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LetterLetters to the Editor

Reply: THYROPET Study: Is It Biology or Technology That Is the Issue?

Jakob W. Kist, Bart de Keizer, Otto S. Hoekstra and Wouter V. Vogel
Journal of Nuclear Medicine February 2017, 58 (2) 354-355; DOI: https://doi.org/10.2967/jnumed.116.181685
Jakob W. Kist
*Netherlands Cancer Institute Plesmanlaan 121 Amsterdam, 1066CX, Netherlands. E-mail:
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  • For correspondence: j.kist@nki.nl
Bart de Keizer
*Netherlands Cancer Institute Plesmanlaan 121 Amsterdam, 1066CX, Netherlands. E-mail:
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  • For correspondence: j.kist@nki.nl
Otto S. Hoekstra
*Netherlands Cancer Institute Plesmanlaan 121 Amsterdam, 1066CX, Netherlands. E-mail:
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  • For correspondence: j.kist@nki.nl
Wouter V. Vogel
*Netherlands Cancer Institute Plesmanlaan 121 Amsterdam, 1066CX, Netherlands. E-mail:
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REPLY: Thank you for the opportunity to respond to the letter to the editor by Pattison et al. regarding our article presenting the results of the THYROPET study (1). That study showed that after preparation with recombinant human thyroid-stimulating hormone (rh-TSH), 124I PET/CT could not predict the outcome of the posttherapy 131I scan after thyroid hormone withdrawal (THW) in patients with suspected recurrence of differentiated thyroid cancer. We discussed several factors potentially causing these disappointing results; both technical issues regarding 124I PET/CT acquisition and biologic matters were put forward.

Pattison et al. argue that the biologic explanations are most probably causing the false-negative 124I PET/CT scans. We fully agree that the difference in the method of preparation on the 124I PET/CT (after rhTSH injections) and the 131I therapy with posttherapy scanning (after THW) is a likely cause of the 124I PET/CT being false-negative. Data from ours and other studies support this hypothesis (1–3). Confirmation through prospective studies with intrapatient comparisons of rhTSH- and THW-stimulated 124I PET/CT is warranted.

Notably, the one important downside of 124I PET/CT scanning after THW as a diagnostic tool is the reduced quality of life during the period of THW (4).

Whether technical issues can be ruled out as a factor, as argued by Pattison et al., is in our opinion not definite. The sensitivity of 124I PET/CT is shown to be confined by specific scanner characteristics (e.g., no time-of-flight or point-spread function) (5). New scan protocols and new-generation scanners will—to a greater or lesser degree—improve the sensitivity of 124I PET/CT. Similarly, higher administered doses of 124I (e.g., 222 MBq as applied by Ho et al. (6)) might improve lesion detection. Currently, it is not known whether the lesions detected by the improved sensitivity of 124I PET/CT can be treated with a curative administered dose of 131I without exceeding safety limits for bone marrow. Future studies are needed to elucidate this.

In conclusion, we agree with Pattison et al. that the method of preparation on the 124I PET/CT is probably the most important factor causing false-negative 124I PET/CT findings. However, it is too early to state that it is the only factor.

Footnotes

  • Published online Sep. 22, 2016.

  • © 2017 by the Society of Nuclear Medicine and Molecular Imaging.

REFERENCES

  1. 1.↵
    1. Kist JW,
    2. de Keizer B,
    3. van der Vlies M,
    4. 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;57:701–707.
    OpenUrlAbstract/FREE Full Text
  2. 2.
    1. Van Nostrand D,
    2. Khorjekar GR,
    3. O’Neil J,
    4. et al
    . Recombinant human thyroid-stimulating hormone versus thyroid hormone withdrawal in the identification of metastasis in differentiated thyroid cancer with 131I planar whole-body imaging and 124I PET. J Nucl Med. 2012;53:359–362.
    OpenUrlAbstract/FREE Full Text
  3. 3.↵
    1. Freudenberg LS,
    2. Jentzen W,
    3. Petrich T,
    4. et al
    . Lesion dose in differentiated thyroid carcinoma metastases after rhTSH or thyroid hormone withdrawal: 124I PET/CT dosimetric comparisons. Eur J Nucl Med Mol Imaging. 2010;37:2267–2276.
    OpenUrlCrossRefPubMed
  4. 4.↵
    1. Nygaard B,
    2. Bastholt L,
    3. Bennedbæk FN,
    4. Klausen TW,
    5. Bentzen JA
    . Placebo-controlled, blinded and randomised study on the effects of recombinant human thyrotropin on quality of life in the treatment of thyroid cancer. Eur Thyroid J. 2013;2:195–202.
    OpenUrlPubMed
  5. 5.↵
    1. Beijst C,
    2. Kist JW,
    3. Elschot M,
    4. et al
    . Quantitative comparison of 124I PET/CT and 131I SPECT/CT detectability. J Nucl Med. 2016;57:103–108.
    OpenUrlAbstract/FREE Full Text
  6. 6.↵
    1. Ho AL,
    2. Grewal RK,
    3. Leboeuf R,
    4. et al
    . Selumetinib-enhanced radioiodine uptake in advanced thyroid cancer. N Engl J Med. 2013;368:623–632.
    OpenUrlCrossRefPubMed
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Journal of Nuclear Medicine: 58 (2)
Journal of Nuclear Medicine
Vol. 58, Issue 2
February 1, 2017
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Reply: THYROPET Study: Is It Biology or Technology That Is the Issue?
Jakob W. Kist, Bart de Keizer, Otto S. Hoekstra, Wouter V. Vogel
Journal of Nuclear Medicine Feb 2017, 58 (2) 354-355; DOI: 10.2967/jnumed.116.181685

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Reply: THYROPET Study: Is It Biology or Technology That Is the Issue?
Jakob W. Kist, Bart de Keizer, Otto S. Hoekstra, Wouter V. Vogel
Journal of Nuclear Medicine Feb 2017, 58 (2) 354-355; DOI: 10.2967/jnumed.116.181685
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