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Image-guided Stereotactic Body Radiotherapy and Surgical Treatment for Stage I Non-small Cell lungCcancer by Comparative Effectiveness Research

Image-guided Stereotactic Body Radiotherapy and Surgical Treatment for Stage I Non-small Cell lungCcancer by Comparative Effectiveness Research

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-15006864
Enrollment
Unknown
Registered
2015-08-01
Start date
2015-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Stage I Non-small Cell lungCcancer

Interventions

Experimental group:Stereotactic Body Radiotherapy
The control group:Surgery

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients were required to be >=18 years old, with an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 and weight loss 50% predicted; 6. Willing and able to comply the protocol and attend all study visits, provide written informed consent prior to the initiation of any study-related procedures; 7. WOCBP using and willing to continue to use adequate contraceptive precautions for the duration of the study.

Exclusion criteria

Exclusion criteria: 1. Patients with any component of small cell lung carcinoma; 2. Patients with evidence of a malignant pleural or pericardial effusion or patients with T4 disease with radiographic evidence of massage invasion of a large pulmonary artery and tumor causing significant narrowing and destruction of that artery; 3. Who received previous thoracic radiotherapy, previous surgery, previous chemotherapy with bleomycin, regular use of supplemental oxygen; 4. Pregnancy or lactation or who plan to pregnant; 5. Who have oher malignancies (with the expection of cases of cervical carcinoma in situ or non-malignant melanoma skin cancer that had been clinically cured for at least 5 years); 6. Severe, active co-morbidity, such as human immunodeficiency virus,acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration, hepatic insufficiency resulting in clinical jaundice and/or coagulation defects, chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration, poorly controlled diabetes; 7. Patients who are participating in a concurrent treatment protocol; 8. The subject may not the study because of other study, or researchers think are unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
Overall survival rate;Progress control of local rate;

Countries

China

Contacts

Public ContactHeJian
hejian62@163.com+86 13386057161

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026