| September 12, 2005 |
| October 30, 2009 |
| August 1999 |
| April 2002 (final data collection date for primary outcome measure) |
| To determine the maximally tolerated dose of intracavitary cisplatin in patients with malignant pleural mesothelioma, [ Time Frame: 3 years ] [ Designated as safety issue: Yes ] |
| To determine the maximally tolerated dose of intracavitary cisplatin in patients with malignant pleural mesothelioma, |
| Complete list of historical versions of study NCT00165555 on ClinicalTrials.gov Archive Site |
- 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 ]
|
- To quantitate the safety of intraoperative intrathoracic/intraperitoneal hyperthermic cisplatin
- to study the pharmacokinetics of cisplatin administered in this way.
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| |
| Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin for Malignant Pleural Mesothelioma |
| Pleurectomy/Decortication Followed by Intrathoracic/Intraperitoneal Heated Cisplatin and Intravenous Sodium Thiosulfate in the Multimodality Treatment of Malignant Pleural Mesothelioma |
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. |
- 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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| Phase I |
| Interventional |
| Treatment, Non-Randomized, Open Label, Dose Comparison, Single Group Assignment, Safety Study |
- Pleural Mesothelioma
- Malignant Pleural Mesothelioma
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- Drug: Cisplatin
- Drug: Sodium Thiosulfate
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| |
| |
| |
| Active, not recruiting |
| 70 |
| April 2010 |
| April 2002 (final data collection date for primary outcome measure) |
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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| Both |
| 18 Years and older |
| No |
| Contact information is only displayed when the study is recruiting subjects |
| United States |
| |
| NCT00165555 |
| David Sugarbaker, MD, Brigham and Women's Hospital |
| 99-124 |
| Dana-Farber Cancer Institute |
| Brigham and Women's Hospital |
| Principal Investigator: |
David J. Sugarbaker, MD |
Brigham and Women's Hospital |
|
|
| Dana-Farber Cancer Institute |
| October 2009 |