A Phase I Study of OncoLAR® (Registered Trademark) (NSC 685403) With/Without Tamoxifen in Patients With Osteosarcoma
OncoLAR® (Registered Trademark)
+ tamoxifen
Neoplasms+10
+ Neoplasms by Histologic Type
+ Neoplasms, Connective Tissue
Treatment Study
Summary
Study start date: May 1, 1995
Actual date on which the first participant was enrolled.Osteosarcoma is the most common primary bone malignancy in childhood and adolescence. Its peak age of onset has suggested a possible contribution to the pathogenesis of the tumor by the endogenous hormonal milieu, which accompanies the adolescent growth spurt. In support of this, recent in vitro and in vivo laboratory investigators suggest that Insulin-like growth factor I (IGF I) may play an important role in the pathobiology of osteosarcoma. Somatostatin (and its longer-acting analogues) directly inhibits the pituitary release of growth hormone, thereby indirectly reducing the level of circulating IGF I. Other data have also demonstrated that the anti-estrogen, tamoxifen, significantly reduced circulating IGF I levels. We propose to administer the long acting somatostatin analog, OncoLAR® (Registered Trademark), alone and in combination with tamoxifen in patients with osteosarcoma. The degree of suppression of both circulating IGF I and growth hormone levels will be determined at two dose levels of OncoLAR® (Registered Trademark) alone and in combination with tamoxifen to determine whether the addition of tamoxifen to OncoLAR® (Registered Trademark) leads to significant additional reduction in circulating IGF I and growth hormone levels.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.24 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Must have been diagnosed with osteosarcoma by the age of 25 years. Patient must have a biopsy proven osteosarcoma and either: a) active tumor with no available standard therapy options; b) metastatic osteosarcoma at diagnosis, has completed therapy and has no evidence of active disease; or, c) is status-post any surgery for recurrent osteosarcoma, either local or metastatic recurrence, and is free of disease by CT scan. Measurable disease not required. Patients with serum creatinine <e; 2.0 mg/dL or creatinine clearance >e; 40 ml/min per 1.73m(2) (if serum creatinine is >e; 2.0 mg/dL). Patients with normal thyroid function. Patients with total bilirubin, SGOT and SGPT < twice the upper limit of normal. Patients with normal direct bilirubin only if total direct bilirubin is abnormal. Patients with bone marrow criteria: ANC>1500/mm(3) and platelet count >100,000/mm(3). Patients without a history of insulin-dependent diabetes mellitus or current insulin requirement. Fasting morning blood glucose <150 mg/dL. Patients with ECOG performance status of 0, 1 or 2 and a life expectancy of at least 8 weeks. Patients not on chemotherapy or radiation therapy within the past 2 weeks and recovered from the acute side effects of prior anti-neoplastic therapy. Patients with documented negative HIV serology within the past 6 months. Post-menarcheal patients must have documented negative urine and serum pregnancy test (B-HCG); when indicated, patient must be willing to take oral contraceptives or other appropriate contraceptives to avoid pregnancy during the period of treatment. Patient, parent or guardian must give informed consent. No pregnant or lactating women. No women of child-bearing potential who are unable or unwilling to use appropriate contraceptives during the period of treatment. No patients with uncorrected hypothyroidism. No patients with insulin-dependent diabetes mellitus or fasting blood glucose >e; 150 mg/dL. No patients with HIV infection. No patients with a history of thromboembolic events who require prophylaxis for thromboembolic events with anticoagulants once entry into Cohort III has begun. Patients with a history of symptomatic gallbladder disease must have had a cholecystectomy.
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
National Cancer Institute (NCI)
Bethesda, United StatesOpen National Cancer Institute (NCI) in Google Maps