Safety and Efficacy of SBRT in the Reirradiation for Ultra-central Thoracic Malignant Tumors

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Observational
SUMMARY

The reirradiation of thoracic tumor is difficult. The possibility of surgery or re course radiotherapy is very small. In the NCCN guideline, only systemic treatment is recommended. However, the effective rate of systemic treatment is low. SBRT has the characteristics of high dose in tumor target area and low dose in surrounding normal tissues. In theory, SBRT is more conducive to the protection of normal tissues and can potentially be used in the salvage treatment of recurrent lesions after radiotherapy. Even so, SBRT is still controversial in the rescue treatment of recurrent lung cancer after radiotherapy, especially for ultral-central lesions close to mediastinal structures (such as bronchus, esophagus and large blood vessels), which have a high probability of fatal side effects. However, a few studies on the application of SBRT in the reirradiation for ultral-central lung cancer have shown acceptable safety and efficacy. Generally speaking, there are few studies on SBRT in the treatment of recurrent ultral-central tumor with limited data. The purpose of this study is to further evaluate the efficacy and toxicities of SBRT in the treatment of recurrent ultral-central tumors after radiotherapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
View:

• Pathological diagnosis is malignant tumor.

• The location of the target lesion belongs to the ultra-central type of chest.

• The target lesion had a history of radiotherapy, and the lesion diameter is ≤ 5cm.

• There is no extensive systemic metastasis or although there is metastasis, the metastasis have been controlled by previous treatment.

• KPS\>70, no serious or uncontrolled underlying diseases, such as severe or uncontrolled hypertension, diabetes, cardiovascular and cerebrovascular diseases and organ dysfunction, and patients are expected to be tolerated by radiotherapy.

Locations
Other Locations
China
Peking University Third Hospital
RECRUITING
Beijing
Contact Information
Primary
Zhe Ji, M.D.
aschoff@163.com
008618710002823
Backup
Junjie Wang, M.D.
junjiewang_edu@sina.cn
008601082265921
Time Frame
Start Date: 2022-05-01
Estimated Completion Date: 2027-04-30
Participants
Target number of participants: 40
Related Therapeutic Areas
Sponsors
Leads: Peking University Third Hospital

This content was sourced from clinicaltrials.gov