Mesothelioma Related Clinical Trials:
Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin and Intravenous Sodium Thiosulfate in the Multimodality Treatment of Malignant Pleural Mesothelioma
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Status: Active
Sponsors and Collaborators: Dana-Farber Cancer Institute, Brigham and Women's Hospital
Information provided by: Dana-Farber Cancer Institute
Government Identifier: NCT00165555
Condition: Pleural Mesothelioma, Malignant Pleural Mesothelioma
Intervention: Drug: Cisplatin; Drug: Sodium Thiosulfate
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Purpose:
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.
| Study Type: |
Interventional |
| Study Design: |
Treatment, Non-Randomized, Open Label, Dose Comparison, Single Group Assignment, Safety Study |
|
| Official Title: |
Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin and Intravenous Sodium Thiosulfate in the Multimodality Treatment of Malignant Pleural Mesothelioma |
Further study details as provided by Dana-Farber Cancer Institute:
Primary Outcome Measures:
- To determine the maximally tolerated dose of intracavitary cisplatin in patients with malignant pleural mesothelioma, [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
- To quantitate the safety of intraoperative intrathoracic/intraperitoneal hyperthermic cisplatin [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]
- to study the pharmacokinetics of cisplatin administered in this way. [ Time Frame: 3 years ] [ Designated as safety issue: No ]
| Enrollment: |
70 |
| Study Start Date: |
August 1999 |
| Estimated Study Completion Date: |
April 2009 |
| Primary Completion Date: |
April 2002 (Final data collection date for primary outcome measure) |
Intervention Details:
Drug: Cisplatin
Given as a heated one-hour lavage to the hemithorax after surgery.
Drug: Sodium Thiosulfate
Given intravenously over 6 hours after the cisplatin lavage.
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.
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Eligibility:
| Ages Eligible for Study: |
18 Years and older |
| Genders Eligible for Study: |
Both |
| Accepts Healthy Volunteers: |
No |
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
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Contacts and Locations:
Please refer to this study by its ClinicalTrials.gov identifier: NCT00165555
Locations
|
| United States, Massachusetts |
|
Brigham and Women's Hospital |
|
Boston, Massachusetts, United States, 02115 |
|
Dana-Farber Cancer Institute |
|
Boston, Massachusetts, United States, 02115 |
Sponsors and Collaborators
|
| Dana-Farber Cancer Institute |
|
| Brigham and Women's Hospital |
Investigators
|
| Principal Investigator: |
David J. Sugarbaker, MD |
Brigham and Women's Hospital |
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Additional Information:
| Responsible Party: |
Brigham and Women's Hospital ( David Sugarbaker, MD ) |
| Study ID Numbers: |
99-124 |
| First Received: |
September 12, 2005 |
| Last Updated: |
December 20, 2007 |
| ClinicalTrials.gov Identifier: |
NCT00165555 |
| Health Authority: |
United States: Institutional Review Board |
Keywords provided by Dana-Farber Cancer Institute:
| cisplatin |
| pleurectomy |
| decortication |
| heated cisplatin |
|
Study placed in the following topic categories:
| Cisplatin |
| Sodium thiosulfate |
| Mesothelioma |
| Adenoma |
| Neoplasms, Glandular and Epithelial |
|
Additional relevant MeSH terms:
| Mesothelioma |
| Anti-Infective Agents |
| Neoplasms by Histologic Type |
| Antioxidants |
| Molecular Mechanisms of Pharmacological Action |
| Neoplasms, Mesothelial |
| Antineoplastic Agents |
| Physiological Effects of Drugs |
| Protective Agents |
|
|
| Pharmacologic Actions |
| Anti-Bacterial Agents |
| Neoplasms |
| Radiation-Sensitizing Agents |
| Therapeutic Uses |
| Chelating Agents |
| Antitubercular Agents |
| Antidotes |
|
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