Amrubicin Chemotherapy as First Line in Metastatic or Unresectable Soft Tissue Sarcoma

NCT ID: NCT01259375

Last Updated: 2017-04-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-09-30
• Study Completion Date: 2016-02-29

Brief Summary

Primary Objectives

1. To evaluate the Response Rate (RR) for amrubicin in patients with metastatic or advanced sarcoma as first line therapy.

2. To evaluate Progression Free Survival (PFS).

Secondary Objectives

1. To assess the safety and tolerability of amrubicin in this patient population.

2. To evaluate whether certain histologic subtypes of sarcoma demonstrate a differential response to amrubicin.

3. To investigate quality of response with radiographic evaluation using both Response Evaluation Criteria In Solid Tumors (RECIST) and Choi criteria.

4. To evaluate overall survival (OS).

Conditions

Soft Tissue Sarcoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

All patients

All participants who received Amrubicin.

Group Type: EXPERIMENTAL

Amrubicin

Intervention Type: DRUG

Synthetic 9-aminoanthracycline Patients will receive 40mg/m2/day intravenously

Interventions

Amrubicin

Synthetic 9-aminoanthracycline Patients will receive 40mg/m2/day intravenously

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Adult patients (age 18 years or older)
• Pathological diagnosis of soft tissue sarcoma. Pathology materials must be submitted and reviewed.
• Patients must have unresectable locally advanced or metastatic progressive disease prior to enrollment. Disease extent must be determined by scans (CT or PET CT) within 6 weeks of enrollment.
• No prior chemotherapy for soft tissue sarcoma.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
• Adequate organ function including the following:
• Adequate bone marrow reserve: absolute neutrophil count (segmented and bands) (ANC) 1.5 x 109/L, platelet count 100 x 109/L, and hemoglobin 90 g/L,
• Hepatic: bilirubin 1.5 x the upper limit of normal (ULN), ALT and AST 3.0 x ULN,
• Renal: serum creatinine 1.5 x ULN or calculated creatinine clearance greater than 60 mL/min,
• Cardiac: Left ventricular ejection fraction (LVEF) 50% by echocardiogram (ECHO) or multiple gated acquisition scan (MUGA);
• All labs must be done within 2 weeks prior to enrollment.
• Negative serum pregnancy test at the time of enrollment for females of childbearing potential;
• For males and females of child-producing potential, use of effective contraceptive methods during the study;
• Ability to understand the requirements of the study and provide written informed consent.

Exclusion Criteria

• Pregnant or nursing females
• Chest radiotherapy with curative intent to the primary disease complex less than or equal to 28 days prior to first dose; cranial radiotherapy less than or equal to 21 days prior to first dose; radiotherapy to all other areas less than or equal to 7 days prior to first dose
• Concurrent severe or uncontrolled medical disease (eg, active systemic infection, diabetes, hypertension, coronary artery disease, congestive heart failure, active viral hepatitis or chronic liver disease) that, in the opinion of the investigator, would compromise the safety of the patient or compromise the ability of the patient to complete the study
• Symptomatic central nervous system metastases. Patients with asymptomatic brain metastases are allowed. The patient must be stable for 2 weeks after radiotherapy; if the patient is on corticosteroids, the dose of corticosteroids must have been stable for 2 weeks prior to first dose of study treatment, or be in the process of being tapered
• Suspected, diffuse idiopathic interstitial lung disease or pulmonary fibrosis.
• Patients with known history of seropositive human immunodeficiency virus (HIV) or patients who are receiving immunosuppressive medications that would, in the opinion of the investigator, increase the risk of serious neutropenic complications. HIV testing is not required for inclusion in the trial.
• Known hypersensitivity to any of the components of the i.v. formulation of amrubicin.
• Psychiatric disorder or any other personal circumstances that prevent compliance with the study protocol.
• Inability or unwillingness to comply with the study protocol.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Utah

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Santa Monica

Santa Monica, California, United States

Huntsman Cancer Institute

Salt Lake City, Utah, United States

Countries

United States

Other Identifiers

HCI45197

Identifier Type: -

Identifier Source: org_study_id