Management of Patients with Differentiated Thyroid Cancer
Management of Patients with Differentiated Thyroid Cancer
Published: October 2008
Therapy and Prediction of Recurrence in Thyroid Cancer
Consequently, the general survival rate of patients with DTC is very high provided treatment is instituted early. The population of survivors has changed due mainly to an earlier primary treatment, and thus strategies presented in the past based on the majority of patients with advanced disease do not apply anymore. Patients are at different risk of recurrence depending on prognostic factors such as age, sex, size of the tumour, stage and histological type. Considering that one-third of recurrences occur after the first decade, and up to 30-40 years after initial apparently successful therapy, and the recurrence/metastases are most often treatable by 131I, a careful follow-up of these patients is pertinent Much controversy surrounds the matter of surgical treatment (see Table 1), most often, though, performed as total thyroidectomy with or without ablation of the remnant with 131I. A more conservative surgica approach (lobectomy+isthmusectomy) has been advocated by some for DTC patients at low risk and with a good a priori prognosis, in particular in patients with papillary microcarcinoma (<1cm) and small (<4cm) minimally invasive follicular thyroid cancers.
Such conservative therapy may, however, have an implication for the efficiency of the follow-up and should be discussed with the patient.1-3,7-9 Equally controversial is the treatment with levothyroxine (L-thyroxne) after surgery with or without ablation. In the past, when TSH measurements were not sufficiently sensitive to distinguish those with hyperthyroidism from those without, the strategy was to suppress TSH to undetectable levels in order to avoid any growth promotion of remaining cancerous cells. This must, however, be considered an obsolete approach with the development of TSH methods able to discriminate hyperthyroid patients from norma controls, and since it has never been proved that complete suppression of TSH is necessary for a favourable survival in patients with low-risk DTC. On the contrary, data from a National Thyroid Cancer Treatment Co-operative Study in the US did not support the concept that suppressing TSH to undetectable, thyrotoxic ranges was required to prevent disease progression. There is an increasing awareness of possible long-term damaging effects - in terms of cardiac arrythmias, cardiovascular deaths and osteoporosis - if survivors are treated life-long to a mild to moderate hyperthyroidism; this is particularly important in post-menopausal women As a practical matter, the most appropriate L-thyroxine dose is that which reduces the serum TSH to just below the lower limit of the normal range for the assay being used (typically 0.1-0.4 mU/l).6
- Mazzaferi EL, Robbins RJ, Spencer CA, et al., A consensus report of the role of serum thyroglobulin as a monitoring method for low-risk patients with papillary thyroid carcinoma, J Clin Endocrinol Metab, 2003;88:1433–41.
- Schlumberger M, Berg G, Cohen O, et al., Follow-up of low risk patients with differentiated thyroid carcinoma: a European perspective, European J Endocrinol, 2004;150:105–12.
- Pacini F, Schlumberger M, Dralle H, et al., European consensus for the management of patients with differentiated thyroid carcinoma of the follicular epithelium, Eur J Endocrinol, 2006;154:787–803.
- NCCN Clinical Practice Guidelines in Oncology, May 2003. www.nccn.org
- British Thyroid Association guidelines: Guidelines for the management of patients with thyroid carcinoma, www.britishthyroid- association.org
- Mazzaferi EL, Kloos RT, Current approaches to primary therapy for papillary and follicular thyroid cancer, J Clin Endocrinol Metab, 2001;86:1447–63.
- Torlontano M, Attard M, Crocetti U, et al., Follow-up of low risk patients with papillary thyroid cancer: role of neck ultrasonography in detecting lymph node metastases, J Clin Endocrinol Metab, 2004;89:3402–7.
- Pacini F, Capezzone M, Elisei R, et al., Diagnostic 131-iodine whole-body scan may be avoided in thyroid cancer patients who have undetectable stimulated serum Tg levels after initial treatment, J Clin Endocrinol Metab, 2002;87:1499–1501.
- Pacini F, Molinaro E, Castagna MG, et al., Recombinant human thyrotropin-stimulated serum thyroglobulin in combination with neck ultrasonography has the highest sensitivity in monitoring differentiated thyroid carcinoma, J Clin Endocrinol Metab, 2003;88:3668–73.
- NACB guidelines, Laboratory Support for the diagnosis and monitoring of thyroid diseases, Thyroid, 2003;13:1–126. www.nacb.org
- Pacini F, Molinaro E, Lippi F, et al., Prediction of disease status by recombinant human TSH-stimulated serum thyroglobulin in the postsurgical follow-up of differentiated thyroid carcinoma, J Clin Endocrinol Metab, 2001;86:5686–90.
- Robbins RJ, Tuttle RM, Sharaf RN, et al., Preparation by recombinant human thyrotropin or thyroid hormone withdrawal are comparable for the detection of residual differentiated thyroid carcinoma, J Clin Endocrinol Metab, 2001;86:619–25.
- Robbins RJ, Chon JT, Fleischer M, et al., Is the serum thyroglobulin response to recombinant human thyrotropin sufficient, by itself, to monitor for residual thyroid carcinoma?, J Clin Endocrinol Metab, 2002;87:3242–7.
- 11 September 2010






