# Precision management of medullary thyroid carcinoma: a dynamic framework integrating biomarkers, genotyping, and risk stratification

**Authors:** Chengzheng Jia, Shaohua Guo, Kehui Wu, Yaoqi Wang, Shuai Yang, Lei Wang, Tianyu Chen, Xianying Meng

PMC · DOI: 10.3389/fendo.2026.1794118 · Frontiers in Endocrinology · 2026-03-05

## TL;DR

This paper presents a framework for managing medullary thyroid carcinoma by integrating biomarkers, genetic testing, and risk factors to guide personalized treatment decisions.

## Contribution

The paper introduces a three-panel clinical workflow integrating germline RET testing, biomarker kinetics, and postoperative risk factors for precision MTC management.

## Key findings

- Germline RET testing is mandated for all MTC patients to distinguish hereditary from sporadic disease.
- Desmoplastic stromal reaction is identified as a postoperative risk modifier in sporadic MTC.
- A staged approach for sporadic MTC uses imaging and biochemical response to tailor surveillance and intervention.

## Abstract

Medullary thyroid carcinoma (MTC) is a heterogeneous neuroendocrine malignancy in which outcomes are shaped by tumor burden, locoregional spread, and molecular context. Precision management therefore requires explicit separation of hereditary MTC driven by germline RET variants from presumed sporadic disease, and a structured integration of serum biomarkers, imaging, pathology, and genotype. This review synthesizes actionable evidence on calcitonin (Ctn) and carcinoembryonic antigen (CEA) baseline values and kinetics, universal germline RET testing, and tumor somatic profiling in advanced or progressive disease, and highlights desmoplastic stromal reaction (DSR) as an underused postoperative risk modifier in sporadic MTC. We propose a clinician-facing three-panel workflow: Panel A standardizes initial evaluation and mandates germline RET testing for all patients; Panel B outlines genotype- and staging-informed surgery and surveillance for hereditary disease, including pediatric carriers; and Panel C provides a staged approach for sporadic MTC in which imaging directs compartment selection and early postoperative DSR and biochemical response tailor surveillance intensity and thresholds for re-staging and re-intervention. By aligning decision nodes with real-world scenarios and using consistent surgical terminology, this framework offers a testable blueprint for precision surgery, surveillance stratification, and genotype-directed systemic therapy.

## Linked entities

- **Genes:** RET (ret proto-oncogene) [NCBI Gene 5979]
- **Proteins:** Calca (calcitonin-related polypeptide alpha)
- **Diseases:** medullary thyroid carcinoma (MONDO:0007958)

## Full-text entities

- **Genes:** TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, CHGA (chromogranin A) [NCBI Gene 1113] {aka CGA, PHE5, PHES}, TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, NF1 (neurofibromin 1) [NCBI Gene 4763] {aka NFNS, VRNF, WSS}, HRAS (HRas proto-oncogene, GTPase) [NCBI Gene 3265] {aka C-BAS/HAS, C-H-RAS, C-HA-RAS1, CTLO, H-RASIDX, HAMSV}
- **Diseases:** thyroid cancer (MESH:D013964), node (MESH:D012804), nodal (MESH:D013611), neuroendocrine malignancy (MESH:D018358), DSR (MESH:D018220), metastases (MESH:D009362), lateral disease (MESH:D004194), MEN2 (MESH:D018813), malignancy (MESH:D009369), renal dysfunction (MESH:D007674), ATA (MESH:D001260), hereditary and sporadic disease (MESH:D001943), lymph node metastasis (MESH:D008207), sporadic disease (MESH:D020821), MTC (MESH:C536914), hereditary disease (MESH:D030342)
- **Chemicals:** anlotinib (MESH:C000625192), selpercatinib (MESH:C000656166), cabozantinib (MESH:C558660), eosin (MESH:D004801), hematoxylin (MESH:D006416), vandetanib (MESH:C452423), radioiodine (MESH:C000614965), pralsetinib (MESH:C000655704)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** M918T

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12980077/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12980077/full.md

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Source: https://tomesphere.com/paper/PMC12980077