Clinical Oncology
Volume 22, Issue 2 , Pages 136-139, March 2010

Should We Routinely Offer a Second Admission for Radioiodine to Patients with High-risk Differentiated Thyroid Cancer?

  • G.E. Gerrard

      Affiliations

    • Corresponding Author InformationAuthor for correspondence: G.E. Gerrard, St James Institute of Oncology, St James's Hospital, Becket Street, Leeds LS9 7TF, UK. Tel: +44-113-2068336; Fax: +44-113-2067534.
  • ,
  • L. O'Toole
  • ,
  • F. Roberts

St James Institute of Oncology, St James's Hospital, Becket Street, Leeds LS9 7TF, UK

Received 1 October 2009; received in revised form 14 December 2009; accepted 21 December 2009.

Abstract 

Aims

To assess whether an elective second admission for radioiodine is useful for patients with high-risk differentiated thyroid cancer (DTC).

Materials and methods

A retrospective analysis was carried out on 47 high-risk DTC patients treated with a second admission for radioiodine at our centre during the 2007–2008 period.

Results

In 21 patients (45%), the surgeon described an incomplete resection. Twenty-six (55%) had surgical macroscopic complete resection, but cancer cells at the margin of excision histologically. Overall, at the second admission for radioiodine, 27 patients (57%) had a normal post-treatment scan and undetectable thyroid-stimulating hormone (TSH) stimulated thyroglobulin. Twenty patients (43%) had raised stimulated thyroglobulin at second admission for radioiodine, of whom only six (13%) had abnormal uptake (>0.1%) on the post-treatment scan.

Conclusions

A second admission for radioiodine could have been avoided in most patients. Instead, information from stimulated thyroglobulin and a diagnostic radioiodine scan would have been sufficient to guide further management. This study also provides interesting outcome data on incompletely resected DTC.

Key words: High-risk DTC, postoperative residual cancer, radioiodine, radiotherapy, raised thyroglobulin, thyroid cancer

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PII: S0936-6555(10)00005-1

doi:10.1016/j.clon.2010.01.002

Clinical Oncology
Volume 22, Issue 2 , Pages 136-139, March 2010