Skip to main content
Erschienen in: World Journal of Surgery 1/2018

14.08.2017 | Original Scientific Report

Relationship Between 18F-fluorodeoxyglucose Accumulation and the BRAF V600E Mutation in Papillary Thyroid Cancer

verfasst von: Jae Won Chang, Ki Wan Park, Jae Hyung Heo, Seung-Nam Jung, Lihua Liu, Sung Min Kim, In Sun Kwon, Bon Seok Koo

Erschienen in: World Journal of Surgery | Ausgabe 1/2018

Einloggen, um Zugang zu erhalten

Abstract

Background

To determine whether 18F-fluoro-2-deoxyglucose (18F-FDG)-PET/CT is useful for predicting the BRAF V600E mutation status of a primary papillary thyroid carcinoma (PTC).

Methods

A retrospective analysis was performed in 108 patients who underwent 18F-FDG positron emission tomography–computed tomography (PET/CT) for staging before thyroidectomy and BRAF analysis in biopsy-confirmed PTC. The maximum standardized uptake value (SUVmax) of the primary tumor was calculated according to FDG accumulation. Univariate and multivariate analyses were performed to assess the association between the SUVmax and clinicopathological variables.

Results

The BRAF V600E mutation was detected in 71 of 108 (65.7%) patients. In all subjects, the tumor size and BRAF V600E mutation were independently related to the SUVmax according to multivariate analyses (P = 0.002 and 0.007, respectively). The SUVmax was significantly higher in tumors with the BRAF V600E mutation than in tumors with wild-type BRAF (10.24 ± 11.89 versus 4.02 ± 3.86; P = 0.007). In the tumor size >1 cm subgroup, the BRAF V600E mutation was the only factor significantly associated with the SUVmax (P = 0.016). A SUVmax cutoff level of 4.9 was determined to be significant for predicting the BRAF V600E mutation status (sensitivity 77.4%, specificity 100.0%, area under the curve 0.929; P < 0.0001) according to ROC curve analysis.

Conclusions

The BRAF V600E mutation is independently associated with high 18F-FDG uptake in PTC, especially in those with a tumor size >1 cm.
Literatur
1.
Zurück zum Zitat Lee JW, Lee SM, Lee DH et al (2013) Clinical utility of 18F-FDG PET/CT concurrent with 131I therapy in intermediate-to-high-risk patients with differentiated thyroid cancer: dual-center experience with 286 patients. J Nucl Med 54:1230–1236CrossRefPubMed Lee JW, Lee SM, Lee DH et al (2013) Clinical utility of 18F-FDG PET/CT concurrent with 131I therapy in intermediate-to-high-risk patients with differentiated thyroid cancer: dual-center experience with 286 patients. J Nucl Med 54:1230–1236CrossRefPubMed
2.
Zurück zum Zitat Rosenbaum-Krumme SJ, Gorges R, Bockisch A et al (2012) (1)(8)F-FDG PET/CT changes therapy management in high-risk DTC after first radioiodine therapy. Eur J Nucl Med Mol Imaging 39:1373–1380CrossRefPubMed Rosenbaum-Krumme SJ, Gorges R, Bockisch A et al (2012) (1)(8)F-FDG PET/CT changes therapy management in high-risk DTC after first radioiodine therapy. Eur J Nucl Med Mol Imaging 39:1373–1380CrossRefPubMed
3.
Zurück zum Zitat Robbins RJ, Wan Q, Grewal RK et al (2006) Real-time prognosis for metastatic thyroid carcinoma based on 2-[18F]fluoro-2-deoxy-d-glucose-positron emission tomography scanning. J Clin Endocrinol Metab 91:498–505CrossRefPubMed Robbins RJ, Wan Q, Grewal RK et al (2006) Real-time prognosis for metastatic thyroid carcinoma based on 2-[18F]fluoro-2-deoxy-d-glucose-positron emission tomography scanning. J Clin Endocrinol Metab 91:498–505CrossRefPubMed
4.
Zurück zum Zitat Wang W, Larson SM, Fazzari M et al (2000) Prognostic value of [18F]fluorodeoxyglucose positron emission tomographic scanning in patients with thyroid cancer. J Clin Endocrinol Metab 85:1107–1113PubMed Wang W, Larson SM, Fazzari M et al (2000) Prognostic value of [18F]fluorodeoxyglucose positron emission tomographic scanning in patients with thyroid cancer. J Clin Endocrinol Metab 85:1107–1113PubMed
5.
Zurück zum Zitat Bertagna F, Treglia G, Piccardo A et al (2012) Diagnostic and clinical significance of F-18-FDG-PET/CT thyroid incidentalomas. J Clin Endocrinol Metab 97:3866–3875CrossRefPubMed Bertagna F, Treglia G, Piccardo A et al (2012) Diagnostic and clinical significance of F-18-FDG-PET/CT thyroid incidentalomas. J Clin Endocrinol Metab 97:3866–3875CrossRefPubMed
6.
Zurück zum Zitat Koh J, Choi JR, Han KH et al (2013) Proper indication of BRAF V600E mutation testing in fine-needle aspirates of thyroid nodules. PLoS ONE 8:e64505CrossRefPubMedPubMedCentral Koh J, Choi JR, Han KH et al (2013) Proper indication of BRAF V600E mutation testing in fine-needle aspirates of thyroid nodules. PLoS ONE 8:e64505CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Yoon M, Jung SJ, Kim TH et al (2016) Relationships between transporter expression and the status of BRAF V600E mutation and F-18 FDG uptake in papillary thyroid carcinomas. Endocr Res 41:64–69CrossRefPubMed Yoon M, Jung SJ, Kim TH et al (2016) Relationships between transporter expression and the status of BRAF V600E mutation and F-18 FDG uptake in papillary thyroid carcinomas. Endocr Res 41:64–69CrossRefPubMed
8.
Zurück zum Zitat Yoon S, An YS, Lee SJ et al (2015) Relation between F-18 FDG uptake of PET/CT and BRAFV600E mutation in papillary thyroid cancer. Med 94(48):e2063CrossRef Yoon S, An YS, Lee SJ et al (2015) Relation between F-18 FDG uptake of PET/CT and BRAFV600E mutation in papillary thyroid cancer. Med 94(48):e2063CrossRef
9.
Zurück zum Zitat Choi EK, Kim SH, Hyun OJ et al (2015) Preoperative 18F-FDG PET/CT as an indicator of clinicopathologic features and BRAFV600E mutation in patients with papillary thyroid cancer. J Nucl Med 56:1665 Choi EK, Kim SH, Hyun OJ et al (2015) Preoperative 18F-FDG PET/CT as an indicator of clinicopathologic features and BRAFV600E mutation in patients with papillary thyroid cancer. J Nucl Med 56:1665
10.
Zurück zum Zitat Yeo M-K, Liang ZL, Oh T et al (2011) Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules. Clin Endocrinol 75:555–560CrossRef Yeo M-K, Liang ZL, Oh T et al (2011) Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules. Clin Endocrinol 75:555–560CrossRef
11.
Zurück zum Zitat Vaccarella S, Franceschi S, Bray F et al (2016) Worldwide thyroid-cancer epidemic? The increasing impact of overdiagnosis. N Engl J Med 375:614–617CrossRefPubMed Vaccarella S, Franceschi S, Bray F et al (2016) Worldwide thyroid-cancer epidemic? The increasing impact of overdiagnosis. N Engl J Med 375:614–617CrossRefPubMed
12.
Zurück zum Zitat So Y, Chung HW, Kim SK et al (2015) Preoperative FDG PET/CT in papillary thyroid carcinoma for prediction of recurrence. J Nucl Med 56:1643 So Y, Chung HW, Kim SK et al (2015) Preoperative FDG PET/CT in papillary thyroid carcinoma for prediction of recurrence. J Nucl Med 56:1643
13.
Zurück zum Zitat Sturgeon C, Angelos P (2006) Identification and treatment of aggressive thyroid cancers. Part 2: risk assessment and treatment. Oncology (Williston Park) 20:397–404; discussion 404:407–398 Sturgeon C, Angelos P (2006) Identification and treatment of aggressive thyroid cancers. Part 2: risk assessment and treatment. Oncology (Williston Park) 20:397–404; discussion 404:407–398
14.
Zurück zum Zitat Renaud F, Gnemmi V, Devos P et al (2014) MUC1 expression in papillary thyroid carcinoma is associated with BRAF mutation and lymph node metastasis; the latter is the most important risk factor of relapse. Thyroid 24:1375–1384CrossRefPubMed Renaud F, Gnemmi V, Devos P et al (2014) MUC1 expression in papillary thyroid carcinoma is associated with BRAF mutation and lymph node metastasis; the latter is the most important risk factor of relapse. Thyroid 24:1375–1384CrossRefPubMed
15.
Zurück zum Zitat Lee X, Gao M, Ji Y et al (2009) Analysis of differential BRAF(V600E) mutational status in high aggressive papillary thyroid microcarcinoma. Ann Surg Oncol 16:240–245CrossRefPubMed Lee X, Gao M, Ji Y et al (2009) Analysis of differential BRAF(V600E) mutational status in high aggressive papillary thyroid microcarcinoma. Ann Surg Oncol 16:240–245CrossRefPubMed
16.
Zurück zum Zitat Xing MZ (2007) BRAF mutation in papillary thyroid cancer: pathogenic role, molecular bases, and clinical implications. Endocr Rev 28:742–762CrossRefPubMed Xing MZ (2007) BRAF mutation in papillary thyroid cancer: pathogenic role, molecular bases, and clinical implications. Endocr Rev 28:742–762CrossRefPubMed
17.
Zurück zum Zitat Lee DY, Hwang SM, An JH et al (2016) Predicting extrathyroidal extension in patients with papillary thyroid microcarcinoma according to a BRAF mutation. Clin Exp Otorhinolaryngol 10:174CrossRefPubMedPubMedCentral Lee DY, Hwang SM, An JH et al (2016) Predicting extrathyroidal extension in patients with papillary thyroid microcarcinoma according to a BRAF mutation. Clin Exp Otorhinolaryngol 10:174CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Tufano RP, Teixeira GV, Bishop J et al (2012) BRAF mutation in papillary thyroid cancer and its value in tailoring initial treatment: a systematic review and meta-analysis. Med (Baltimore) 91:274–286CrossRef Tufano RP, Teixeira GV, Bishop J et al (2012) BRAF mutation in papillary thyroid cancer and its value in tailoring initial treatment: a systematic review and meta-analysis. Med (Baltimore) 91:274–286CrossRef
20.
Zurück zum Zitat Viola D, Valerio L, Molinaro E et al (2016) Treatment of advanced thyroid cancer with targeted therapies: ten years of experience. Endocr Relat Cancer 23:R185–R205CrossRefPubMed Viola D, Valerio L, Molinaro E et al (2016) Treatment of advanced thyroid cancer with targeted therapies: ten years of experience. Endocr Relat Cancer 23:R185–R205CrossRefPubMed
21.
Zurück zum Zitat Lee WS, Palmer BJA, Garcia A et al (2014) BRAF mutation in papillary thyroid cancer: a cost-utility analysis of preoperative testing. Surgery 156:1569–1578CrossRefPubMed Lee WS, Palmer BJA, Garcia A et al (2014) BRAF mutation in papillary thyroid cancer: a cost-utility analysis of preoperative testing. Surgery 156:1569–1578CrossRefPubMed
22.
Zurück zum Zitat Lee SH, Han S, Lee HS et al (2016) Association between 18F-FDG avidity and the BRAF mutation in papillary thyroid carcinoma. Nucl Med Mol Imaging 50:38–45CrossRefPubMed Lee SH, Han S, Lee HS et al (2016) Association between 18F-FDG avidity and the BRAF mutation in papillary thyroid carcinoma. Nucl Med Mol Imaging 50:38–45CrossRefPubMed
23.
Zurück zum Zitat Salvatori M, Biondi B, Rufini V (2015) Imaging in endocrinology: 2-[18F]-fluoro-2-deoxy-d-glucose positron emission tomography/computed tomography in differentiated thyroid carcinoma: clinical indications and controversies in diagnosis and follow-up. Eur J Endocrinol 173:R115–130PubMed Salvatori M, Biondi B, Rufini V (2015) Imaging in endocrinology: 2-[18F]-fluoro-2-deoxy-d-glucose positron emission tomography/computed tomography in differentiated thyroid carcinoma: clinical indications and controversies in diagnosis and follow-up. Eur J Endocrinol 173:R115–130PubMed
24.
Zurück zum Zitat Seo JW, Hwang SH, Cho A et al (2016) Prognostic impact of ultrasonography features and 18F-fluorodeoxyglucose uptake in patients with papillary thyroid microcarcinoma. Clin Exp Otorhinolaryngol 9:62–69CrossRefPubMedPubMedCentral Seo JW, Hwang SH, Cho A et al (2016) Prognostic impact of ultrasonography features and 18F-fluorodeoxyglucose uptake in patients with papillary thyroid microcarcinoma. Clin Exp Otorhinolaryngol 9:62–69CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Virk RK, Van Dyke AL, Finkelstein A et al (2013) BRAFV600E mutation in papillary thyroid microcarcinoma: a genotype-phenotype correlation. Mod Pathol 26:62–70CrossRefPubMed Virk RK, Van Dyke AL, Finkelstein A et al (2013) BRAFV600E mutation in papillary thyroid microcarcinoma: a genotype-phenotype correlation. Mod Pathol 26:62–70CrossRefPubMed
27.
Zurück zum Zitat Zheng X, Wei S, Han Y et al (2013) Papillary microcarcinoma of the thyroid: clinical characteristics and BRAF(V600E) mutational status of 977 cases. Ann Surg Oncol 20:2266–2273CrossRefPubMed Zheng X, Wei S, Han Y et al (2013) Papillary microcarcinoma of the thyroid: clinical characteristics and BRAF(V600E) mutational status of 977 cases. Ann Surg Oncol 20:2266–2273CrossRefPubMed
28.
Zurück zum Zitat Walczyk A, Kowalska A, Kowalik A et al (2014) The BRAF(V600E) mutation in papillary thyroid microcarcinoma: does the mutation have an impact on clinical outcome? Clin Endocrinol (Oxf) 80:899–904CrossRef Walczyk A, Kowalska A, Kowalik A et al (2014) The BRAF(V600E) mutation in papillary thyroid microcarcinoma: does the mutation have an impact on clinical outcome? Clin Endocrinol (Oxf) 80:899–904CrossRef
29.
Zurück zum Zitat Soret M, Bacharach SL, Buvat I (2007) Partial-volume effect in PET tumor imaging. J Nucl Med 48:932–945CrossRefPubMed Soret M, Bacharach SL, Buvat I (2007) Partial-volume effect in PET tumor imaging. J Nucl Med 48:932–945CrossRefPubMed
30.
Zurück zum Zitat Choi SJ, Kim TY, Lee JC et al (2008) Is routine central neck dissection necessary for the treatment of papillary thyroid microcarcinoma? Clin Exp Otorhinolaryngol 1:41–45CrossRefPubMedPubMedCentral Choi SJ, Kim TY, Lee JC et al (2008) Is routine central neck dissection necessary for the treatment of papillary thyroid microcarcinoma? Clin Exp Otorhinolaryngol 1:41–45CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Kang KW, Kim S-K, Kang H-S et al (2003) Prevalence and risk of cancer of focal thyroid incidentaloma identified by 18F-fluorodeoxyglucose positron emission tomography for metastasis evaluation and cancer screening in healthy subjects. J Clin Endocrinol Metab 88:4100–4104CrossRefPubMed Kang KW, Kim S-K, Kang H-S et al (2003) Prevalence and risk of cancer of focal thyroid incidentaloma identified by 18F-fluorodeoxyglucose positron emission tomography for metastasis evaluation and cancer screening in healthy subjects. J Clin Endocrinol Metab 88:4100–4104CrossRefPubMed
Metadaten
Titel
Relationship Between 18F-fluorodeoxyglucose Accumulation and the BRAF V600E Mutation in Papillary Thyroid Cancer
verfasst von
Jae Won Chang
Ki Wan Park
Jae Hyung Heo
Seung-Nam Jung
Lihua Liu
Sung Min Kim
In Sun Kwon
Bon Seok Koo
Publikationsdatum
14.08.2017
Verlag
Springer International Publishing
Erschienen in
World Journal of Surgery / Ausgabe 1/2018
Print ISSN: 0364-2313
Elektronische ISSN: 1432-2323
DOI
https://doi.org/10.1007/s00268-017-4136-y

Weitere Artikel der Ausgabe 1/2018

World Journal of Surgery 1/2018 Zur Ausgabe

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

CME: 2 Punkte

Prof. Dr. med. Gregor Antoniadis Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

CME: 2 Punkte

Dr. med. Benjamin Meyknecht, PD Dr. med. Oliver Pieske Das Webinar S2e-Leitlinie „Distale Radiusfraktur“ beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

CME: 2 Punkte

Dr. med. Mihailo Andric
Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.