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Simultaneous integrated boost hyperfrfrated radiotherapy versus standard-dose radiotherapy for patients with limited stage small-cell lung cancer: a randomized controlled trial

Simultaneous integrated boost hyperfrfrated radiotherapy versus standard-dose radiotherapy for patients with limited stage small-cell lung cancer: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056627
Enrollment
Unknown
Registered
2022-02-09
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-09-04

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

Test group:51Gy/30F/bid
Control Group:45Gy/30F/bid

Sponsors

Gansu Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Small cell lung cancer confirmed by histology or cytology; According to the stage of American veterans, it is limited stage small cell lung cancer; 2. Age: 18-85 years; 3. ECOG score: 0 – 2 points; 4. The function of main organs can ensure the smooth completion of treatment, that is, meet the following standards: Hemoglobin (Hb) = 90g/L; Absolute neutrophil count (ANC) = 1.5 × 109/L Platelet (PLT) = 100 × 109/L White blood cell (WBC) = 3.0 × 109/L Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) = 3 × ULN Total serum bilirubin (TBIL) = 1.5 × ULN Serum creatinine (Cr) = 1.5 × ULN or creatinine clearance = 5; ml/min 5. Lung function can tolerate radiotherapy; 6. No other malignant tumors except small cell lung cancer were confirmed; 7. Volunteer to join the study, sign the informed consent form, and have good compliance.

Exclusion criteria

Exclusion criteria: 1.Previous radiotherapy to the thorax; 2.Pregnancy or lactating women; 3.No serious concomitant systemic disorders (for example active infection, unstable cardiovascular disease) that in the opinion of the investigator would compromise the patients ability to complete the study or interfere with the evaluation of the efficacy and safety of the study treatment.

Design outcomes

Primary

MeasureTime frame
2 year OS;

Secondary

MeasureTime frame
PFS;Median overall survival;Local control rate;Adverse reactions;

Countries

China

Contacts

Public ContactShao Lihua

Gansu Provincial Cancer Hospital

1558163727@qq.com+86 18054162294

Outcome results

None listed

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