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DOI 10.1210/jc.2016-3640

Медицинская библиотека · The Journal of clinical endocrinology and metabolism · 2017

Risk Profile of the RET A883F Germline Mutation: An International Collaborative Study.

Mathiesen Jes Sloth, Habra Mouhammed Amir, Bassett John Howard Duncan, Choudhury Sirazum Mubin, Balasubramanian Sabapathy Prakash, Howlett Trevor A, Robinson Bruce G, Gimenez-Roqueplo Anne-Paule, Castinetti Frederic, Vestergaard Peter, Frank-Raue Karin

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Аннотация

CONTEXT: The A883F germline mutation of the rearranged during transfection (RET) proto-oncogene causes multiple endocrine neoplasia 2B. In the revised American Thyroid Association (ATA) guidelines for the management of medullary thyroid carcinoma (MTC), the A883F mutation has been reclassified from the highest to the high-risk level, although no well-defined risk profile for this mutation exists.

OBJECTIVE

To create a risk profile for the A883F mutation for appropriate classification among the ATA risk levels.

DESIGN

Retrospective analysis.

SETTING

International collaboration.

PATIENTS: Included were 13 A883F carriers.

INTERVENTION: The intervention was thyroidectomy.

MAIN OUTCOME MEASURES: Earliest age of MTC, regional lymph node metastases, distant metastases, age-related penetrance of MTC and pheochromocytoma (PHEO), overall and disease-specific survival, and biochemical cure rate.

RESULTS

One and three carriers were diagnosed at age 7 to 9 years (median, 7.5 years) with a normal thyroid and C-cell hyperplasia, respectively. Nine carriers were diagnosed with MTC at age 10 to 39 years (median, 19 years). The earliest age of MTC, regional lymph node metastasis, and distant metastasis was 10, 20, and 20 years, respectively. Fifty percent penetrance of MTC and PHEO was achieved by age 19 and 34 years, respectively. Five- and 10-year survival rates (both overall and disease specific) were 88% and 88%, respectively. Biochemical cure for MTC at latest follow-up was achieved in 63% (five of eight carriers) with pertinent data.

CONCLUSIONS

MTC of A883F carriers seems to have a more indolent natural course compared with that of M918T carriers. Our results support the classification of the A883F mutation in the ATA high-risk level.

Для цитирования: Mathiesen Jes Sloth, Habra Mouhammed Amir, Bassett John Howard Duncan, Choudhury Sirazum Mubin, Balasubramanian Sabapathy Prakash, Howlett Trevor A, Robinson Bruce G, Gimenez-Roqueplo Anne-Paule, Castinetti Frederic, Vestergaard Peter, Frank-Raue Karin. Risk Profile of the RET A883F Germline Mutation: An International Collaborative Study.. The Journal of clinical endocrinology and metabolism. 2017. DOI: 10.1210/jc.2016-3640.

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