GETNE Registration of Thyroid Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGrupo Espanol de Tumores Neuroendocrinos

About this trial

An epidemiological, observational, multicenter, cross-sectional, retrospective study on patients ≥ 18 years visited in the oncology services of the participating centers with diagnosis of primary thyroid cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients older than 18 years with diagnosis of differentiated, medullary or anaplastic thyroid cancer confirmed by histopathology.

Patients who agree to participate and are able to understand the information sheet and sign the informed consent

Disqualifiers

Patients under 18 years of age.

Patients with other types of thyroid cancer or whose histopathological diagnosis has not been confirmed.

Patients who do not have the relevant basic information to be included in the study, according to the criteria of the principal investigator.

Trial population

Patients ≥ 18 years visited in the oncology services of the participating centers that have a diagnosis of primary cancer located in the thyroid gland.

Trial design

Design model

Ecologic or community

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Hystopathological characteristics of the tumor

Based on pathologist evaluation of biopsy including differentiated, medullar or anaplasic.

Time frame
Baseline
2

Situation of the tumor at first-diagnosis

Local tumor, locoregional tumor or metastatic disease.

Time frame
Baseline
3

Tumor-Node-Metastasis classification

Based on the AJCC (American Joint Committee on Cancer) 2018 TNM system: T for extent or size of the tumor, N for lymph nodes spread and M for metastasis.

Time frame
Baseline
4

Tumor Stage

From I to IV, based on the interpretation of the TNM classification and depending on the hystopathological characteristics of the tumor.

Time frame
Baseline

Secondary outcomes

1

Patient situation at the end of treatment

Results of clinical evaluation of the disease including complete response, partial response, stable disease, progression of disease or death

Time frame
12 months
2

Number of patients with BRAF mutation

Total patients with available results on BRAF status and proportion of patients with mutated BRAF or native BRAF.

Time frame
12 months
3

Number of patients with RET mutation

Total patients with available results on RET status and proportion of patients with mutated RET or native RET.

Time frame
12 months
4

Number of patients with PI3K mutation

Total patients with available results on PI3K status and proportion of patients with mutated PI3K or native PI3K.

Time frame
12 months

Other outcomes

Sponsors and contacts

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