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Randomized controlled clinical study of conventional fractionated intensity modulated thoracic radiotherapy and simultaneous integrated boost intensity modulated radiotherapy in patients with limited stage small cell lung cancer

Randomized controlled clinical study of conventional fractionated intensity modulated radiotherapy and simultaneous integrated boost intensity modulated thoracic radiotherapy in patients with limited stage small cell lung cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018084
Enrollment
Unknown
Registered
2018-08-29
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-09-03

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

Conditions

limited stage small cell lung cancer

Interventions

Group 1:conventional fractionated intensity modulated radiotherapy (IMRT)
Group 2:simultaneous integrated boost intensity modulated radiotherapy

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Histological diagnosed limited stage small cell lung cancer; 2. ECOG 0-1; 3. Life expectancy>6 months; 4. Age=18; 5. No radiation history; 6.No severe complications, such as hypertension, coronary heart disease or mental illness, no history of severe allergies. 7. HGB=90 g/L,WBC=3.0×10^9/L,ANC=1.5×10^9/L,PLT=50×10^9/L,SCr=1.5 ×ULN,TBIL=1.5×ULN, AST and ALT=1.5×ULN; 8. Subjects were willing to join in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: Patients with any of the following may not be included in this study: 1. The patient has (a history of) other malignant tumors, but has been cured except cervical carcinoma in situ,non melanoma skin cancer and superficial bladder tumor in the past five years; 2. Pregnant or lactating patients; 3. 4 weeks prior to the start of the study involved in other clinical trial; 4. A history of immune deficiency, or has other acquired, congenital immunodeficiency disease, or a history of organ transplantation; 5. According to the researcher's judgment, there are serious diseases that endanger the patient's safety or influence the clinical research; 6. The time from the first chest radiotherapy to the first chemotherapy was more than 60 days; 7. The researchers asked for the quitting of enrollment.

Design outcomes

Primary

MeasureTime frame
Thoracic local control rate;Thoracic PFS;PFS;

Secondary

MeasureTime frame
OS;Incidence of radiation pneumonia;Incidence of radiation esophagitis;

Countries

China

Contacts

Public ContactLihua Dong

The First Hospital of Jilin University

drlhdong@163.com+86 15843073216

Outcome results

None listed

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