Skip to content

Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost in brain metastases for non small cell lung cancer

A randomised controlled trial about Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost in symptomatic brain metastases for non small cell lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013204
Enrollment
Unknown
Registered
2017-11-01
Start date
2013-01-01
Completion date
Unknown
Last updated
2017-11-06

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

Conditions

non small cell lung cancer

Interventions

Two groups:different whole brain dose of Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost (SIB-IMRT)

Sponsors

Taizhou Hospital of Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. a histopathologically or cytologically proven non-small cell lung cancer(NSCLC) and an axial gadolinium-enhanced T1 sequence magnetic resonance scan(MRI) confirmed brain metastases(BMs) and symptomatic brain metastases. 2. have an estimated survival of at least 4 weeks; 3. Karnofsky Performance Status Scale (KPS) of 60-100; 4. Patients laboratory values had to meet these restrictions: hemoglobin>100g/L, platelets>70*10^9/L, white blood cells>4*10^9/L; 5. sign the consent form.;Inclusion criteria: 1. a histopathologically or cytologically proven non-small cell lung cancer(NSCLC) and an axial gadolinium-enhanced T1 sequence magnetic resonance scan(MRI) confirmed brain metastases(BMs) and symptomatic brain metastases. 2. have an estimated survival of at least 4 weeks; 3. Karnofsky Performance Status Scale (KPS) of 60-100; 4. Patients laboratory values had to meet these restrictions: hemoglobin>100g/L, platelets>70*10^9/L, white blood cells>4*10^9/L; 5. sign the consent form.;Inclusion criteria: 1. a histopathologically or cytologically proven non-small cell lung cancer(NSCLC) and an axial gadolinium-enhanced T1 sequence magnetic resonance scan(MRI) confirmed brain metastases(BMs) and symptomatic brain metastases. 2. have an estimated survival of at least 4 weeks; 3. Karnofsky Performance Status Scale (KPS) of 60-100; 4. Patients laboratory values had to meet these restrictions: hemoglobin>100g/L, platelets>70*10^9/L, white blood cells>4*10^9/L; 5. sign the consent form.;Inclusion criteria: 1. a histopathologically or cytologically proven non-small cell lung cancer(NSCLC) and an axial gadolinium-enhanced T1 sequence magnetic resonance scan(MRI) confirmed brain metastases(BMs) and symptomatic brain metastases. 2. have an estimated survival of at least 4 weeks; 3. Karnofsky Performance Status Scale (KPS) of 60-100; 4. Patients laboratory values had to meet these restrictions: hemoglobin>100g/L, platelets>70*10^9/L, white blood cells>4*10^9/L; 5. sign the consent form.;Inclusion criteria: 1. a histopathologically or cytologically proven non-small cell lung cancer(NSCLC) and an axial gadolinium-enhanced T1 sequence magnetic resonance scan(MRI) confirmed brain metastases(BMs) and symptomatic brain metastases. 2. have an estimated survival of at least 4 weeks; 3. Karnofsky Performance Status Scale (KPS) of 60-100; 4. Patients laboratory values had to meet these restrictions: hemoglobin>100g/L, platelets>70*10^9/L, white blood cells>4*10^9/L; 5. sign the consent form.

Exclusion criteria

Exclusion criteria: 1. patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy; 2. patients who had received previous brain irradiation; 3. Patients laboratory values could not match the inclusion criteria; 4. could not be regularly followed; 5. with leptomeningeal involvement.;Exclusion criteria: 1. patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy; 2. patients who had received previous brain irradiation; 3. Patients laboratory values could not match the inclusion criteria; 4. could not be regularly followed; 5. with leptomeningeal involvement.;Exclusion criteria: 1. patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy; 2. patients who had received previous brain irradiation; 3. Patients laboratory values could not match the inclusion criteria; 4. could not be regularly followed; 5. with leptomeningeal involvement.;Exclusion criteria: 1. patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy; 2. patients who had received previous brain irradiation; 3. Patients laboratory values could not match the inclusion criteria; 4. could not be regularly followed; 5. with leptomeningeal involvement.;Exclusion criteria: 1. patients had major medical illnesses or psychiatric impairments which will prevent completion of the protocol therapy; 2. patients who had received previous brain irradiation; 3. Patients laboratory values could not match the inclusion criteria; 4. could not be regularly followed; 5. with leptomeningeal involvement.

Design outcomes

Primary

MeasureTime frame
magnetic resonance image;

Countries

China

Contacts

Public ContactHaihua Yang;Haihua Yang;Haihua Yang;Haihua Yang;Haihua Yang ;;;;

Taizhou Hospital of Zhejiang Province;Taizhou Hospital of Zhejiang Province;Taizhou Hospital of Zhejiang Province;Taizhou Hospital of Zhejiang Province;Taizhou Hospital of Zhejiang Province

yhh93181@hotmail.com;yhh93181@hotmail.com;yhh93181@hotmail.com;yhh93181@hotmail.com;yhh93181@hotmail.com+86 13819639006;+86 13819639006;+86 13819639006;+86 13819639006;+86 13819639006

Outcome results

None listed

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