Ignite Creation Date:
2025-12-25 @ 12:34 AM
Ignite Modification Date:
2025-12-25 @ 10:42 PM
Study NCT ID:
NCT00061867
Status:
COMPLETED
Last Update Posted:
2013-05-30
First Post:
2003-06-05
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Liposomal Doxorubicin and Thermal Therapy in Treating Patients With Prostate Cancer
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D011471', 'term': 'Prostatic Neoplasms'}], 'ancestors': [{'id': 'D005834', 'term': 'Genital Neoplasms, Male'}, {'id': 'D014565', 'term': 'Urogenital Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D005832', 'term': 'Genital Diseases, Male'}, {'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D011469', 'term': 'Prostatic Diseases'}, {'id': 'D052801', 'term': 'Male Urogenital Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D003972', 'term': 'Diathermy'}], 'ancestors': [{'id': 'D006979', 'term': 'Hyperthermia, Induced'}, {'id': 'D013812', 'term': 'Therapeutics'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT'}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2003-03'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2005-07', 'completionDateStruct': {'date': '2005-08', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2013-05-29', 'studyFirstSubmitDate': '2003-06-05', 'studyFirstSubmitQcDate': '2003-06-05', 'lastUpdatePostDateStruct': {'date': '2013-05-30', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2003-06-06', 'type': 'ESTIMATED'}}, 'conditionsModule': {'keywords': ['adenocarcinoma of the prostate', 'stage III prostate cancer', 'stage IV prostate cancer'], 'conditions': ['Prostate Cancer']}, 'descriptionModule': {'briefSummary': 'RATIONALE: Drugs used in chemotherapy, such as liposomal doxorubicin, use different ways to stop tumor cells from dividing so they stop growing or die. Microwave thermotherapy kills tumor cells by heating them to several degrees above body temperature. Combining liposomal doxorubicin with microwave thermotherapy may kill more tumor cells.\n\nPURPOSE: This phase I trial is studying the side effects and best dose of liposomal doxorubicin when given together with microwave thermotherapy in treating patients with prostate cancer.', 'detailedDescription': 'OBJECTIVES:\n\n* Determine the maximum tolerated dose of doxorubicin HCl liposome released through thermal microwave therapy in patients with adenocarcinoma of the prostate.\n* Determine the pharmacokinetics and biodistribution profile of this drug in these patients.\n* Determine the safety profile and dose-limiting toxicity of this drug in these patients.\n* Determine the clinical response in patients treated with this regimen.\n\nOUTLINE: This is an open-label, dose-escalation, multicenter study.\n\nPatients receive doxorubicin HCl liposome IV over 30 minutes. Patients then undergo a 60-minute course of prostate thermotherapy. Treatment may repeat every 28-42 days for up to 6 courses, at the discretion of the physician.\n\nCohorts of 3-6 patients receive escalating doses of doxorubicin HCl liposome until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which at least 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.\n\nPatients are followed at 8, 15, 30, and 90 days.\n\nPROJECTED ACCRUAL: Approximately 50 patients will be accrued for this study.'}, 'eligibilityModule': {'sex': 'MALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '40 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'DISEASE CHARACTERISTICS:\n\n* Histologically confirmed adenocarcinoma of the prostate\n* Rising prostate-specific antigen AND radiographic evidence of extraprostatic prostate cancer by bone scan, CT scan, prostascint scan, or MRI\n\nPATIENT CHARACTERISTICS:\n\nAge\n\n* 40 and over\n\nPerformance status\n\n* Karnofsky 80-100%\n\nLife expectancy\n\n* Not specified\n\nHematopoietic\n\n* WBC greater than 4,000/mm\\^3\n* Platelet count greater than 100,000/mm\\^3\n* Hemoglobin greater than 10.0 g/dL\n\nHepatic\n\n* Bilirubin normal\n* AST normal\n* Alkaline phosphatase normal\n* No acute or chronic liver disease\n\nRenal\n\n* Creatinine less than 1.5 times upper limit of normal\n\nCardiovascular\n\n* Ejection fraction at least 50% by MUGA\n* EKG normal\n* No myocardial infarction or cerebral vascular accident within the past 6 months\n* No life threatening cardiac arrhythmias\n* No congestive heart failure\n* No cardiac pacemaker\n* No peripheral arterial disease with intermittent claudication or Leriches syndrome (i.e., claudication of the buttocks or perineum)\n\nOther\n\n* Fertile patients must use effective barrier contraception during and for 3 months after study participation\n* No sperm donation during and for 3 months after study participation\n* Not febrile\n* No interest in future fertility or fathering children\n* No significantly decreased pain response\n* No severe urethral stricture\n* No protruding median lobe resulting in a "ball-valve" type of obstruction at the bladder neck\n* No major psychiatric illness that would prevent informed consent\n* No major psychiatric illness that required inpatient treatment within the past 3 months\n* No psychological, family, sociological, or geographic condition that would preclude study compliance\n* No allergy to eggs or egg products\n* No urinary or prostatic infection\n* No full urinary retention\n* No penile or urinary sphincter implant\n* No metallic implants in the pelvic or femoral area\n* No other serious medical illness that would preclude study participation\n\nPRIOR CONCURRENT THERAPY:\n\nBiologic therapy\n\n* No concurrent live vaccines\n\nChemotherapy\n\n* No prior anthracycline\n* No concurrent streptozocin\n\nEndocrine therapy\n\n* No concurrent hormonal therapy (except luteinizing hormone-releasing hormone analog)\n* No concurrent glucocorticoids administered at more than physiologic replacement doses (other than as an antiemetic)\n\nRadiotherapy\n\n* Not specified\n\nSurgery\n\n* More than 3 months since prior major surgery\n\nOther\n\n* No prior therapy that resulted in permanent reduction of pain response (e.g., prior surgery, regional or local anesthetic)\n* No concurrent PC-SPES\n* No concurrent cyclosporine, phenobarbital, or phenytoin'}, 'identificationModule': {'nctId': 'NCT00061867', 'briefTitle': 'Liposomal Doxorubicin and Thermal Therapy in Treating Patients With Prostate Cancer', 'organization': {'class': 'NIH', 'fullName': 'National Cancer Institute (NCI)'}, 'officialTitle': 'A Dose Escalation, Pharmacokinetics, and Safety Study of Doxorubicin Encapsulated in Temperature Sensitive Liposomes Released Through Microwave Therapy in the Treatment of Prostate Cancer', 'orgStudyIdInfo': {'id': 'CELSION-10302101'}, 'secondaryIdInfos': [{'id': 'CDR0000301761', 'type': 'REGISTRY', 'domain': 'PDQ (Physician Data Query)'}, {'id': 'RPCI-DS-0228'}]}, 'armsInterventionsModule': {'interventions': [{'name': 'pegylated liposomal doxorubicin hydrochloride', 'type': 'DRUG'}, {'name': 'hyperthermia treatment', 'type': 'PROCEDURE'}]}, 'contactsLocationsModule': {'locations': [{'zip': '71106', 'city': 'Shreveport', 'state': 'Louisiana', 'country': 'United States', 'facility': 'Regional Urology, L.L.C.', 'geoPoint': {'lat': 32.52515, 'lon': -93.75018}}, {'zip': '29572', 'city': 'Myrtle Beach', 'state': 'South Carolina', 'country': 'United States', 'facility': 'Grand Strand Urology LLP', 'geoPoint': {'lat': 33.68906, 'lon': -78.88669}}], 'overallOfficials': [{'name': 'Catherine Van Doren, RN', 'role': 'STUDY_CHAIR', 'affiliation': 'Imunon'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Imunon', 'class': 'INDUSTRY'}}}}