Palliative 3-Dimensional Conformal Radiation Therapy in Reducing Radiation Side Effects in Patients With Lung Cancer. ICORG 06-34
- Conditions
- Lung Cancer
- Interventions
- Other: questionnaire administrationProcedure: quality-of-life assessmentRadiation: 3-dimensional conformal radiation therapyRadiation: palliative radiation therapyRadiation: whole-brain radiation therapy
- Registration Number
- NCT01176487
- Lead Sponsor
- Cancer Trials Ireland
- Brief Summary
RATIONALE: 3-dimensional conformal radiation therapy may lessen side effects caused by palliative radiation therapy and improve the quality of life of patients with lung cancer.
PURPOSE: This clinical trial is studying how well 3-dimensional conformal radiation therapy works in reducing the side effects of palliative radiation in patients with lung cancer.
- Detailed Description
The primary purpose of this study is to demonstrate that using technically sophisticated 3-dimensional conformal radiation therapy for the palliative treatment of lung cancer patients will result in equivalent degrees of symptom relief and a reduction in the primary endpoint of oesophagitis.
Single arm therapeutic clinical study.
RT Treatment Regimens:
17 Gy/2 fractions or 20Gy/5 fractions or 39Gy/13 fractions
Primary Endpoint:
-The occurrence of Grade 3 or higher oesophagitis in the interval between start and 1-month post completion of treatment as determined by CTCAE Version 4.02
Patients will be assessed pre treatment, during treatment, 2 weeks post completion of treatment, one month post completion of treatment, three months post completion of treatment, and three monthly thereafter
-All patients who complete treatment (and whose on-treatment toxicity is documented) will be evaluable.
Secondary Endpoint:
* Quality of Life Assessment. All patients will be required to complete the EORTC QLQ-C15-PAL (Version 1) and the Lung Specific Module (LC 13)
* The occurrence of other AEs
Safety Endpoint:
-Radio-induced oesophagitis, acute and long term, using the CTCAE Version 4.02.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Age > 18 years
- Karnofsky Performance Status of > or equal to 40%
- Patients with locally advanced or metastatic small cell or non-small cell lung cancer
- The presence of intra-thoracic symptoms requiring palliative treatment
- WBI (if required) is permitted
- The patient's condition must permit waiting for the 3-dimensional design process to be implemented. This will be at the discretion of the Consultant Physician
- Patients presenting with pleural effusions - provided the pleural effusion does not prevent the reasonably accurate delineation of the target volume
- Intra-thoracic disease requiring palliation must be clearly evident on a diagnostic CT scan
- Life expectancy of at least 3 months (assessed by clinician)
- Provision of written informed consent in line with ICH-GCP guidelines
-In the opinion of the Investigator, any evidence of severe or uncontrolled systematic disease (e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description A whole-brain radiation therapy A clinical trial using 3-dimensional conformal radiation therapy to reduce the toxicity of palliative radiation for lung cancer A palliative radiation therapy A clinical trial using 3-dimensional conformal radiation therapy to reduce the toxicity of palliative radiation for lung cancer A questionnaire administration A clinical trial using 3-dimensional conformal radiation therapy to reduce the toxicity of palliative radiation for lung cancer A quality-of-life assessment A clinical trial using 3-dimensional conformal radiation therapy to reduce the toxicity of palliative radiation for lung cancer A 3-dimensional conformal radiation therapy A clinical trial using 3-dimensional conformal radiation therapy to reduce the toxicity of palliative radiation for lung cancer
- Primary Outcome Measures
Name Time Method Occurrence of esophagitis grade 3 or higher according to CTCAE Version 4.02 2015 Quality of life as assessed using the EORTC QLQ-C15-PAL (Version 1) questionnaire and the Lung Specific Module (LC 13) 2015
- Secondary Outcome Measures
Name Time Method Local intra-thoracic symptoms 2015
Trial Locations
- Locations (2)
St Luke's Radiation Oncology Network (SLRON)
🇮🇪Dublin, Ireland
Galway University Hospital
🇮🇪Galway, Ireland