Is new American Thyroid Association risk classification for hereditary medullary thyroid carcinoma applicable to Chinese patients? A single-center study

被引:5
作者
Zhang, Xiwei [1 ,2 ]
Yan, Dangui [1 ,2 ]
Wang, Junyi [3 ]
Wan, Hanfeng [4 ]
Zhang, Yongxia [5 ]
Zhang, Yabing [1 ,2 ]
He, Yuqin [1 ,2 ]
Liu, Wensheng [1 ,2 ]
Zhang, Bin [6 ]
机构
[1] Chinese Acad Med Sci, Canc Hosp, Natl Canc Ctr, Dept Head & Neck Surg Oncol, Beijing 100021, Peoples R China
[2] Peking Union Med Coll, Beijing 100021, Peoples R China
[3] Tianjin Med Univ, Dept Thyroid & Neck Tumor, Key Lab Canc Prevent & Therapy Tianjin, Canc Inst & Hosp,Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[4] Shanghai Jiao Tong Univ, Renji Hosp, Dept Otorhinolaryngol Head & Neck Surg, Sch Med, Shanghai 200127, Peoples R China
[5] Chinese Peoples Liberat Army PLA Gen Hosp, Dept Otorhinolaryngol Head & Neck Surg, Beijing 100853, Peoples R China
[6] Peking Univ, Canc Hosp & Inst, Minist Educ Beijing, Dept Head & Neck Surg Oncol,Key Lab Carcinogenesi, Beijing 100142, Peoples R China
关键词
Medullary thyroid carcinoma (MTC); rearranged during transfection (RET); genotype-phenotype correlation; multiple endocrine neoplasia type 2 (MEN2); prophylactic thyroidectomy; ENDOCRINE NEOPLASIA TYPE-2; RET PROTOONCOGENE; MUTATIONS; PHENOTYPE; GENE; GUIDELINES; SURGERY; DOMAIN; 2B;
D O I
10.21147/j.issn.1000-9604.2017.03.08
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The American Thyroid Association (ATA) proposed a new risk classification for hereditary medullary thyroid carcinoma (MTC) in 2015. This study aimed to assess whether the new guidelines are suitable for the Chinese population, and reported our experience on prophylactic thyroidectomy. Methods: A total of 73 patients from 22 families were screened as rearranged during transfection (RET) mutation carriers from 2010 to 2016 in Cancer Hospital, Chinese Academy of Medical Science; the medical history for each patient was collected. Based on the initial treatment, we identified the risk factors for poor prognosis by univariate and multivariate logistic regression. Then, 4 RET mutation carriers were enrolled for prophylactic thyroidectomy, and their pathological data and follow-up outcomes were recorded. Results: In univariate and multivariate logistic regression analyses, age at initial surgery and risk classification were significant risk factors for stage III/IV hereditary MTC at initial diagnosis. The likelihood was increased by 11.6% per year of age at initial surgery [95% confidence interval (95% CI), 1.040-1.198; P=0.002). It was 7.888 times more likely to have III/IV stage disease for ATA highest risk patients, compared to ATA moderate risk individuals (95% CI, 1.607-38.717; P=0.003). Postoperative pathological results showed all 4 multiple endocrine neoplasia type 2A (MEN2A) patients had C-cell hyperplasia (CCH); multifocal malignancies were detected in 3 of them. All 4 patients were cured biochemically, and none developed permanent hypoparathyroidism. Conclusions: In Chinese individuals, hereditary MTC aggressiveness is in line with the new ATA risk classification. Germline RET gene mutation carriers should undergo prophylactic thyroidectomy according to basal serum calcitonin levels.
引用
收藏
页码:223 / 230
页数:8
相关论文
共 24 条
  • [1] Surgical Curability of Medullary Thyroid Cancer in Multiple Endocrine Neoplasia 2B A Changing Perspective
    Brauckhoff, Michael
    Machens, Andreas
    Lorenz, Kerstin
    Bjoro, Trine
    Varhaug, Jan Erik
    Dralle, Henning
    [J]. ANNALS OF SURGERY, 2014, 259 (04) : 800 - 806
  • [2] SINGLE MISSENSE MUTATION IN THE TYROSINE KINASE CATALYTIC DOMAIN OF THE RET PROTOONCOGENE IS ASSOCIATED WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B
    CARLSON, KM
    DOU, SS
    CHI, D
    SCAVARDA, N
    TOSHIMA, K
    JACKSON, CE
    WELLS, SA
    GOODFELLOW, PJ
    DONISKELLER, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) : 1579 - 1583
  • [3] RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors
    de Groot, Jan Willem B.
    Links, Thera P.
    Plukker, John T. M.
    Lips, Cornelis J. M.
    Hofstra, Robert M. W.
    [J]. ENDOCRINE REVIEWS, 2006, 27 (05) : 535 - 560
  • [4] MUTATIONS IN THE RET PROTOONCOGENE ARE ASSOCIATED WITH MEN 2A AND FMTC
    DONISKELLER, H
    DOU, SS
    CHI, D
    CARLSON, KM
    TOSHIMA, K
    LAIRMORE, TC
    HOWE, JR
    MOLEY, JF
    GOODFELLOW, P
    WELLS, SA
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (07) : 851 - 856
  • [5] Calcitonin estimation in patients with nodular goiter and its significance for early detection of MTC: European comments to the guidelines of the American Thyroid Association
    Elisei R.
    Romei C.
    [J]. Thyroid Research, 6 (Suppl 1)
  • [6] POINT MUTATION WITHIN THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B AND RELATED SPORADIC TUMORS
    ENG, C
    SMITH, DP
    MULLIGAN, LM
    NAGAI, MA
    HEALEY, CS
    PONDER, MA
    GARDNER, E
    SCHEUMANN, GFW
    JACKSON, CE
    TUNNACLIFFE, A
    PONDER, BAJ
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (02) : 237 - 241
  • [7] The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2 - International RET mutation consortium analysis
    Eng, C
    Clayton, D
    Schuffenecker, I
    Lenoir, G
    Cote, G
    Gagel, RF
    vanAmstel, HKP
    Lips, CJM
    Nishisho, I
    Takai, SI
    Marsh, DJ
    Robinson, BG
    FrankRaue, K
    Raue, F
    Xue, FY
    Noll, WW
    Romei, C
    Pacini, F
    Fink, M
    Niederle, B
    Zedenius, J
    Nordenskjold, M
    Komminoth, P
    Hendy, GN
    Gharib, H
    Thibodeau, SN
    Lacroix, A
    Frilling, A
    Ponder, BAJ
    Mulligan, LM
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (19): : 1575 - 1579
  • [8] Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy:: impact of individual RET genotype
    Frank-Raue, K.
    Buhr, H.
    Dralle, H.
    Klar, E.
    Senninger, N.
    Weber, T.
    Rondot, S.
    Hoeppner, W.
    Raue, F.
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2006, 155 (02) : 229 - 236
  • [9] A MUTATION IN THE RET PROTOONCOGENE ASSOCIATED WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-2B AND SPORADIC MEDULLARY-THYROID CARCINOMA
    HOFSTRA, RMW
    LANDSVATER, RM
    CECCHERINI, I
    STULP, RP
    STELWAGEN, T
    LUO, Y
    PASINI, B
    HOPPENER, JWM
    VANAMSTEL, HKP
    ROMEO, G
    LIPS, CJM
    BUYS, CHCM
    [J]. NATURE, 1994, 367 (6461) : 375 - 376
  • [10] Multiple Endocrine Neoplasia Type 2B with a RET Proto-Oncogene A883F Mutation Displays a More Indolent Form of Medullary Thyroid Carcinoma Compared with a RET M918T Mutation
    Jasim, Sina
    Ying, Anita K.
    Waguespack, Steven G.
    Rich, Thereasa A.
    Grubbs, Elizabeth G.
    Jimenez, Camilo
    Hu, Mimi I.
    Cote, Gilbert
    Habra, Mouhammed Amir
    [J]. THYROID, 2011, 21 (02) : 189 - 192