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Survival Nomogram for Patients With Thymic Carcinoma

Survival Nomogram for Patients With Thymic Carcinoma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07179341
Enrollment
156
Registered
2025-09-17
Start date
2024-07-09
Completion date
2025-08-01
Last updated
2025-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thymic Carcinoma

Brief summary

Background Thymic carcinoma (TC) is a rare and aggressive mediastinal malignancy with poor prognosis. Our study aimed to develop a nomogram to predict overall survival (OS) of TC patients. Method A total of 156 patients confirmed TC between 1996 and 2023 were selected from our database. They were divided into training cohort, validation cohort one and validation cohort two. A nomogram was constructed based on the risk factors affecting prognosis using a Cox proportional hazards regression model. The discrimination and calibration of the nomogram were evaluated by C-index, AUC and curve of calibration. The three cohorts were divided into low-risk and high-risk subgroups.

Interventions

PROCEDUREThymectomy for thymic carcinoma

Thymectomy for thymic cancer

Sponsors

Weijie Ye
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* The diagnosis of TC in patients should be confirmed through endoscopic tumor biopsy or surgery to obtain tumor tissue for pathological confirmation under light microscope, and even further confirmed through immunohistochemical staining. * Patients should accept surgery and obtain complete postoperative pathological reports in order to assess Masaoka-Koga staging. * Patients who accepted surgery should be followed up at least six months or reached the endpoint event.

Exclusion criteria

* The patient had two types of primary tumors concurrently including TC. * The tumor in the thymus was not primary but metastatic, having originated from a different primary site. * The patient did not obtain a complete pathological report after surgery.

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalFrom date of accepting surgery until the date of final documented or date of death from any cause, whichever came first, assessed up to 325 monthsOverall survival (OS) is the length of time a patient lives after a diagnosis or the start of treatment for a disease, such as cancer

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026