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Construction and validation of a nomogram for predicting cervical lymph node metastasis in diffuse sclerosing variant of papillary thyroid carcinoma

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Abstract

Objective

To analyze the risk factors associated with the occurrence of cervical lymph node metastasis (LNM) in patients with diffuse sclerosing variant of papillary thyroid carcinoma (DSV-PTC) and to establish a nomogram model.

Methods

Clinical data of 199 DSV-PTC patients from SEER database were obtained, and they were randomly divided into training group (n=139) and validation group (n=60). The clinicopathological characteristics were analyzed by logistic regression, including age, marital status, race, gender, tumor size(cm), T stage, M stage, bilaterality, capsular invasion, extrathyroidal extension (ETE), and multifocality. The Validation was carried out using C-index, calibration curves, and Decision Curve Analysis (DCA) in terms of differentiation and calibration of the nomogram model, respectively.

Results

Age, tumor size(cm), capsular invasion, and multifocality were independent risk factors for the development of LNM in patients with DSV-PTC (P<0.05). In the training and validation groups, the C-index of internal validation of the nomogram was 0.808 (95%CI: 0.733-0.755) and 0.813 (95% CI: 0.591-0.868), the calibration curves showed that the model was in good agreement, and the decision curve (DCA) indicated that the nomogram model had good clinical utility. 

Conclusion

Age, tumor size(cm), capsular invasion, and multifocality are independent risk factors for the development of LNM in DSV-PTC. The nomogram model can predict the risk of develo** LNM in DSV-PTC patients and provide clinical guidance.

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References

  1. Jung CK, Bychkov A, Kakudo K (2022) Update from the 2022 world health organization classification of thyroid tumors: A standardized diagnostic approach. Endocrinol Metab (Seoul, Korea) 37:703–718

    Article  CAS  Google Scholar 

  2. Limaiem F, Rehman A, Anastasopoulou C, Mazzoni T, Papillary Thyroid Carcinoma. In StatPearls, StatPearls Publishing Copyright © 2023, StatPearls Publishing LLC.: Treasure Island (FL) ineligible companies. Disclosure: Anis Rehman declares no relevant financial relationships with ineligible companies. Disclosure: Catherine Anastasopoulou declares no relevant financial relationships with ineligible companies. Disclosure: Thomas Mazzoni declares no relevant financial relationships with ineligible companies., 2023.

  3. Haugen BR, Alexander EK, Bible KC et al (2016) American Thyroid Association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American Thyroid Association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid : Official J Am Thyroid Assoc 26:1–133

    Article  Google Scholar 

  4. Vickery AL Jr, Carcangiu ML, Johannessen JV, Sobrinho-Simoes M (1985) Papillary carcinoma. Semin Diagnostic Pathol 2:90–100

    Google Scholar 

  5. Spinelli C, Strambi S, Bakkar S et al (2020) Surgical management of diffuse sclerosing variant of papillary thyroid carcinoma. Experience in 25 patients. World J Surg 44:155–162

    Article  PubMed  Google Scholar 

  6. Coca-Pelaz A, Shah JP, Hernandez-Prera JC et al (2020) Papillary thyroid cancer—Aggressive variants and impact on management: A narrative review. Adv Ther 37:3112–3128

    Article  PubMed  PubMed Central  Google Scholar 

  7. Fang H, Si Y, Wang C et al (2021) Diffuse intrathyroidal dissemination of papillary thyroid carcinoma with no stromal fibrosis at presentation: A pattern of aggressive differentiated thyroid carcinoma. Pathol Res Pract 224:153510

    Article  CAS  PubMed  Google Scholar 

  8. Jung HK, Hong SW, Kim EK, Yoon JH, Kwak JY (2013) Diffuse sclerosing variant of papillary thyroid carcinoma: sonography and specimen radiography. J Ultrasound Med 32:347–354

    Article  PubMed  Google Scholar 

  9. Pizzimenti C, Fiorentino V, Ieni A et al (2022) Aggressive variants of follicular cell-derived thyroid carcinoma: an overview. Endocrine 78:1–12

    Article  CAS  PubMed  Google Scholar 

  10. You E, Mascarella MA, Al Jassim A et al (2019) Prevalence and aggressiveness of papillary thyroid carcinoma in surgically-treated graves' disease patients: a retrospective matched cohort study. J Otolaryngol-Head Neck Surg 48:40

    Article  PubMed  PubMed Central  Google Scholar 

  11. Takagi N, Hirokawa M, Nobuoka Y et al (2014) Diffuse sclerosing variant of papillary thyroid carcinoma: a study of fine needle aspiration cytology in 20 patients. Cytopathology 25:199–204

    Article  CAS  PubMed  Google Scholar 

  12. Wang X, Xu F, Gao J et al (2022) Differential diagnosis of diffuse sclerotic thyroid papillary carcinoma and Hashimoto's thyroiditis using fine-needle aspiration cytology, BRAF(V600E) , and ultrasound elastography. J Clin Ultrasound : JCU 50:942–950

    Article  PubMed  Google Scholar 

  13. Rhoden KJ, Unger K, Salvatore G et al (2006) RET/papillary thyroid cancer rearrangement in nonneoplastic thyrocytes: follicular cells of Hashimoto's thyroiditis share low-level recombination events with a subset of papillary carcinoma. J Clin Endocrinol Metab 91:2414–2423

    Article  CAS  PubMed  Google Scholar 

  14. Sheu SY, Schwertheim S, Worm K, Grabellus F, Schmid KW (2007) Diffuse sclerosing variant of papillary thyroid carcinoma: lack of BRAF mutation but occurrence of RET/PTC rearrangements. Modern Pathol 20:779–787

    Article  CAS  Google Scholar 

  15. Joung JY, Kim TH, Jeong DJ et al (2016) Diffuse sclerosing variant of papillary thyroid carcinoma: major genetic alterations and prognostic implications. Histopathology 69:45–53

    Article  PubMed  Google Scholar 

  16. Rocha AS, Soares P, Seruca R et al (2001) Abnormalities of the E-cadherin/catenin adhesion complex in classical papillary thyroid carcinoma and in its diffuse sclerosing variant. J Pathol 194:358–366

    Article  CAS  PubMed  Google Scholar 

  17. Kinoshita Y, Takasu K, Yuri T et al (2013) Estrogen receptor- and progesterone receptor-positive diffuse sclerosing variant of papillary thyroid carcinoma: a case report. Case Rep Oncol 6:216–223

    Article  PubMed  PubMed Central  Google Scholar 

  18. Uysal S, Toker A, Türkmen K, Keskin S (2023) The role of decoy receptor 3 in inflammation and atherosclerosis in patients with chronic kidney disease and renal transplant patients. Nefrologia 43:344–350

    Article  PubMed  Google Scholar 

  19. Chang WC, Chen JY, Lee CH, Yang AH (2013) Expression of decoy receptor 3 in diffuse sclerosing variant of papillary thyroid carcinoma: correlation with M2 macrophage differentiation and lymphatic invasion. Thyroid 23:720–726

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Crayton H, Wu K, Leong D et al (2023) Diffuse sclerosing variant papillary thyroid carcinoma has worse survival than classic papillary thyroid carcinoma: a meta-analysis. Endocr Relat Cancer 30(6):e220348

  21. Zanoni DK, Patel SG, Shah JP (2019) Changes in the 8th edition of the American Joint Committee on Cancer (AJCC) staging of head and neck cancer: rationale and implications. Curr Oncol Rep 21(6):52

  22. Koo JS, Hong S, Park CS (2009) Diffuse sclerosing variant is a major subtype of papillary thyroid carcinoma in the young. Thyroid 19:1225–1231

    Article  PubMed  Google Scholar 

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Funding

This work was supported by the Natural Science Foundation of Hebei Province (H2020307028).

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Correspondence to Fenghua Zhang.

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Lin, X., Huo, J., Zhang, H. et al. Construction and validation of a nomogram for predicting cervical lymph node metastasis in diffuse sclerosing variant of papillary thyroid carcinoma. Langenbecks Arch Surg 409, 8 (2024). https://doi.org/10.1007/s00423-023-03178-8

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