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NCT Number: NCT06692062

Hypofractionated Radiotherapy for Thymic Epithelial Tumors

The goal of this clinical trial is to learn if hypofractionated radiotherapy works to shorten the treatment time without increasing the side effects in patients of thymic epithelial tumors. The main questions it aims to answer are:

* Does Hypofractionated radiotherapy provide better results? * Can hypofractionated radiotherapy reduce toxic and side effects compared with conventional radiotherapy? Researchers will compare the efficacy and safety of hypofractionated radiotherapy after thymic tumor surgery.

Participants will:

* Receive hypofractionated radiotherapy or conventional radiotherapy * Visit the hospital regularly once every 12 weeks for checkups and tests

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Xiangya Hospital, Central South University

Changsha, Hunan, 410000, China

Location status: Recruiting

Location contact

Rongrong Zhou, MD, PHD

CONTACT

[email protected]

+8613875898127

About this study

According to the World Health Organization histological classification system, thymic epithelial tumors (TET) are divided into thymoma and thymic carcinoma. Surgery is the main treatment for thymic tumors, and radiotherapy (RT), as an important auxiliary method of surgery, also plays an irreplaceable role in all stages of thymoma.

Hypofractionated radiotherapy is a common mode of radiotherapy for thoracic tumors. Unlike conventional radiotherapy, hypofractionated radiotherapy has a higher single dose and a shorter course of treatment. Because it improves the treatment efficiency, it can reduce the treatment time of patients and medical institutions and the cost of patients.

In the postoperative radiotherapy stage, conventional radiotherapy and hypofractionated radiotherapy were used. The course of hypofractionated radiotherapy was shorter than that of conventional radiotherapy. Patients chose to accept hypofractionated radiotherapy as the hypofractionated group, but not the conventional group.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients must provide written informed consent.
  • 18 years old ≤ age <75 years old.
  • Thymoma confirmed by pathology: type A, type AB, type B1, type B2, type B3. Thymic carcinoma. Patients with previous thymectomy were required to have complete surgical related data.
  • Masaoka⁃Koga ⁃ stage Ⅰ-Ⅲ
  • ECOG performance status 0-2.
  • Expected survival time > 1 year.
  • Participants of childbearing age must agree to use effective contraception during the trial; In women of childbearing age, a serum or urine pregnancy test must be negative.
  • Patients who are not lactating.
  • Sufficient bone marrow reserve and good function of important organs.

Exclusion criteria

  • patients with prior thoracic radiotherapy;
  • diseases not suitable for radiotherapy, such as recent myocardial infarction, active congestive heart failure;
  • Uncontrolled infectious disease or other serious medical or mental illness that may interfere with care
  • Patients with other malignant tumors that are not under stable control;
  • Known history of mental illness, substance abuse, alcohol or drug abuse.
  • Other conditions deemed unsuitable for enrollment by the attending physician.

Treatment and study plan

Hypofractionated Radiation Therapy

Radiation

R0 resection: 45-50Gy/20-25f R1 resection: 54-56Gy/25-28f R2 resection: 60-70Gy/30-35f

Primary outcomes

  1. 3-year PFS

    Time frame: The patients were followed up for 3 years from enrollment to disease progression or death.

    Time from enrollment to disease progression or death.

Secondary outcomes

  1. toxicity

    Time frame: Patients were followed from enrollment until 3 years.

    Any adverse medical event that occurred between the time the patient provided informed consent and was enrolled in the trial and the date of the last follow-up visit.

  2. 3-year OS

    Time frame: The patients were followed up for 3 years from enrollment to death.

    Time from patient enrollment to patient death.

Study contacts

Contact information is provided by the study sponsor or research team.

Rongrong Zhou, MD, PHD

CONTACT

[email protected]

+8613875898127

Sponsors and collaborators

Lead sponsor

Rongrong Zhou

Other

Registry information

Official study title

A Prospective Study of Hypofractionated Radiotherapy for Thymic Epithelial Tumors

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Nov 18, 2024
Registry last updated
Nov 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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