This trial is active, not recruiting.

Condition malignant pleural mesothelioma
Treatments extrapleural pneumonectomy (epp), pleurectomy/decortication, cisplatin, gemcitabine, amifostine, sodium thiosulfate
Phase phase 1
Sponsor Brigham and Women's Hospital
Collaborator Dana-Farber Cancer Institute
Start date November 2007
End date November 2011
Trial size 36 participants
Trial identifier NCT00571298, 07-091


RATIONALE: After removal of visible cancer in the chest, chemotherapy drugs are used to kill or stop tumor cells from dividing, so that they stop growing or/and die. Cisplatin is currently used safely as in intra-operative treatment for malignant pleural mesothelioma. This study is aimed to determine if the addition of gemcitabine as a second intracavitary chemotherapy can be accomplished safely.

PURPOSE: This is a Phase I trial to study the efficacy of combination chemotherapy consisting of gemcitabine and 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 and the effect of cytoprotection agents: amifostine and sodium thiosulfate to counteract potential side effects of chemotherapy.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification safety study
Intervention model single group assignment
Masking open label
Primary purpose treatment

Primary Outcomes

To establish the maximally tolerated dose (MTD) of intraoperative Intrathoracic/Intraperitoneal hyperthermic gemcitabine and cisplatin combination modulated by amifostine and sodium thiosulfate in patients with malignant pleural mesothelioma.
time frame: 2 years

Secondary Outcomes

To determine and quantitate the safety of this combination in these patients by defining the dose limiting toxicity.
time frame: 2 years
To study the pharmacokinetics of gemcitabine and cisplatin combination administered in this way.
time frame: 2 years

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - Histologically-proven diagnosis of stages I to III malignant mesothelioma of the pleura and negative mediastinal N2 lymph nodes (Malignancy is confined to the affected hemithorax) - Adequate organ function including the following: adequate cardiac function, pulmonary function, renal and hepatic function and bone marrow reserve - Adequate overall physical activity - Surgical candidate for cytoreductive surgery Exclusion Criteria: - Extended disease outside the ipsilateral hemithorax as proven histologically, radiologically and/or intraoperatively - Have received chemotherapy and or radiation therapy within the last 3 years at the time of study entry - Serious concomitant systemic disorders - Second active primary malignancy (to exclude non- melanoma skin cancer) - Pregnancy at the time of the operation - Psychiatric or addictive disorder which would preclude obtaining informed consent

Additional Information

Official title A Phase I Trial of Extrapleural Pneumonectomy/Pleurectomy Decortication, Intrathoracic/Intraperitoneal Hyperthermic (IOHC) Cisplatin and Gemcitabine With Intravenous Amifostine and Sodium Thiosulfate Cytoprotection for Patients With Resectable Malignant Pleural Mesothelioma
Principal investigator David J Sugarbaker, MD
Description - This is a dose escalation study of gemcitabine with a fixed dose of cisplatin - Patients will undergo cytoreductive surgery, which entails the removal of the inner and outer lining of the lung (pleurectomy/decortication) with or without the lung itself (extrapleural pneumonectomy), including the lining overlying the pericardium and diaphragm. Resection of the pericardium and diaphragm are occasionally necessary to remove all visable tumor. This surgery is part of standard care for malignant pleural mesothelioma. - After surgery, a one hour lavage with heated cisplatin and or gemcitabine will be administered to the hemithorax (and abdominal regions if the diaphragm is no longer present). - Patients will remain hospitalized until they have recovered from surgery (usually 7-14 days). - Patients will return to the hospital during the first month after their surgery to be evaluated by the medical staff. - Dose escalation: 1) Three patients will be treated at the first dose level of gemcitabine. Labs will be monitored on a weekly basis, including a CBC, Chem-7, and LFT's. In the absence of developing dose-limiting toxicity (DLT) among the first 3 patients treated, dosages can be escalated. DLT will be defined as any grade 3 or higher renal toxicity, thrombocytopenia or other grade 3 toxicity not related to surgery 2) If none of these 3 patients have any toxicity, we will proceed to the next level of gemcitabine. 3) If DLT occurs in 1 of 3 patients at a given dose level, then 3 additional patients are added at that dose (for a total of 6 at this level)If no DLT occurs, we will proceed to the next level of gemcitabine. If DLT occurs in another patient, this dose is considered the maximum tolerated dose (MTD). 4) At any dose, 3 cases of DLT lead to discontinuation of recruitment at that dose and enrollment of 3 additional patients at a lower dose.
Trial information was received from ClinicalTrials.gov and was last updated in September 2014.
Information provided to ClinicalTrials.gov by Dana-Farber Cancer Institute.