nuclear Medicine: 57 (9)
Journal of Nuclear Medicine
Vol. 57, Issue 9
September 1, 2016
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on Journal of Nuclear Medicine.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
High Level of Agreement Between Pretherapeutic 124I PET and Intratherapeutic 131I Imaging in Detecting Iodine-Positive Thyroid Cancer Metastases
(Your Name) has sent you a message from Journal of Nuclear Medicine
(Your Name) thought you would like to see the Journal of Nuclear Medicine web site.
Citation Tools
High Level of Agreement Between Pretherapeutic 124I PET and Intratherapeutic 131I Imaging in Detecting Iodine-Positive Thyroid Cancer Metastases
Marcus Ruhlmann, Walter Jentzen, Verena Ruhlmann, Cinzia Pettinato, Gloria Rossi, Ina Binse, Andreas Bockisch, Sandra Rosenbaum-Krumme
Journal of Nuclear Medicine Sep 2016, 57 (9) 1339-1342; DOI: 10.2967/jnumed.115.169649

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
High Level of Agreement Between Pretherapeutic 124I PET and Intratherapeutic 131I Imaging in Detecting Iodine-Positive Thyroid Cancer Metastases
Marcus Ruhlmann, Walter Jentzen, Verena Ruhlmann, Cinzia Pettinato, Gloria Rossi, Ina Binse, Andreas Bockisch, Sandra Rosenbaum-Krumme
Journal of Nuclear Medicine Sep 2016, 57 (9) 1339-1342; DOI: 10.2967/jnumed.115.169649
Twitter logo Facebook logo LinkedIn logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Bookmark this article

Jump to section

  • Article
    • Abstract
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • CONCLUSION
    • DISCLOSURE
    • Footnotes
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • PDF

Related Articles

  • This Month in JNM
  • PubMed
  • Google Scholar

Cited By...

  • Individualized Dosimetry for Theranostics: Necessary, Nice to Have, or Counterproductive?
  • PET Imaging for Endocrine Malignancies: From Woe to Go
  • Google Scholar

More in this TOC Section

  • Diagnostic Performance of 124I-Metaiodobenzylguanidine PET/CT in Patients with Pheochromocytoma
  • Effects of Tracer Uptake Time in Non–Small Cell Lung Cancer 18F-FDG PET Radiomics
  • Nuclear Imaging for Classic Fever of Unknown Origin: Meta-Analysis
Show more CLINICAL INVESTIGATIONS

Similar Articles

Keywords

  • 124I PET/CT
  • SPECT/CT
  • whole-body scintigraphy
  • Thyroid cancer
  • radioiodine therapy
SNMMI

© 2023 Journal of Nuclear Medicine

Powered by HighWire