Skip to content

Adjuvant Hypofractionation Radiotherapy for Thymic Epithelial Tumours After Complete Resection

Adjuvant Hypofractionation Radiotherapy for Thymic Epithelial Tumours After Complete Resection-Single Center Phase II Single Arm Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06189183
Enrollment
50
Registered
2024-01-03
Start date
2023-11-11
Completion date
2040-12-31
Last updated
2026-06-16

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

Conditions

Thymus Neoplasms

Keywords

Thymus Neoplasms, Adjuvant Radiotherapy

Brief summary

The purpose of this study is to evaluate the efficiency and toxicity of adjuvant hypofractionation radiotherapy for thymic epithelial tumours after complete resection.

Detailed description

Adjuvant Radiotherapy(Postoperative radiotherapy) is proposed in stage II and III thymic carcinoma,stage III thymoma,stage IIB B2/B3 thymomas. Hypofractionation Radiotherapy is used in this study. The purpose of this study is to evaluate the efficiency and toxicity of adjuvant hypofractionation radiotherapy for thymic epithelial tumours after complete resection.

Interventions

RADIATIONAdjuvant Hypofractionation Radiotherapy

Adjuvant Hypofractionation Radiotherapy for Thymic Epithelial Tumours After Complete Resection

Sponsors

Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Adjuvant Hypofractionation Radiotherapy for Thymic Epithelial Tumours After Complete Resection

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Thymoma and Thymic carcinoma confirmed by histology or cytology * R0 resection (complete resection) * stage II and III thymic carcinoma,stage III thymoma,stage IIB B2/B3 thymomas. * Karnofsky performance status(KPS) 80, 90 or 100. * Having sufficient Pulmonary function, renal function and liver function. Neutrophile granulocyte count\>1.5×109 /L, platelet count\>80×109 /L, hemoglobin ≥10g/dL.

Exclusion criteria

* Prior thoracic radiotherapy. * Uncontrolled Comorbidities. * Pregnant or nursing mother. * Pneumonia

Design outcomes

Primary

MeasureTime frameDescription
Disease Free Survival2 years, 5 yearsFrom the date of resection to the date of disease recurrence or death

Secondary

MeasureTime frameDescription
Overall Survival2 years, 5 yearsFrom the date of resection to the date of death
RadiotherapyToxicity1 years, 2 years, 5 yearsRate of pneumonitis;Rate of esophagitis;Rate of skin reaction;Rate of myelitis;Rate of heart disease;Rate of vascular toxicity
local recurrence2 years, 5 yearsrecurrence of tumor bed
Intrathoracic recurrence / pleural metastasis2 years, 5 yearsRate of Intrathoracic recurrence / pleural metastasis
metastasis free survival2 years, 5 yearsFrom the date of resection to the date of metastasis or death

Countries

China

Contacts

PRINCIPAL_INVESTIGATORTao Zhang, Dr.

National Cancer Center/Cancer Hospital, CAMS

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026