Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

New York, New York 10065


This phase I trial is studying the side effects and best dose of alvocidib when given with doxorubicin hydrochloride in treating patients with metastatic or recurrent sarcoma that cannot be removed by surgery. Drugs used in chemotherapy, such as doxorubicin hydrochloride and alvocidib, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Alvocidib may also help doxorubicin hydrochloride work better by making tumor cells more sensitive to the drug. Giving more than one drug may kill more tumor cells

Study summary:

PRIMARY OBJECTIVE: I. Determine the maximum tolerated dose of flavopiridol (alvocidib) when administered with a fixed dose of doxorubicin (doxorubicin hydrochloride) in patients with unresectable metastatic or locally recurrent sarcoma. SECONDARY OBJECTIVES: I. Determine the clinical pharmacokinetics of this regimen in these patients. II. Determine, preliminarily, the therapeutic activity of this regimen in these patients. III. Correlate pRb, p53, and p21 protein levels with treatment response and apoptosis in patients treated with this regimen. IV. Correlate NMR biochemical patterns with response in patients treated with this regimen. OUTLINE: This is an open-label, dose-escalation study of alvocidib. Patients receive doxorubicin hydrochloride intravenously (IV) over 5-10 minutes and alvocidib IV over 1 hour on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients reaching a cumulative doxorubicin dose of 600 mg/m^2 or experiencing cardiotoxicity may receive alvocidib alone at the discretion of the investigator. Cohorts of 3-6 patients receive escalating doses of alvocidib until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Ten additional patients receive treatment at the MTD. Patients are followed every 3 months for 1 year.


Inclusion Criteria: - Histologically or cytologically confirmed soft-tissue sarcoma* - Unresectable disease - Locally recurrent or metastatic disease - Disease amenable to biopsy (patients treated at the maximum tolerated dose only) - No known prior or concurrent brain metastases - Performance status - Karnofsky 60-100% - Performance status - ECOG 0-2 - Absolute neutrophil count ≥ 1,500/mm^3 - Platelet count ≥ 100,000/mm^3 - Bilirubin ≤ 1.5 mg/dL - AST and ALT ≤ 2.5 times upper limit of normal - Creatinine ≤ 1.5 mg/dL - Creatinine clearance ≥ 60 mL/min - Ejection fraction ≥ 50% by MUGA or echocardiogram - No uncontrolled hypertension - No myocardial infarction - No New York Heart Association class II-IV congestive heart failure - No unstable angina - No serious cardiac arrhythmia requiring medication - No peripheral vascular disease ≥ grade 2 within the past year - No other clinically significant cardiac disease - No prior deep vein thrombosis - No other prior vascular thrombus - No prior pulmonary embolism - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception - No symptomatic peripheral neuropathy ≥ grade 2 - No other malignancy within the past 5 years except adequately treated basal cell skin cancer or carcinoma in situ of the cervix - Carcinoma in situ not considered a second malignancy - No history of allergic reaction attributed to compounds of similar chemical or biologic composition to study drugs - No psychiatric illness or social situation that would preclude study compliance - No ongoing or active infection - No other uncontrolled illness - See Chemotherapy - At least 3 weeks since prior immunotherapy and recovered - At least 3 weeks since prior chemotherapy (6 weeks for carmustine or mitomycin) and recovered - No more than 2 prior cytotoxic chemotherapy regimens - Peroxisome proliferator-activated receptor (PPAR)-gamma agonists, thalidomide, or targeted therapy (i.e., tyrosine kinase inhibitors including imatinib mesylate, sorafenib, or sunitinib malate) do not count as a prior chemotherapy regimen - No prior anthracyclines - At least 3 weeks since prior radiotherapy and recovered - No prior extensive radiotherapy to bone marrow-producing sites (e.g., radiotherapy to both the pelvis and spine) - At least a 1 week washout period since prior tyrosine kinase inhibitors or other targeted therapy - Concurrent low-dose warfarin (1 mg per day) to prevent thrombus of a central line allowed - No concurrent combination antiretroviral therapy for HIV-positive patients - No other concurrent investigational agents - No other concurrent anticancer therapy



Primary Contact:

Principal Investigator
David D'Adamo
Memorial Sloan-Kettering Cancer Center

Backup Contact:


Location Contact:

New York, New York 10065
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.

Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.