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Published in: World Journal of Surgery 4/2010

Open Access 01-04-2010

Factors Predicting Outcome of Total Thyroidectomy in Young Patients with Multiple Endocrine Neoplasia Type 2: A Nationwide Long-Term Follow-up Study

Authors: Jennifer M. J. Schreinemakers, Menno R. Vriens, Gerlof D. Valk, Jan-Willem B. de Groot, John T. Plukker, Klaas (N.) M. A. Bax, Jaap F. Hamming, Rob B. van der Luijt, Daniel C. Aronson, Inne H. M. Borel Rinkes

Published in: World Journal of Surgery | Issue 4/2010

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Abstract

Background

Multiple endocrine neoplasia type 2 (MEN 2) is caused by a RET mutation in chromosome 10. All MEN 2 patients develop medullary thyroid carcinoma (MTC). The age-related risk of MTC is associated with the type of RET mutation. Our aim was to identify prognostic factors associated with recurrent MTC in MEN 2 patients.

Methods

In a nationwide case–control study, all patients who underwent total thyroidectomy in the Netherlands under the age of 20 years were classified into standard (1), high (2), or very high risk (3) for MTC based on RET-mutation type. Disease-free patients were compared with those with recurrent disease.

Results

A total of 93 patients were included in the study. Sixty-six percent had MTC on histology, the youngest being 1 year old. Codon 634 was most affected. Sixteen (18%) patients had persistent or recurrent disease, one of whom died. Significantly associated determinants of outcome in univariate analysis were higher age at surgery, no age-appropriate prophylactic surgery according to risk level, elevated preoperative calcitonin levels, affected codon, and the presence of lymph node metastases at surgery. On multivariate analysis only age of surgery was the single independent factor associated with persistent disease.

Conclusions

Prophylactic thyroidectomy beyond the recommended age is associated with persistent/recurrent disease. In addition, codon 634 mutation is associated with a high risk of recurrence requiring early surgery for all these patients.
Literature
1.
go back to reference Kraimps JL, Duh QY, Demeure M et al (1992) Hyperparathyroidism in multiple endocrine neoplasia syndrome. Surgery 112(6):1080–1086 (discussion 1086–1088)PubMed Kraimps JL, Duh QY, Demeure M et al (1992) Hyperparathyroidism in multiple endocrine neoplasia syndrome. Surgery 112(6):1080–1086 (discussion 1086–1088)PubMed
2.
go back to reference Raue F, Frank-Raue K, Grauer A (1994) Multiple endocrine neoplasia type 2 Clinical features and screening. Endocrinol Metab Clin North Am 23(1):137–156PubMed Raue F, Frank-Raue K, Grauer A (1994) Multiple endocrine neoplasia type 2 Clinical features and screening. Endocrinol Metab Clin North Am 23(1):137–156PubMed
3.
go back to reference Machens A, Holzhausen HJ, Thanh PN et al (2003) Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations. Surgery 134(3):425–431CrossRefPubMed Machens A, Holzhausen HJ, Thanh PN et al (2003) Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations. Surgery 134(3):425–431CrossRefPubMed
4.
go back to reference Machens A, Ukkat J, Brauckhoff M et al (2005) Advances in the management of hereditary medullary thyroid cancer. J Intern Med 257(1):50–59CrossRefPubMed Machens A, Ukkat J, Brauckhoff M et al (2005) Advances in the management of hereditary medullary thyroid cancer. J Intern Med 257(1):50–59CrossRefPubMed
5.
go back to reference Wolfe HJ, Melvin KE, Cervi-Skinner SJ et al (1973) C-cell hyperplasia preceding medullary thyroid carcinoma. N Engl J Med 289(9):437–441PubMedCrossRef Wolfe HJ, Melvin KE, Cervi-Skinner SJ et al (1973) C-cell hyperplasia preceding medullary thyroid carcinoma. N Engl J Med 289(9):437–441PubMedCrossRef
6.
go back to reference Donis-Keller H, Dou S, Chi D et al (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2(7):851–856CrossRefPubMed Donis-Keller H, Dou S, Chi D et al (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2(7):851–856CrossRefPubMed
7.
go back to reference Lips CJ, Landsvater RM, Hoppener JW et al (1994) Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A. N Engl J Med 331(13):828–835CrossRefPubMed Lips CJ, Landsvater RM, Hoppener JW et al (1994) Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A. N Engl J Med 331(13):828–835CrossRefPubMed
8.
go back to reference Mulligan LM, Kwok JB, Healey CS et al (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363(6428):458–460CrossRefPubMed Mulligan LM, Kwok JB, Healey CS et al (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363(6428):458–460CrossRefPubMed
9.
go back to reference Machens A, Niccoli-Sire P, Hoegel J et al (2003) Early malignant progression of hereditary medullary thyroid cancer. N Engl J Med 349(16):1517–1525CrossRefPubMed Machens A, Niccoli-Sire P, Hoegel J et al (2003) Early malignant progression of hereditary medullary thyroid cancer. N Engl J Med 349(16):1517–1525CrossRefPubMed
10.
go back to reference Skinner MA, Moley JA, Dilley WG et al (2005) Prophylactic thyroidectomy in multiple endocrine neoplasia type 2A. N Engl J Med 353(11):1105–1113CrossRefPubMed Skinner MA, Moley JA, Dilley WG et al (2005) Prophylactic thyroidectomy in multiple endocrine neoplasia type 2A. N Engl J Med 353(11):1105–1113CrossRefPubMed
11.
go back to reference Brandi ML, Gagel RF, Angeli A et al (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 86(12):5658–5671CrossRefPubMed Brandi ML, Gagel RF, Angeli A et al (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 86(12):5658–5671CrossRefPubMed
12.
go back to reference de Groot JW, Links TP, Rouwe CW et al (2006) Prophylactic thyroidectomy in children who are carriers of a multiple endocrine neoplasia type 2 mutation: description of 20 cases and recommendations based on the literature. Ned Tijdschr Geneeskd 150(6):311–318PubMed de Groot JW, Links TP, Rouwe CW et al (2006) Prophylactic thyroidectomy in children who are carriers of a multiple endocrine neoplasia type 2 mutation: description of 20 cases and recommendations based on the literature. Ned Tijdschr Geneeskd 150(6):311–318PubMed
13.
go back to reference Gagel RF, Tashjian AH Jr, Cummings T et al (1988) The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience. N Engl J Med 318(8):478–484PubMed Gagel RF, Tashjian AH Jr, Cummings T et al (1988) The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience. N Engl J Med 318(8):478–484PubMed
14.
go back to reference Orlandi F, Caraci P, Mussa A et al (2001) Treatment of medullary thyroid carcinoma: an update. Endocr Relat Cancer 8(2):135–147CrossRefPubMed Orlandi F, Caraci P, Mussa A et al (2001) Treatment of medullary thyroid carcinoma: an update. Endocr Relat Cancer 8(2):135–147CrossRefPubMed
15.
go back to reference Machens A, Dralle H (2007) Genotype–phenotype based surgical concept of hereditary medullary thyroid carcinoma. World J Surg 31(5):957–968CrossRefPubMed Machens A, Dralle H (2007) Genotype–phenotype based surgical concept of hereditary medullary thyroid carcinoma. World J Surg 31(5):957–968CrossRefPubMed
16.
go back to reference Dralle H, Gimm O, Simon D et al (1998) Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience. World J Surg 22(7):744–750 (discussion 750–741)CrossRefPubMed Dralle H, Gimm O, Simon D et al (1998) Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience. World J Surg 22(7):744–750 (discussion 750–741)CrossRefPubMed
17.
go back to reference Gill JR, Reyes-Mugica M, Iyengar S et al (1996) Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: implications for therapy. J Pediatr 129(3):459–464CrossRefPubMed Gill JR, Reyes-Mugica M, Iyengar S et al (1996) Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: implications for therapy. J Pediatr 129(3):459–464CrossRefPubMed
18.
go back to reference Samaan NA, Draznin MB, Halpin RE et al (1991) Multiple endocrine syndrome type IIb in early childhood. Cancer 68(8):1832–1834CrossRefPubMed Samaan NA, Draznin MB, Halpin RE et al (1991) Multiple endocrine syndrome type IIb in early childhood. Cancer 68(8):1832–1834CrossRefPubMed
19.
go back to reference Skinner MA, DeBenedetti MK, Moley JF et al (1996) Medullary thyroid carcinoma in children with multiple endocrine neoplasia types 2A and 2B. J Pediatr Surg 31(1):177–181 (discussion 181–172)CrossRefPubMed Skinner MA, DeBenedetti MK, Moley JF et al (1996) Medullary thyroid carcinoma in children with multiple endocrine neoplasia types 2A and 2B. J Pediatr Surg 31(1):177–181 (discussion 181–172)CrossRefPubMed
20.
go back to reference Stjernholm MR, Freudenbourg JC, Mooney HS et al (1980) Medullary carcinoma of the thyroid before age 2 years. J Clin Endocrinol Metab 51(2):252–253CrossRefPubMed Stjernholm MR, Freudenbourg JC, Mooney HS et al (1980) Medullary carcinoma of the thyroid before age 2 years. J Clin Endocrinol Metab 51(2):252–253CrossRefPubMed
21.
go back to reference Siggelkow H, Melzer A, Nolte W et al (2001) Presentation of a kindred with familial medullary thyroid carcinoma and Cys611Phe mutation of the RET proto-oncogene demonstrating low grade malignancy. Eur J Endocrinol 144(5):467–473CrossRefPubMed Siggelkow H, Melzer A, Nolte W et al (2001) Presentation of a kindred with familial medullary thyroid carcinoma and Cys611Phe mutation of the RET proto-oncogene demonstrating low grade malignancy. Eur J Endocrinol 144(5):467–473CrossRefPubMed
22.
go back to reference Lindskog S, Nilsson O, Jansson S et al (2004) Phenotypic expression of a family with multiple endocrine neoplasia type 2A due to a RET mutation at codon 618. Br J Surg 91(6):713–718CrossRefPubMed Lindskog S, Nilsson O, Jansson S et al (2004) Phenotypic expression of a family with multiple endocrine neoplasia type 2A due to a RET mutation at codon 618. Br J Surg 91(6):713–718CrossRefPubMed
23.
go back to reference Neocleous V, Passalaris T, Spanou E et al (2004) Description of the first two seemingly unrelated Greek Cypriot families with a common C618R RET proto-oncogene mutation. Genet Test 8(2):163–168CrossRefPubMed Neocleous V, Passalaris T, Spanou E et al (2004) Description of the first two seemingly unrelated Greek Cypriot families with a common C618R RET proto-oncogene mutation. Genet Test 8(2):163–168CrossRefPubMed
24.
go back to reference Frohnauer MK, Decker RA (2000) Update on the MEN 2A c804 RET mutation: is prophylactic thyroidectomy indicated? Surgery 128(6):1052–1057 (discussion 1057–1058)CrossRefPubMed Frohnauer MK, Decker RA (2000) Update on the MEN 2A c804 RET mutation: is prophylactic thyroidectomy indicated? Surgery 128(6):1052–1057 (discussion 1057–1058)CrossRefPubMed
Metadata
Title
Factors Predicting Outcome of Total Thyroidectomy in Young Patients with Multiple Endocrine Neoplasia Type 2: A Nationwide Long-Term Follow-up Study
Authors
Jennifer M. J. Schreinemakers
Menno R. Vriens
Gerlof D. Valk
Jan-Willem B. de Groot
John T. Plukker
Klaas (N.) M. A. Bax
Jaap F. Hamming
Rob B. van der Luijt
Daniel C. Aronson
Inne H. M. Borel Rinkes
Publication date
01-04-2010
Publisher
Springer-Verlag
Published in
World Journal of Surgery / Issue 4/2010
Print ISSN: 0364-2313
Electronic ISSN: 1432-2323
DOI
https://doi.org/10.1007/s00268-009-0370-2

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