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Feasibility and efficacy of helical tomotherapy for stage III non-small cell lung cancer in comparison with three-dimensional conformal radiotherapy by Comparative Effectiveness Research

Feasibility and efficacy of helical tomotherapy for stage III non-small cell lung cancer in comparison with three-dimensional conformal radiotherapy by Comparative Effectiveness Research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15006871
Enrollment
Unknown
Registered
2015-07-28
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

lung cancer

Interventions

Experimental group:helical tomotherapy
The control group:three-dimensional conformal radiotherapy

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients should be diagnosed as NSCLC histologically or cytologically; 2. CT/PET-CT staging should be stage III (IIIA T4N0-1M0, T3N1M0, T1-3N2M0; IIIB T4N2M0, TxN3M0); 3. Age >=18 years old; 4. KPS scores>=60,the weight loss in last 6 months4.0*10^9/L, absolute neutrophil count>1.5*10^9/L,hemoglobin>110g/L,platelet count>100*10^9/L; liver function: bilirubin of blood cholesterol 1L or FEV1>40% predicted value, DLCO>30%predicted value; 6. The patient has chest CT in recent 4 weeks, the measurable focus, and cranial CT or MRI or FDG-PET before being admitted. CT scan is needed (unless there is contraindication, venous enhancement will be better), including bilateral lung, mediastinum, liver, and adrenal gland; 7. life expectancy >=12 weeks; 8. The size of primary tumor must be measured by CT; 9. no other cancer; 10. patients can understand the situation of the study and has signed informed consent.

Exclusion criteria

Exclusion criteria: 1) obvious neurologic or psychiatric history; such as Alzheimerdisease, which may affect comprehensive ability; 2) Being diagnosed as small cell lung cancer histologically or cytologically; 3) KPS score <50 or PS score is 3-4; 4) Pregnant and lactant women or women with positive pregnancy test; 5) severe comorbidity and complication; 6) Patients who have poor adherence; 7) The patient is confirmed to be regional or distant metastasis with PET exams or postoperative staging; or the patient has primary cancer or precancerous lesion (excluding non-melanomas malignant skin cancer or carcinoma in situ) in past 3 years; 8) Patients who had received radiotherapy because of tumors such as lung cancer, breast cancer and lymphoma will have higher risk of SBRT, because their previous target volumes may coincide with SBRT; 9) Pure bronchioalveolar carcinoma; 10) Active systemic infection or lung, pericardium infection; 11) The patient who has history chemotherapy or has pulmonary resection or pneumonectomy.

Design outcomes

Primary

MeasureTime frame
Overall Survival rate;Local control rate;

Countries

China

Contacts

Public ContactHe Jian
hejian62@163.com+86 13386057161

Outcome results

None listed

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