RATIONALE: Video-assisted surgery to remove part of the tissue layer covering the inside of the chest cavity may be effective in treating pleural effusion and cause less damage to normal tissue. Talc pleurodesis may keep fluid from building up in the chest cavity. It is not yet known which therapy is more effective in treating pleural effusion caused by malignant mesothelioma. PURPOSE: This randomized phase III trial is studying video-assisted surgery to see how well it works compared with talc pleurodesis in treating patients with malignant mesothelioma.
OBJECTIVES: Primary * Compare the effectiveness of video-assisted thoracoscopic cytoreductive pleurectomy vs talc pleurodesis, in terms of 1-year survival, in patients with suspected or proven malignant mesothelioma. Secondary * Compare the control of pleural effusion in these patients. * Compare procedure-related complications in these patients. * Compare the symptoms and quality of life of these patients at 3, 6, and 12 months after treatment. * Compare the length of hospital stay for these patients. * Compare the exercise tolerance of these patients at 3, 6, and 12 months after treatment. * Determine the cost to the health service, in terms of resources used for procedures, hospital bed usage, and cost of primary and secondary care over 12 months. OUTLINE: This is a multicenter study. Patients are stratified according to risk (high vs low). Patients are randomized to 1 of 2 treatment arms. * Arm I (video-assisted thoracoscopic \[VAT\] cytoreductive pleurectomy): Patients undergo VAT cytoreductive pleurectomy either at the time of biopsy or after confirmation of biopsy results. * Arm II (talc pleurodesis): Patients undergo talc pleurodesis via an indwelling intercostal chest drain or via thoracoscopy either at the time of biopsy or after confirmation of biopsy results. Quality of life, complications, and resource use are assessed at baseline and at 1, 3, 6, and 12 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
196
Talc pleurodesis
Talc pleurodesis via thoracoscopy
Video-assisted thoracoscopic pleurectomy
Basildon University Hospital
Basildon, England, United Kingdom
Papworth Hospital
Cambridge, England, United Kingdom
Glenfield Hospital
Leicester, England, United Kingdom
Guy's Hospital
London, England, United Kingdom
Royal Hallamshire Hospital
Sheffield, England, United Kingdom
Survival at 1 year after treatment
Time frame: 1 year
Control of pleural effusion
Time frame: 1 year
Complications, including need for more surgery, persistent air leak requiring pleural intubation for > 10 days, and hospital stay for > 12 days
Time frame: 1 year
Symptoms and quality of life as assessed by the EuroQol questionnaire
Time frame: 0, 1, 3, 6 12 months
Length of hospital stay
Time frame: 1 year
Exercise tolerance
Time frame: 0, 1, 3, 6 12 months
Cost to the health service, in terms of resources used for procedures, hospital bed usage, and cost of primary and secondary care over 12 months
Time frame: 0, 1, 3, 6 12 months
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