NCT Number: NCT00020007
Paclitaxel and Hyperthermic Perfusion in Treating Patients With Lung Cancer or Lung Metastases That Cannot Be Removed By Surgery
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Heating paclitaxel to several degrees above body temperature and infusing it to the affected area around the tumor may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of paclitaxel given by hyperthermic perfusion in treating patients with lung cancer or lung metastases that cannot be removed by surgery.
Looking for future studies?
Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
NCI - Center for Cancer Research, Bethesda, Maryland, United States
About this study
OBJECTIVES:
- Determine the maximum tolerated dose and phase II dose of paclitaxel administered via hyperthermic retrograde isolated lung perfusion in patients with unresectable pulmonary malignancies.
- Determine the nature of the toxic effects of this regimen in this patient population.
- Evaluate the pharmacokinetic profile of this regimen in these patients.
- Determine the relationship between pharmacodynamic parameters and toxic effects of this regimen in these patients.
OUTLINE: This is a dose-escalation study of paclitaxel.
Patients undergo posterolateral thoracotomy or median sternotomy. Patients receive paclitaxel over 90 minutes administered via hyperthermic retrograde isolated lung perfusion. The entire surgery lasts approximately 4 hours.
Cohorts of 3-6 patients receive escalating doses of paclitaxel until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity.
Patients are followed at 1 and 2 months. Patients with responding disease continue to be followed every 3 months.
PROJECTED ACCRUAL: A maximum of 31 patients will be accrued for this study.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Histologically or cytologically confirmed unresectable primary lung cancer or pulmonary metastases that are unresectable on the basis of technical considerations or are sufficiently numerous that recurrent, potentially inoperable disease is highly probable
- Bilateral metastases allowed
- Unresectable bronchoalveolar carcinomas allowed
- Previously treated primary lung cancer allowed
- Disease outside confines of thorax allowed, provided bulk of disease in the chest is clearly the greatest threat to survival and/or extrathoracic disease is controlled
- No potentially treatable pulmonary metastases from lymphomas or germ cell tumors
- No biopsy proven interstitial fibrosis, radiation induced pneumonitis, or evidence of significant pulmonary hypertension by history, radiologic, echocardiographic, or catheterization studies
- No active intracranial or leptomeningeal metastases
- Prior resection or radiotherapy for intracranial metastases allowed if the following criteria are met:
- No active disease on 2 MRIs done one month apart
- No requirement for anticonvulsant medications or steroids
- Adequate pulmonary reserve to tolerate pneumonectomy:
- Oxygen consumption greater than 50% predicted AND
- FEV1 and DLCO greater than 80% predicted OR
- FEV1 or DLCO less than 80% predicted allowed if postoperative FEV1 and DLCO is at least 40% predicted on the basis of split function V/Q scan
- Prior radiotherapy to chest allowed provided 6 months have elapsed since completion of treatment and no history of, nor current evidence of, interstitial lung disease
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- ECOG 0-1
Life expectancy:
- More than 3 months
Hematopoietic:
- Platelet count greater than 100,000/mm^3
- Hemoglobin greater than 10 g/dL
- WBC greater than 3,500/mm^3
Hepatic:
- PT/PTT normal
- Bilirubin less than 1.5 times upper limit of normal (ULN)
- AST/ALT less than 1.5 times ULN
Renal:
- Creatinine less than 1.6 mg/dL
Cardiovascular:
- Fixed defects on thallium scanning with ejection fraction greater than 40% allowed
- Reversible or ischemic defects allowed only after cardiology clearance
Pulmonary:
- See Disease Characteristics
- Resting oxygen saturation greater than 90%
- pCO_2 less than 45 mmHg by arterial blood gas
Other:
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- No active infections
- HIV negative
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- More than 30 days since prior biologic therapy for this malignancy
Chemotherapy:
- More than 30 days since prior chemotherapy for this malignancy
- Prior paclitaxel allowed
- No prior bleomycin, nitrosoureas, or busulfan
Endocrine therapy:
- See Disease Characteristics
Radiotherapy:
- See Disease Characteristics
Surgery:
- See Disease Characteristics
- Prior thoracic surgery allowed
Treatment and study plan
paclitaxel
DrugHyperthermia Treatment
ProcedureSponsors and collaborators
Lead sponsor
National Cancer Institute (NCI)
Nih
Registry information
Official study title
A Phase I Study of Isolated Lung Perfusion With Paclitaxel and Moderate Hyperthermia in Patients With Unresectable Pulmonary Malignancies
Important dates
- Study start
- 1999
- First posted
- Jan 27, 2003
- Registry last updated
- Apr 29, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Inhaled Doxorubicin in Treating Patients With Primary Lung Cancer or Lung Metastases
NCT00004930
Adenocarcinoma, Adenocarcinoma of Lung
New York, United States
View Trial DetailsTemozolomide and Radiation Therapy in Treating Patients With Brain Metastasis Secondary to Non-Small Cell Lung Cancer
NCT00080938
Adenocarcinoma, Adenocarcinoma of Lung
View Trial DetailsRomidepsin and Erlotinib Hydrochloride in Treating Patients With Stage III or Stage IV Non-Small Cell Lung Cancer
NCT01302808
Adenocarcinoma, Adenocarcinoma of Lung
Dallas, Texas, United States
View Trial DetailsRadiofrequency Ablation in Treating Patients With Refractory or Advanced Lung Cancer
NCT00024076
Adenoma, Bronchial Neoplasms
Los Angeles, California, United States
View Trial Details