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Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin for Malignant Pleural Mesothelioma

Primary Purpose

Pleural Mesothelioma, Malignant Pleural Mesothelioma

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Cisplatin
Sodium Thiosulfate
Sponsored by
Dana-Farber Cancer Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pleural Mesothelioma focused on measuring cisplatin, pleurectomy, decortication, heated cisplatin

Eligibility Criteria

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

Inclusion Criteria: Histopathologic confirmation of malignant pleural mesothelioma Patients who are able to tolerate surgical cytoreduction but unable to undergo extrapleural pneumonectomy due to poor cardiopulmonary reserve or tumor invasion 18 years of age or older Malignancy is confined to the affected hemithorax. Grossly normal cardiac function with an EKG showing no cardiomyopathy or acute changes Evidence of adequate renal and hepatic function Karnofsky performance status of 70% or greater Exclusion Criteria: Extended disease outside the ipsilateral hemithorax as determined radiologically and intraoperatively Distant metastases Non-malignant systemic disease Active concomitant malignancy Psychiatric or addictive disorders which would preclude obtaining informed consent Prior treatment within the last 2 months, other than surgical resection for their current malignancy

Sites / Locations

  • Brigham and Women's Hospital
  • Dana-Farber Cancer Institute

Outcomes

Primary Outcome Measures

To determine the maximally tolerated dose of intracavitary cisplatin in patients with malignant pleural mesothelioma,

Secondary Outcome Measures

To quantitate the safety of intraoperative intrathoracic/intraperitoneal hyperthermic cisplatin
to study the pharmacokinetics of cisplatin administered in this way.

Full Information

First Posted
September 12, 2005
Last Updated
March 26, 2014
Sponsor
Dana-Farber Cancer Institute
Collaborators
Brigham and Women's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00165555
Brief Title
Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin for Malignant Pleural Mesothelioma
Official Title
Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin and Intravenous Sodium Thiosulfate in the Multimodality Treatment of Malignant Pleural Mesothelioma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
August 1999 (undefined)
Primary Completion Date
April 2002 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Dana-Farber Cancer Institute
Collaborators
Brigham and Women's Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study it to determine the safety and maximally tolerated dose (MTD) of cisplatin administered in the operating room and put into the chest and abdomen for one hour. We are also looking at the effects of heating the chemotherapy to a temperature of 42 degrees celsius.
Detailed Description
Patients will undergo surgery with pleurectomy/decortication which entails the removal of the inner and outer skin of the lung, including the pleura overlying the pericardium and diaphragm. Resection of the pericardium and diaphragm are occasionally necessary to debulk the tumor. This surgery is part of standard care for pleural mesothelioma. After surgery, a one hour lavage with heated cisplatin will be administered to the hemithorax (and abdominal regions if the diaphragm is no longer present). The lung itself is not removed, only the diseased portion of the lung and surrounding areas with tumor. Immediately following the one-hour lavage, a six hour infusion of sodium thiosulfate will begin to help reduce the side effects of the cisplatin. Patients will remain hospitalized until they have recovered from surgery (usually 7-14 days). Patients will return to the hospital three months after their surgery to have fluid drawn from their chest via an ultrasound guided thoracentesis. This is called a saline wash. Patients will be in the study actively for three months. This includes a 2-week and 4-week post-operative follow-up in which blood work is performed. As well as a 3-month follow-up for the saline wash. Long-term follow-up includes computed tomography of the chest and abdomen every 6 months to assess recurrence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pleural Mesothelioma, Malignant Pleural Mesothelioma
Keywords
cisplatin, pleurectomy, decortication, heated cisplatin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Cisplatin
Intervention Description
Given as a heated one-hour lavage to the hemithorax after surgery.
Intervention Type
Drug
Intervention Name(s)
Sodium Thiosulfate
Intervention Description
Given intravenously over 6 hours after the cisplatin lavage.
Primary Outcome Measure Information:
Title
To determine the maximally tolerated dose of intracavitary cisplatin in patients with malignant pleural mesothelioma,
Time Frame
3 years
Secondary Outcome Measure Information:
Title
To quantitate the safety of intraoperative intrathoracic/intraperitoneal hyperthermic cisplatin
Time Frame
3 years
Title
to study the pharmacokinetics of cisplatin administered in this way.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histopathologic confirmation of malignant pleural mesothelioma Patients who are able to tolerate surgical cytoreduction but unable to undergo extrapleural pneumonectomy due to poor cardiopulmonary reserve or tumor invasion 18 years of age or older Malignancy is confined to the affected hemithorax. Grossly normal cardiac function with an EKG showing no cardiomyopathy or acute changes Evidence of adequate renal and hepatic function Karnofsky performance status of 70% or greater Exclusion Criteria: Extended disease outside the ipsilateral hemithorax as determined radiologically and intraoperatively Distant metastases Non-malignant systemic disease Active concomitant malignancy Psychiatric or addictive disorders which would preclude obtaining informed consent Prior treatment within the last 2 months, other than surgical resection for their current malignancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David J. Sugarbaker, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Dana-Farber Cancer Institute
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin for Malignant Pleural Mesothelioma

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