ClinicalTrials.Veeva

Menu

RET Inhibitor for Neoadjuvant Therapy in Locally Advanced RET-altered Thyroid Cancer

Fudan University logo

Fudan University

Status

Enrolling

Conditions

Thyroid Cancer

Treatments

Procedure: Surgery
Drug: RET Inhibitor

Study type

Observational

Funder types

Other

Identifiers

NCT06530316
PATHYOID

Details and patient eligibility

About

This study is a multicenter observational study. Patients receive neoadjuvant therapy with RET inhibitors in the real world, and those who can undergo surgery after neoadjuvant therapy receive surgical treatment. The aim of the study is to determine the efficacy and safety of RET inhibitors for neoadjuvant therapy in locally advanced RET-altered thyroid cancer.

Enrollment

48 estimated patients

Sex

All

Ages

14 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients voluntarily join this study and sign an informed consent form;

  • Age: ≥ 14 years old, male or female not limited;

  • Locally advanced thyroid cancer diagnosed by histopathology, including papillary thyroid carcinoma, medullary thyroid carcinoma, follicular thyroid carcinoma, poorly differentiated/poorly differentiated thyroid carcinoma, etc;

  • RET alterations, including fusion and mutations;

  • The definition of locally advanced thyroid cancer meets at least one of the following criteria:

    1. Local advanced thyroid cancer with estimated surgical difficulty and inability to R0/1 resection;
    2. T4 thyroid cancer defined by AJCC: any size of tumor primary lesion or regional lymph node infiltration beyond the thyroid capsule to subcutaneous soft tissue, larynx, trachea, esophagus, or recurrent laryngeal nerve, tumor invasion of pre vertebral fascia or wrapping around carotid or mediastinal blood vessels;
    3. According to the imaging score, the resectable probability is less than 80% based on CT.
  • At least one measurable lesion;

  • For patients with distant metastasis, researchers need to determine whether patients would benefit from surgery;

  • Patients voluntarily undergo tumor tissue biopsy/surgery during enrollment and withdrawal;

  • Normal function of major organs.

Exclusion criteria

  • Previously used RET inhibitors;
  • There are multiple factors that affect the absorption of oral medication, such as inability to swallow, nausea and vomiting, chronic diarrhea, and intestinal obstruction;
  • The patient refuses to undergo tumor tissue biopsy or surgery;
  • Patients who are unsuitable for RET inhibitors or surgery.

Trial design

48 participants in 2 patient groups

None MTC
Description:
DTC, PDTC and ATC patients with RET fusions.
Treatment:
Drug: RET Inhibitor
Procedure: Surgery
MTC
Description:
MTC patients with RET mutations
Treatment:
Drug: RET Inhibitor
Procedure: Surgery

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems