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First published online January 21, 2009, 10.2967/jnumed.108.057349
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Journal of Nuclear Medicine Vol. 50 No. 2 329-330
© 2009 by Society of Nuclear Medicine

doi: 10.2967/jnumed.108.057349

Reply: A Proposition for the Use of Radioiodine in WDTC Management

Ian D. Hay

Mayo Clinic
Rochester, Minnesota

I. Ross McDougall

Stanford University Hospital and Clinics
Stanford, California

James C. Sisson

University of Michigan Health System
Ann Arbor, Michigan

REPLY: We appreciate Professor Bourgeois' thoughtful letter. Our perspective (1) was limited to making major points to indict ablation in the management of thyroid carcinomas, and Professor Bourgeois' questions offer an opportunity to expand on our thesis.

We agree with Professor Bourgeois that refinements in scintigraphic imaging will more accurately define the anatomic sites of residual functioning thyroid tissues. The sensitivity of imaging is also likely to improve over time. We further agree that diagnostic scintigraphic imaging may help to locate residual carcinomas and thereby aid in decisions about therapy (surgical or 131I). Although images made after ablation therapy may be more sensitive than pretherapeutic scans, we do not believe that this observation justifies such management of patients who have stage I carcinomas. If, from data available, there is concern about carcinoma not seen on the diagnostic images, consideration may be given to treatment, not ablation, with 131I. However, long-term benefits from this approach have not been shown. We also agree that if 131I treatments are to be given for carcinomas, the administered dose should be optimal, a goal that often requires dosimetry.

Whereas thyroglobulin antibodies often disappear over time after 131I ablation (2), it is possible that this immune interference may also disappear without radiation treatment. In any case, such antibodies may serve as a surrogate for circulating tumor thyroglobulin (3).

Because papillary microcarcinomas are so frequently present, the numbers of patients are difficult to grasp. From autopsy evidence, such tumors have been found in 1.4%–36% of populations around the world (46). In addition, of those afflicted, multifocality was found in 20%–47% and micrometastases to cervical lymph nodes in 3%–18% (4), yet cause-specific mortality was 0%–1% (6). Nevertheless, after surgical therapy, recurrences have been documented. For patients with primary tumors smaller than 5 mm, recurrences appear in about 1% (7). In follow-up, cervical metastases were discovered more frequently if, at the time of the original operation, the lymph nodes contained carcinoma (8,9). Hay et al. found that postoperative 131I treatments were not followed by statistically fewer nodal recurrences (8), but Chow et al. reported that, after ablation, new cervical disease was statistically less common (9). However, overall, recurrences in the absence of ablation therapy were seen in few patients: only 11 (8) and 4 (9).

Some patients with microcarcinomas may require therapy after surgical removal of the tumors; depending on ancillary findings, treatments will vary (6,10). Still, it is important to remember that the prognosis for most patients with microcarcinomas is excellent. Because of the frequency of this tumor in the population, accepted treatments will have wide applications, and those with unsubstantiated efficacy, including the radiation from ablation, are likely to do much more harm than good.

Therapies for the uncommon variants of papillary carcinoma, such as tall cell or insular, have not been thoroughly studied, but it is difficult to see how ablation would be helpful for patients with these neoplasms. Follicular carcinomas have recently been classified as minimally invasive (capsule only), moderately invasive (angioinvasion), and widely invasive (11), distinctions that appear to be helpful in addition to the prognostic schemes of MACIS (metastases, age, completeness of resection, invasion, size) and TNM (12).

Recently, an editorial created by many contributors discussed and promoted recombinant human thyroid-stimulating hormone for ablation (13). Recombinant thyroid-stimulating hormone has not been approved by the Food and Drug Administration for treatment with 131I. In the past, 131I ablations and 131I treatments of thyroid carcinoma have sometimes been used interchangeably, but the differences must now be addressed. Except when a large amount of residual thyroid tissue inhibits TSH secretion after an incomplete surgical thyroidectomy, ablation has no role. Thyroidectomies should be performed by well-trained surgeons; incomplete thyroidectomies should then be uncommon. We believe that research should focus on how better to treat health-impairing and life-threatening carcinomas for which 131I is an important therapy.

FOOTNOTES

COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.

References

  1. Hay ID, McDougall IR, Sisson JC. Perspective: the case against radioiodine remnant ablation in patients with well-differentiated thyroid carcinoma. J Nucl Med. 2008;49:1395–1397.[Abstract/Free Full Text]
  2. Chiovato L, Latrofa F, Braverman LE, et al. Disappearance of humoral thyroid autoimmunity after complete removal of thyroid antigens. Ann Intern Med. 2003;139:346–351.[Abstract/Free Full Text]
  3. Spencer CA, Bergoglio LM, Kazarosyan M, Fatemi S, LoPresti JS. Clinical impact of thyroglobulin (Tg) and Tg autoantibody method differences on the management of patients with differentiated thyroid carcinomas. J Clin Endocrinol Metab. 2005;90:5566–5575.[Abstract/Free Full Text]
  4. Bramley MD, Harrison BJ. Papillary microcarcinoma of the thyroid gland. Br J Surg. 1996;83:1674–1683.[CrossRef][Medline]
  5. Kovacs GL, Gonda G, Vadasz G, et al. Epidemiology of thyroid microcarcinoma found in autopsy series conducted in areas of different iodine intake. Thyroid. 2005;15:152–157.[CrossRef][Medline]
  6. Pazaitou-Panayiotou K, Capezzone M, Pacini F. Clinical features and therapeutic implication of papillary thyroid microcarcinoma. Thyroid. 2007;17:1085–1092.[CrossRef][Medline]
  7. Roti E, Rossi R, Trasforini G, et al. Clinical and histologic characteristics of papillary thyroid microcarcinoma: results of a retrospective study of 243 patients. J Clin Endocrinol Metab. 2006;91:2171–2178.[Abstract/Free Full Text]
  8. Hay ID, Grant CS, van Heerden JA, Goellner JR, Ebersold JR. Bergstralh EJ. Papillary thyroid microcarcinoma: a study of 535 cases observed in a 50-year period. Surgery. 1992;112:1139–1146.[Medline]
  9. Chow S-M, Law SKW, Chan JKC, Au S-K, Yau S, Lau W-H. Papillary microcarcinoma of the thyroid: prognostic significance of lymph node metastases and multifocality. Cancer. 2003;98:31–40.[CrossRef][Medline]
  10. McDougall IR, Carnargo CA. Treatment of micropapillary carcinoma of the thyroid: where do we draw the line? Thyroid. 2007;17:1093–1096.[CrossRef][Medline]
  11. D'Avanzo A, Treseler P, Ituarte PHG, et al. Follicular carcinoma: histology and prognosis. Cancer. 2004;100:1123–1129.[CrossRef][Medline]
  12. D'Avanzo A, Ituarte P, Treseler P, et al. Prognostic scoring systems in patients with follicular thyroid cancer: a comparison of different staging systems in predicting the patient outcome. Thyroid. 2004;14:453–458.[CrossRef][Medline]
  13. Haugen BR, Emerson C, Pacini F, et al. Expanding indications for recombinant human TSH in thyroid cancer. Thyroid. 2008;18:687–694.[CrossRef][Medline]




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