Volume 6 Supplement 1

European comments on Medullary Thyroid Cancer Management Guidelines of the American Thyroid Association

Open Access

Clinical comments related to medullary thyroid cancer diagnosis and management

Thyroid Research20136(Suppl 1):S6

DOI: 10.1186/1756-6614-6-S1-S6

Published: 14 March 2013

Abstract

Background

The American Thyroid Association (ATA) and more recently the European Thyroid Association (ETA) Guidelines on diagnosis and treatment of medullary thyroid carcinoma (MTC) have provided an excellent tool which was formerly lacking in the field of management of MTC. However, some relevant clinical questions, as the use of somatostatin analogues in the treatment of MTC and the management of pregnant patients with MTC, which were recommended in the guidelines, have been lately extensively revised. Moreover the current issue whether GLP-1 (a glucagon-like peptide-1) analogue is associated with MTC has only superficially been analyzed.

Methods

Publications have been retrieved in MEDLINE at Pubmed (there is no fix date retrospectively) up to October 2012 using the terms “medullary thyroid carcinoma”, “somatostatin”, “pregnancy” and “incretins”. The recommendations made by ATA and ETA were considered.

Conclusions

There are no data supporting the application of somatostatin analogues in the treatment of MTC, while thyroid cancer during or after pregnancy has no impact on the prognosis of disease or on the outcome of pregnancy. However, women with MEN 2 should be carefully controlled before any planned or during any unplanned pregnancy. In contrast to animal studies, there are no consistent human data supporting a stimulatory effect of GLP-1 receptor activation by liraglutide, an incretin mimetic, on calcitonin levels, though establishment of a registry and further studies are required to exclude any association between GLP-1 analogue and MTC.

Background

MTC, which accounts for 5-8% of all thyroid cancers, is mainly sporadic in nature, while a hereditary pattern (multiple endocrine neoplasia type 2 (MEN 2), transmitted as an autosomal-dominant trait due to germline mutations of the RET proto-oncogene, accounts for about 29% of cases [1].

In 2009, at the ETA annual meeting in Lisbon, the European Thyroid Association-Cancer Research Network (ETA-CRN) extensively commented on the American Thyroid Association Guidelines regarding the diagnosis and treatment of medullary thyroid cancer (MTC) published earlier that year [2]. These, in conjunction with the 2011 European Thyroid Association (ETA) Guidelines [3], succeeded in compensating for the previous lack of consensus on the management of this rare disease and now present a platform for optimal diagnostic and therapeutic approach to MTC, one which moreover demands multidisciplinary engagement. Some of the above mentioned comments, updated by references to current publications and expanded by several emerging findings, are highlighted in the present article which seeks to offer a broader perspective concerning certain clinical queries and the recommendations made.

Clinical questions

An oft-posed query: might somatostatin analogues be applicable as antitumor agents in MTC?

MTC is derived from the neural crest and exhibits a widely variable expression of somatostatin receptors which have been used in the detection of disease. Initially octreotide and recently 68Ga DOTA-peptides PET have been successfully employed for the detection of MTC neuroendocrine tumors [4]. More recent developments have provided encouraging results in imaging modalities of MTC, such as PET/CT with beta-emitter labeled DOTANOC, characterized by great affinity to the somatostatin receptors [5]. However, (18)F-DOPA PET/CT seems to be the most valuable imaging method in detecting recurrent MTC [6]. The optimal treatment of MTC is total thyroidectomy and removal of any metastatic tissue from the cervical region. Thus, any alternative treatment should be evaluated on an individual basis.

There are no randomized control studies but only case series or unsystematically conducted studies which were not able to demonstrate any consistent antitumor somatostatin effect. All studies (Table 1), which in total included 55 patients, showed subjective and biological partial remission in one third and in one fourth of the MTC patients, respectively, but no improvement in the natural course of the tumor [7]. Somatostatin analogues, i.e. octreotide or lanreotide, were administered at a dose of 200-1500 micrograms. Despite an initial decrease of calcitonin (Ct) and/of carcinoembryonic antigen (CEA) levels of up to 68% of the basal levels, there was a rebound within a few weeks to 84% and 105%, respectively, of the pretreatment values, thus indicating tachyphylaxis [7, 8]. However, in another study a continuous effect on Ct was observed in two patients with MEN IIa treated with octreotide at a dose 1.5-2 mg/day [9]. More evident was an improvement in clinical symptoms as diarrhea, malaise and weight loss in all the patients [9]. Nevertheless, the results are notably heterogeneous, such as in a study including 18 patients where a greater than 20% decrease of Ct was apparently dependent on the dose of octreotide and the extent of disease (10). In contrast, different formulations of octreotide and lanreotide did not modify Ct and CEA levels in five patients with recurrent MTC treated over a period of 12 weeks [11]. In cases of advanced MTC with ectopic corticotropin-releasing hormone (CRH) and adrenocorticotropic hormone (ACTH) production leading to Cushing syndrome, the use of somatostatin analogues, especially when combined with interferon-alpha, improved diarrhea only transitorily in a few patients [12].
Table 1

Evaluation of somatostatin analogues in advanced medullary thyroid cancer.

Reference

Study

Treatment / Duration

No. of patients

Outcome

Vainas I et al. 2004

OS

Octreotide-(LAR)/ 21 months

22

No improvement of the natural course

Diez IJ, Iglesias P 2002

OS

Octreotide / Lanreotide / 12 weeks

5

No effect

Frank-Raue K et al. 1993

OS

Octreotide

7

No effect No beneficial effect on diarrhea

Mahler C et al. 1990

CR

Octreotide / 17 months

1 2

Tachyphylaxis

Modigliani E et al. 1989

OS

Octreotide / 37 days

18

Improvement of diarrhea in 2/9

OS: observational study, CR: control study

In summary, somatostatin analogues are ineffective in controlling tumor growth and are not recommended by ATA and ETA Guidelines as antitumor agents in MTC.

Basing their assessments on the currently available evidence, both the ATA and ETA Guidelines have recommended against the use of somatostatin analogues in MTC: Grade F (Rec. 84) [2] and Grade 2 and Quality of evidence + [3].

Does medullary thyroid cancer compromise pregnancy?

There are only isolated healthcare reports of management of thyroid cancer (TC) discovered during or after pregnancy and TC does not appear to have a significant impact on the prognosis of the disease. Nor do Ct levels compromise pregnancy. Increase of Ct levels without localization of the disease should not constitute an absolute contraindication of pregnancy. However, in the event that multiple endocrine neoplasia 2A (MEN 2A), which is characterized by MTC, adrenal pheochromocytoma and hyperparathyroidism due to specific RET proto-oncogene mutations, remains unrecognized during pregnancy, then both woman and progeny are at risk of a crisis and of RET mutation transmission, respectively [13].

A case of bilateral pheochromocytoma in a term-pregnant patient with a previous history of MTC was described [14]. The genetic study revealed a heterozygous mutation, c.1900T>C, in the RET proto-oncogene that confirmed the diagnosis of multiple endocrine neoplasia type 2A (MEN2A). Unfortunately, the tumors remained unrecognized and caused a crisis with fatal outcome for the mother during the postpartum period. This instance, though rare, nevertheless underlines the necessity of controlling pregnant patients with a history of MTC, since early detection in such cases is capable of saving the mother and the fetus.

The Guidelines recommend screening for pheochromocytoma in women with RET mutation associated with MEN 2 before a planned pregnancy or at the beginning of an unplanned pregnancy: Grade B (Recommendation 25) [2].

Do glucagon-like peptide-1 analogues increase the incidence of MTC?

Studies in rodents showed that the antidiabetic agent liraglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist, increased risk of thyroid C-cell focal hyperplasia, a state which in rodents is considered as a preneoplastic lesion resulting in MTC, and C-cell tumors [15]. In humans, increases of calcitonin in patients injecting the incretin mimetic liraglutide, albeit falling within the normal range, were observed. Despite the acknowledged limitations to extrapolating findings from animal studies to humans, the results in rodents may possibly indicate a low risk for humans (14). Recently, a study was designed to determine whether GLP-1 receptor activation by liraglutide over a period of two years has an impact on Ct levels in type 2 diabetes mellitus and nondiabetes obese controls [16]. There was no consistent dose or time-dependent relationship between treatment groups, this suggesting that GLP-1 receptor activation has no effect on c-cell activity. However, as has been stated by the FDA, a cancer registry to monitor the annual incidence of MTC over the next 15 years is required in order to clarify any possible association between liraglutide and MTC.

List of abbreviations used

ACTH: 

adrenocorticotropic hormone

CEA: 

carcinoembryonic antigen

CRH: 

corticotropin-releasing hormone

Ct: 

calcitonin

DT: 

doubling time

GLP-1: 

glucagon-like peptide-1

MEN2A: 

multiple endocrine neoplasia type 2A

MTC: 

medullary thyroid carcinoma.

Declarations

Declarations

This article has been published as part of Thyroid Research Volume 6 Supplement 1, 2013: European comments on Medullary Thyroid Cancer Management Guidelines of the American Thyroid Association. The full contents of the supplement are available online at http://www.thyroidresearchjournal.com/supplements/6/S1. Publication of this supplement has been supported by the European Thyroid Association-Cancer Research Network.

Authors’ Affiliations

(1)
Unit of Endocrinology, Diabetes and Metabolism, Evgenidion Hospital, University of Athens Medical School

References

  1. Pacini F, Castagna MG, Cipri C, Schlumberger M: Medullary thyroid carcinoma. Clin Oncol (R Coll Radiol) 2010, 22: 475–85. 10.1016/j.clon.2010.05.002View ArticleGoogle Scholar
  2. Kloos RT, Eng Ch, Evans DB, Francis GL, Gagel RF, Gharib H, Moley JF, Pacini F, Ringel MD, Schlumberger M, Wells SA Jr.: Medullary Thyroid Cancer: Management Guidelines of the American Thyroid Association. Thyroid 2009, 19: 565–612. 10.1089/thy.2008.0403View ArticlePubMedGoogle Scholar
  3. Schlumberger M, Bastholt L, Dralle H, Jarzab B, Pacini F, Smit JWA: 2012 European Thyroid Association Guidelines for Metastatic Medullary Thyroid Cancer. Eur Thyroid J 2012, 1: 5–14. 10.1159/000336977PubMed CentralView ArticlePubMedGoogle Scholar
  4. Nicolini S, Valentina A, Lorenzo F, Stefano F: 68Ga DOTANOC PET/CT detects medullary thyroid cancer relapse at bone level. Clin Nucl Med 2012, 37: 591–2. 10.1097/RLU.0b013e31824c5eabView ArticlePubMedGoogle Scholar
  5. Biermann K, Biersack HJ, Sabet A, Janzen V: Alternative therapeutic approaches in the treatment of primary and secondary dedifferentiated and medullary thyroid carcinoma. Semin Nucl Med 2011, 41: 139–48. 10.1053/j.semnuclmed.2010.10.005View ArticlePubMedGoogle Scholar
  6. Treglia G, Castaldi P, Villani MF, Perotti G, de Waure C, Filice A, et al.: Coparison of 18F-DOPA, 18F-FDG and 68Ga-somatostatin analogue PET/CT in patients with recurrent medullary thyroid carcinoma. Eur J Nucl Med Mol Imaging 2012, 39: 569–580. 10.1007/s00259-011-2031-6View ArticlePubMedGoogle Scholar
  7. Vainas I, Koussis Ch, Pazaitou-Panayiotou K, Drimonitis A, Chrisoulidou A, Iakovou I, Boudina M, Kaprara A, Maladaki A: Somatostatin receptor expression in vivo and response to somatostatin analog therapy with or without other antineoplastic treatments in advanced medullary thyroid carcinoma. J Exp Clin Cancer Res 2004, 23: 549–559.PubMedGoogle Scholar
  8. Frank-Raue K, Ziegler R, Raue F: The use of octreotide in the treatment of medullary thyroid carcinoma. Horm Metab Res Suppl 1993, 27: 44–7.PubMedGoogle Scholar
  9. Mahler C, Verhelst J, de Longueville M, Harris A: Long-term treatment of metastatic medullary thyroid carcinoma with the somatostatin analogue octreotide. Clin Endocrinol (Oxf) 1990, 33: 261–9. 10.1111/j.1365-2265.1990.tb00490.xView ArticleGoogle Scholar
  10. Modigliani E, Guliana JM, Maroni M, Guillausseau JP, Chabrier G, Dupont JL, Caron J, Roger P, Bentata Pessayre M, Jacob C, et al.: Effects of subcutaneous administration of sandostatine (SMS 201.995) in 18 cases of thyroid medullary cancer. Ann Endocrinol (Paris) 1989, 50: 483–8.Google Scholar
  11. Díez JJ, Iglesias P: Somatostatin analogs in the treatment of medullary thyroid carcinoma. J Endocrinol Invest 2002, 25: 773–8.View ArticlePubMedGoogle Scholar
  12. Vitale G, Tagliaferri P, Caraglia M, Rampone E, Ciccarelli A, Bianco AR, Abbruzzese A, Lupoli G: Slow release lanreotide in combination with interferon-alpha2b in the treatment of symptomatic advanced medullary thyroid carcinoma. J Clin Endocrinol Metab 2000, 85: 983–8. 10.1210/jc.85.3.983PubMedGoogle Scholar
  13. Martinelli P, Maruotti GM, Pasquali D, Paladini D, Agangi A, Rippa E, Colantuoni V, Bellastella A, Sinisi AA: Genetic prenatal RET testing and pregnancy management of multiple endocrine neoplasia 2 A (MEN2A): a case report. J Endocrinol Invest 2004, 27: 357–360.View ArticlePubMedGoogle Scholar
  14. Wattanachanya L, Bunworasate U, Plengpanich W, Houngngam N, Buranasupkajorn P, Sunthornyothin S, Shotelersuk V, Snabboon T: Bilateral pheochromocytoma during the postpartum period. Arch Gynecol Obstet 2009, 280: 1055–1058. 10.1007/s00404-009-1057-5View ArticlePubMedGoogle Scholar
  15. Parks M, Rosebraugh C: Weighing Risks and Benefits of Liraglutide — The FDA's Review of a New Antidiabetic Therapy. New Engl J Med 2010, 362: 774–777. 10.1056/NEJMp1001578View ArticlePubMedGoogle Scholar
  16. Hegedüs L, Moses AC, Zdravkovic M, Le Thi T, Daniels GH: GLP-1 and calcitonin concentration in humans: lack of evidence of calcitonin release from sequential screening in over 5000 subjects with type 2 diabetes or nondiabetic obese subjects treated with the human GLP-1 analog, liraglutide. J Clin Endocrinol Metab 2011, 96: 853–860. 10.1210/jc.2010-2318View ArticlePubMedGoogle Scholar

Copyright

© Duntas; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Advertisement