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Standard Chest Tube Compared With a Small Catheter in Treating Malignant Pleural Effusion in Patients With Cancer

Primary Purpose

Metastatic Cancer, Pulmonary Complications

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
talc
dyspnea management
Sponsored by
Alliance for Clinical Trials in Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Cancer focused on measuring malignant pleural effusion, pulmonary complications

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Radiologic evidence of a unilateral malignant pleural effusion requiring sclerosis or ongoing drainage because it is symptomatic (dyspnea and/or progressive fatigue) An asymptomatic patient is eligible if the patient underwent a prior thoracentesis within the past 2 weeks and was symptomatic before the procedure No bilateral effusions by plain chest x-ray Histologically or cytologically confirmed solid tumor or hematologic malignancy Histologic confirmation of malignant cells in pleural fluid is not required Pleural spaces must be naive to pleurodesis attempts No prior intrapleural therapy (defined as a chest tube in place or placed to drain an effusion, prior surgical pleurectomy, or any prior chemical or mechanical pleurodesis on the ipsilateral side) Placement of a small interventional radiology catheter for temporary drainage is not considered intrapleural therapy as long as no sclerosant medication was given and it has not been in place longer than 10 days PATIENT CHARACTERISTICS: Age 18 and over Performance status CTC 0-2 Hematopoietic Granulocyte count at least 1,500/mm^3 Platelet count at least 100,000/mm^3 Pulmonary No active pleural infection Other No allergy to talc No surgical contraindication to talc usage Not pregnant or nursing Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Chemotherapy Concurrent systemic chemotherapy allowed Radiotherapy Concurrent palliative radiotherapy to a symptomatic lesion allowed except to the treated hemithorax within 30 days of the drainage procedure Surgery See Disease Characteristics Prior thoracotomies without specific pleural ablation (including lobectomy but not pneumonectomy) allowed Prior needle-based diagnostic interventions (fine-needle aspiration, small bore catheter drainage of less than 10 days, or thoracentesis) allowed

Sites / Locations

  • Providence Saint Joseph Medical Center - Burbank

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Arm I

Arm II

Arm Description

Patients undergo placement of a standard pleural chest tube. Within 36 hours of chest tube placement, patients undergo pleurodesis comprising intrapleural administration of talc slurry once followed by clamping of the chest tube for 2 hours while different patient positions are used to distribute the talc. The chest tube is then unclamped to allow continuous drainage. When the chest tube drainage is less than 150 mL over 24 hours, pleurodesis is assumed and the chest tube is removed.

Patients undergo pleurodesis comprising placement of a small (PleurX) catheter followed by pleural drainage for up to 90 minutes once daily. When the catheter drainage is less than 30 mL per day for 3 consecutive days, pleurodesis is assumed and the catheter is removed.

Outcomes

Primary Outcome Measures

Effusion control

Secondary Outcome Measures

Quality of Life

Full Information

First Posted
August 5, 2002
Last Updated
July 1, 2016
Sponsor
Alliance for Clinical Trials in Oncology
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00042770
Brief Title
Standard Chest Tube Compared With a Small Catheter in Treating Malignant Pleural Effusion in Patients With Cancer
Official Title
Phase III Comparison of Catheter Based Therapy of Pleural Effusions in Cancer Patients (Optimal Pleural Effusion Control, OPEC)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
May 2002 (undefined)
Primary Completion Date
February 2005 (Actual)
Study Completion Date
February 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Alliance for Clinical Trials in Oncology
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: It is not yet known whether pleurodesis using a chest tube with infusions of talc is more effective in improving quality of life than pleurodesis using a small catheter in treating malignant pleural effusion. PURPOSE: Randomized phase III trial to compare the effectiveness of a chest tube and talc with that of a small catheter in treating malignant pleural effusion in patients who have cancer.
Detailed Description
OBJECTIVES: Compare the success rate in patients with cancer who undergo pleurodesis using a standard chest tube with talc slurry vs a small (PleurX) catheter for the treatment of a symptomatic unilateral malignant pleural effusion. Compare the 30-day effusion control rate in patients treated with these procedures. Compare quality of life in these patients at 7-14 and 30-37 days after treatment with these procedures. Compare patient acceptance and satisfaction after treatment with these procedures. Compare the level of symptoms and dyspnea experienced by patients treated with these procedures. Compare the types, causes, and rates of early technical failures of these procedures in these patients. Compare the 30-day effusion recurrences in patients treated with these procedures. Compare the 60-day durability of pleurodesis in patients treated with these procedures. Compare the mortality, morbidity, and common surgical complications in patients treated with these procedures. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to inpatient status (yes vs no), disease type (breast vs lung vs other), and concurrent systemic chemotherapy (yes vs no). Patients are randomized to 1 of 2 treatment arms. Arm I: Patients undergo placement of a standard pleural chest tube. Within 36 hours of chest tube placement, patients undergo pleurodesis comprising intrapleural administration of talc slurry once followed by clamping of the chest tube for 2 hours while different patient positions are used to distribute the talc. The chest tube is then unclamped to allow continuous drainage. When the chest tube drainage is less than 150 mL over 24 hours, pleurodesis is assumed and the chest tube is removed. Arm II: Patients undergo pleurodesis comprising placement of a small (PleurX) catheter followed by pleural drainage for up to 90 minutes once daily. When the catheter drainage is less than 30 mL per day for 3 consecutive days, pleurodesis is assumed and the catheter is removed. Quality of life and dyspnea are assessed at baseline and then at 7-14 and 30-37 days after treatment. Patients are followed at 30 and 60 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Cancer, Pulmonary Complications
Keywords
malignant pleural effusion, pulmonary complications

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
67 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm I
Arm Type
Active Comparator
Arm Description
Patients undergo placement of a standard pleural chest tube. Within 36 hours of chest tube placement, patients undergo pleurodesis comprising intrapleural administration of talc slurry once followed by clamping of the chest tube for 2 hours while different patient positions are used to distribute the talc. The chest tube is then unclamped to allow continuous drainage. When the chest tube drainage is less than 150 mL over 24 hours, pleurodesis is assumed and the chest tube is removed.
Arm Title
Arm II
Arm Type
Experimental
Arm Description
Patients undergo pleurodesis comprising placement of a small (PleurX) catheter followed by pleural drainage for up to 90 minutes once daily. When the catheter drainage is less than 30 mL per day for 3 consecutive days, pleurodesis is assumed and the catheter is removed.
Intervention Type
Other
Intervention Name(s)
talc
Intervention Description
Given intrapleurally
Intervention Type
Procedure
Intervention Name(s)
dyspnea management
Intervention Description
No talc
Primary Outcome Measure Information:
Title
Effusion control
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Quality of Life
Time Frame
7-14 days and 30-37 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Radiologic evidence of a unilateral malignant pleural effusion requiring sclerosis or ongoing drainage because it is symptomatic (dyspnea and/or progressive fatigue) An asymptomatic patient is eligible if the patient underwent a prior thoracentesis within the past 2 weeks and was symptomatic before the procedure No bilateral effusions by plain chest x-ray Histologically or cytologically confirmed solid tumor or hematologic malignancy Histologic confirmation of malignant cells in pleural fluid is not required Pleural spaces must be naive to pleurodesis attempts No prior intrapleural therapy (defined as a chest tube in place or placed to drain an effusion, prior surgical pleurectomy, or any prior chemical or mechanical pleurodesis on the ipsilateral side) Placement of a small interventional radiology catheter for temporary drainage is not considered intrapleural therapy as long as no sclerosant medication was given and it has not been in place longer than 10 days PATIENT CHARACTERISTICS: Age 18 and over Performance status CTC 0-2 Hematopoietic Granulocyte count at least 1,500/mm^3 Platelet count at least 100,000/mm^3 Pulmonary No active pleural infection Other No allergy to talc No surgical contraindication to talc usage Not pregnant or nursing Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Chemotherapy Concurrent systemic chemotherapy allowed Radiotherapy Concurrent palliative radiotherapy to a symptomatic lesion allowed except to the treated hemithorax within 30 days of the drainage procedure Surgery See Disease Characteristics Prior thoracotomies without specific pleural ablation (including lobectomy but not pneumonectomy) allowed Prior needle-based diagnostic interventions (fine-needle aspiration, small bore catheter drainage of less than 10 days, or thoracentesis) allowed
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Todd Demmy, MD
Organizational Affiliation
Roswell Park Cancer Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Providence Saint Joseph Medical Center - Burbank
City
Burbank
State/Province
California
ZIP/Postal Code
91505
Country
United States

12. IPD Sharing Statement

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Standard Chest Tube Compared With a Small Catheter in Treating Malignant Pleural Effusion in Patients With Cancer

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