Oncology

Thymoma and Thymic Carcinoma

Also known as thymic epithelial tumor, WHO type A-B3 thymoma, thymic carcinoma

Thymoma and thymic carcinoma are rare thymic epithelial tumours classified by WHO histological subtype (A, AB, B1, B2, B3 for thymomas, and C for thymic carcinoma), with markedly differing biology and prognosis across the spectrum. Thymomas

ORPHA:99870 ↗Prevalence 1.5–1.7 in 1,000,000Onset Adult (median age 50s for thymoma; 40s–50s for thymic carcinoma)Sporadic

19

studies recruiting now

as of 7 Sept 2026

89

studies registered in total

as of 7 Sept 2026

2

countries with a recruiting site

as of 7 Sept 2026

7 Jan 2026

most recent study posted

among recruiting studies

Recruiting trials

Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.

See all 19 recruiting studies

Where recruiting studies are running

Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.

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Patient organisations

Thymic Carcinoma FoundationPatient association
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About Thymoma and Thymic Carcinoma

Thymoma and thymic carcinoma are rare thymic epithelial tumours classified by WHO histological subtype (A, AB, B1, B2, B3 for thymomas, and C for thymic carcinoma), with markedly differing biology and prognosis across the spectrum. Thymomas are characterised by their unique association with autoimmune disorders — most notably myasthenia gravis, which occurs in 30–50% of thymoma patients — as well as pure red cell aplasia and hypogammaglobulinaemia. Thymic carcinoma lacks these paraneoplastic associations but is typically more aggressive, with higher rates of distant metastasis and a paucity of effective second-line systemic therapies following platinum-based chemotherapy.

Common clinical features

Anterior mediastinal mass discovered incidentally on chest imaging or causing chest pain, dyspnoea, and superior vena cava syndromeMyasthenia gravis: fatigable muscle weakness, ptosis, diplopia, dysphagia, and respiratory compromisePure red cell aplasia presenting as severe, transfusion-dependent anaemiaHypogammaglobulinaemia (Good's syndrome) causing recurrent bacterial infectionsChest pain or phrenic nerve palsy from locally advanced diseasePleural or pericardial metastatic effusionDistant metastases to bone, liver, and extrathoracic lymph nodes in thymic carcinoma

From Orphanet’s phenotype annotations (CC BY 4.0). Not a complete list.

Treatments being studied

11 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.

Phase 2Sacituzumab Govitecan (Trodelvy)
Phase 2Pemetrexed Disodium (Alimta)
Phase 2Sunitinib (Sunitinib accord)
Phase 2Sacituzumab Tirumotecan
Phase 2Ivonescimab
Phase 2Erfonrilimab
Phase 2Avelumab (Bavencio)
Phase 2Belinostat (Beleodaq)

+ 3 more in development

Before you apply

Things trial teams commonly ask about for Thymoma and Thymic Carcinoma. Not eligibility rules; those are set by each study.

  • WHO histological subtype (A/AB/B1/B2/B3 thymoma versus thymic carcinoma) is a key eligibility and stratification criterion — confirm the exact subtype is documented in the pathology report with expert review if necessary.
  • Myasthenia gravis status and its treatment (acetylcholinesterase inhibitors, immunosuppressants, thymectomy history) must be disclosed as checkpoint inhibitors can precipitate severe myasthenic crisis and are often contraindicated or require close monitoring.
  • Prior lines of platinum-based chemotherapy and recurrence status (resectable vs. unresectable/metastatic) determine eligibility for most second-line trials; provide a complete treatment chronology with response assessments.

Related conditions

Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).