Safety and Efficacy Study of Torisel and Liposomal Doxorubicin for Patients With Recurrent Sarcoma

Johns Hopkins Medicine

Status and phase: Completed; Phase 2; Phase 1

Conditions: Sarcoma

Treatments: Drug: temsirolimus plus liposomal doxorubicin

Study type: Interventional

Funder types: Other; NETWORK; Industry

Identifiers

NCT00949325

NA_00028490 (Other Identifier)

J0963

Details and patient eligibility

About

The purpose of this study is to identify a safe dosing regimen for the combination of Torisel and liposomal doxorubicin in patients with recurrent sarcoma. A secondary purpose of the study is to determine how effective this combination is for the treatment of recurrent sarcoma.

Full description

The effectiveness of treatments for recurrent sarcomas is quite limited. One hypothesis to explain the refractory nature of recurrent sarcomas is the existence of chemotherapy-resistant sarcoma stem cells.

Enrollment: 24 patients

Sex: All

Ages: 1+ year old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed sarcoma that is recurrent or refractory to conventional treatment
• Measurable disease by RECIST criteria
• ECOG (Eastern Cooperative Oncology Group) performance status < 2 (or Lansky/Karnofsky > 60% for children)
• Life expectancy greater than 3 months
• Adequate organ function
• absolute neutrophil count at least 1,500
• platelets at least 100,000
• bilirubin less than 1.5 x upper limit of normal
• AST (aspartate aminotransferase) and ALT(alanine aminotransferase) less than 2.5 x upper limit of normal
• creatinine less than 1.5 x upper limit of normal OR creatinine clearance at least 60 ml/min/1.73 m2
• fasting serum cholesterol less than 350
• fasting serum triglycerides less than 400
• PT (prothrombin) or INR (international normalized ratio) less than 1.3 x upper limit of normal
• normal urinalysis
• Ability to understand and sign the informed consent document

Exclusion criteria

• Prior chemotherapy or radiotherapy within 3 weeks of entering the study (6 weeks for nitrosoureas or mitomycin C)
• Prior treatment with a tyrosine kinase inhibitor within 10 days of entering the study
• History of pulmonary hypertension or pneumonitis
• Patients may not be receiving other investigational agents
• Prior therapy with rapamycin, rapamycin analogues, or tacrolimus
• Uncontrolled brain metastases
• History of grade 3 or 4 hypersensitivity to macrolide antibiotics
• Concurrent treatment with immunosuppressive agents other than a stable (for more than 2 weeks) dose of corticosteroids
• Uncontrolled intercurrent illness
• Pregnancy or breast feeding
• HIV-positive patients on combination antiretroviral therapy
• Grade 3 or 4 proteinuria

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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24 participants in 1 patient group

temsirolimus plus liposomal doxorubicin

Experimental group

Description:

Single arm study: Dose escalation of temsirolimus plus constant dose of liposomal doxorubicin.

Treatment:

Drug: temsirolimus plus liposomal doxorubicin