Adjuvant Radiotherapy for Stage II/III Thymoma After Complete Resection

  • STATUS
    Recruiting
  • End date
    Dec 22, 2029
  • participants needed
    238
  • sponsor
    Fudan University
Updated on 22 January 2021
renal function
thymic neoplasm

Summary

This study is designed to investigate whether adjuvant radiotherapy after complete resection has a better survival for stage II or III thymoma.

Description

It is confirmed by many studies that patients of thymoma with complete resection have better prognosis than those with either incomplete resection or without surgery. However,whether patients with stage II or III thymoma could benefit from adjuvant radiotherapy after complete resection remains controversial. The purpose of this study is to investigate whether adjuvant radiotherapy after complete resection can improve survival for stage II or III thymoma.

Details
Condition Thymoma, Thymoma, Thymomas, thymic neoplasm
Treatment Adjuvant radiotherapy
Clinical Study IdentifierNCT02633553
SponsorFudan University
Last Modified on22 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

~75 years old; Eastern Cooperative Oncology Group performance status of 0 to
Pathologically confirmed masaoka stage II or III thymoma; Have adequate
bone marrow, hepatic, and renal function; Patients receive complete resection
within 3 months; Written informed consent

Exclusion Criteria

Patients with distant metastases; Patients underwent radiotherapy or
chemotherapy; Patients who have malignancy history excluding carcinoma in situ
of cervix in the previous five years; Active clinical pulmonary infection
Pregnant or nursing
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note