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Postoperative Conformal Radiotherapy for Stage II-III B Type Thymoma

A Multi-institutional, Randomized Controlled Trial of Postoperative Conformal Radiotherapy for Stage II-III B Type Thymoma

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02014805
Enrollment
210
Registered
2013-12-18
Start date
2013-07-31
Completion date
2022-07-31
Last updated
2020-07-16

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

Conditions

Thymoma

Keywords

postoperative, conformal, radiotherapy, thymoma

Brief summary

The purpose of this study is to determine whether postoperative conformal radiotherapy are effective in the treatment of Masaoka stage II-III B type thymoma.

Detailed description

The role of postoperative radiotherapy in thymoma is controversial. Some retrospective studies were for the radiotherapy, but others were against. However, more inherent biases existed in these trials. Resection, Masaoka stage and pathology were widely accepted as the prognostic factors for thymoma. Furthermore, the frequency of local failure after radical resection was still high in Masaoka stage II-III B type thymoma. With the conformal technique appearing, conformal radiotherapy can escalate the dose without increasing the risk of normal tissue toxicities.

Interventions

RADIATIONradiotherapy

postoperative conformal radiotherapy for Masaoka stage II-III B type thymoma

Sponsors

Beijing Hospital
CollaboratorOTHER_GOV
309th Hospital of Chinese People's Liberation Army
CollaboratorOTHER
Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Age 18-75, Zubrod-ECOG-WHO 0-2, the interval of surgery to radiotherapy \< 2months, Masaoka stage II-III and WHO B type thymoma

Exclusion criteria

* No second primary tumor, no serious comorbidity, no neoadjuvant anticancer treatment, no adjuvant chemotherapy.

Design outcomes

Primary

MeasureTime frameDescription
3 year local control rate3 year after the end of all enrollmentlocal control: tumor recurrence in the tumor bed 3 year local control rate: number of patients with tumor recurrence in the tumor bed at 3 years

Secondary

MeasureTime frameDescription
3 year failure-free and overall survival3 year after the end of all enrollmentfailure-free survivail: the interval from the surgery and the recurrence within or out the tumor bed overall survival: the interval from the surgery and the death or lost of follow-up

Other

MeasureTime frameDescription
rate of acute and late radiation toxicitywithin 3 year after the end of all enrollmenttoxicity: including the acute radition-induced lung toxicity and the late lung toxicity at 1, 3, 6, 9, 12, 18, 24, 30 and 36 month after radiation or observation
quality of life scorewithin 3 years after all enrollmentquality of life: FACT-Lung and EORTC QOL C30 before and after radiation, and at 1, 3, 6, 9, 12, 18, 24, 30, 36 months after radiation or observation

Countries

China

Contacts

Primary ContactQinfu Feng, M.D.
13811300221@163.com8610-87788503
Backup ContactYe Zhang, M.D.
drzye1983@163.com8610-87788504

Outcome results

None listed

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