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Molecular Analysis and Treatment Options of Thymic Malignancies

Molecular Landscape Analysis and Treatment Options for Thymic Epithelial Tumors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05667948
Enrollment
500
Registered
2022-12-29
Start date
2016-01-01
Completion date
2026-12-31
Last updated
2025-05-22

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

Conditions

Thymic Cancer, Thymic Carcinoma, Thymic Epithelial Tumor

Keywords

thymic malignancy, thymoma, chemotherapy, targeted therapy, immunotherapy, molecular landscape

Brief summary

Thymic malignancies are the most common tumors of the anterior mediastinum, though surgery and radiation often effectively treat thymic carcinomas, a minority continue to progress and eventually lead to death. Therefore, there is an unmet need for more effective therapies for thymic malignancies. Considering the role of molecular alterations has yet to be defined in the treatment of thymoma and thymic malignancies, there is an urgent recognition that molecular alterations in the thymic malignancies are important to predict response and survival for novel targeted therapies. In summary, identification of genetic alterations in thymic malignancies is increasingly essential to perform molecular diagnostics and individualized treatments. This project aims to create a registry of patients with thymic malignancies to further the characterization of molecular alterations and develop (novel) treatments based on the detection.

Interventions

DRUGChemotherapy

different treatments based on the molecular analysis

Sponsors

Shanghai Chest Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologically proven diagnosis of thymic malignancies * 18 years of age or older * Ability to understand and the willingness to sign a written informed consent document

Design outcomes

Primary

MeasureTime frameDescription
Objective response rate (ORR)20 yearsCollect detailed clinical information on patients with thymic malignancies via the electronic medical records
Disease control rate (DCR)20 yearsCollect detailed clinical information on patients with thymic malignancies via the electronic medical records
Progression-free survival (PFS)20 yearsCollect detailed clinical information on patients with thymic malignancies via the electronic medical records

Secondary

MeasureTime frameDescription
Overall survival (OS)20 yearsCollect detailed clinical information on patients with thymic malignancies via the electronic medical records

Countries

China

Outcome results

None listed

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