Dose-Escalation Study of TH-302 in Combination With Doxorubicin to Treat Patients With Advanced Soft Tissue Sarcoma

ImmunoGenesis

Status and phase

Completed

Phase 2

Phase 1

Conditions

Soft Tissue Sarcoma

Treatments

Drug: TH-302

Study type

Interventional

Funder types

Industry

Identifiers

NCT00742963

TH-CR-403

Details and patient eligibility

About

The purpose of this study is to determine whether TH-302 in combination with Doxorubicin is safe and effective in the treatment of Advanced Soft Tissue Sarcoma.

Full description

A broad range of tumors have been shown to contain significant numbers of hypoxic cells and hypoxia has been shown to be associated with a poor prognosis and an increase in resistance to chemotherapy and radiotherapy (Brizel 1997, Vaupel 2007, Shannon 2003).

It is likely that an agent that could effectively target hypoxic regions in tumors would improve efficacy when combined with standard chemotherapy or radiotherapy. TH-302 is activated at lower oxygen concentrations than other bioreductive prodrugs (Duan 2008) and tirapazamine, a hypoxic cytotoxin that has been extensively studied in both preclinical and clinical studies. This should result in an improved therapeutic ratio (tumor vs normal tissue toxicity) as compared with other bioreductive agents. Because TH-302 is expected to be minimally toxic to aerobic cancer cells, optimal efficacy would be expected when TH-302 is combined with treatments that are most effective under aerobic conditions such as radiotherapy and cytotoxic chemotherapy. Preclinical data have shown at least additive efficacy when TH-302 is combined with chemotherapy. In order to minimize the risk of additive toxicity, TH-302 is not being evaluated in combination with alkylating agents. The study will enroll subjects with advanced soft tissue sarcoma. These tumors have evidence supporting the presence of hypoxia based on pO2 histography, F-MISO and gene expression profiling (Vaupel 2007, Francis 2007, Rajendran 2003).

Enrollment

107 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

All Subjects:

At least 18 years of age
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's IRB/Ethics Committee
Pathologically confirmed diagnosis of soft tissue sarcoma of the following subtypes:
Synovial sarcoma
High grade fibrosarcoma
Unclassified, undifferentiated sarcoma
Liposarcoma
Leiomyosarcoma (excluding GIST)
Angiosarcoma (excluding Kaposi's sarcoma)
Pleomorphic sarcoma/malignant fibrous histiocytoma
Locally advanced unresectable or metastatic disease with no standard curative therapy available and for whom treatment with single agent doxorubicin is considered appropriate; subjects in the dose escalation cohorts must have progressed since their most recent systemic therapy
Recovered from reversible toxicities of prior therapy
Evaluable disease by RECIST criteria (at least one target or non-target lesion for dose escalation cohorts; at least 1 target lesion for dose expansion cohort)
ECOG performance status of 0 or 1
Life expectancy of at least 3 months
Acceptable liver function:
Bilirubin ≤ 1.5 times upper limit of normal (ULN)
AST (SGOT) and ALT (SGPT) ≤ 2.5 times ULN
Acceptable renal function:
Serum creatinine within normal limits
Acceptable hematologic status (without hematologic support):
ANC ≥ 1500 cells/μL
Platelet count ≥ 100,000/μL
Hemoglobin ≥ 9.0 g/dL
Acceptable cardiac function:
Normal 12-lead ECG (clinically insignificant abnormalities permitted)
LVEF normal by MUGA or echocardiogram
Urinalysis: No clinically significant abnormalities
All women of childbearing potential must have a negative serum pregnancy test and all subjects must agree to use effective means of contraception (surgical sterilization or the use or barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel or an IUD) with their partner from entry into the study through 6 months after the last dose

Exclusion Criteria

Prior therapy:

Dose escalation cohort: Prior treatment with more than 2 myelosuppressive cytotoxic chemotherapy regimens
Expanded cohort: Prior systemic therapy for advanced disease (neoadjuvant and adjuvant permitted)
Low grade tumors according to standard grading systems (eg AJCC Grade 1 and 2)
Prior therapy with ifosfamide or cyclophosphamide
Prior therapy with an anthracycline or anthracenedione
Prior mediastinal/cardiac radiotherapy
Current use of drugs with known cardiotoxicity or known interactions with doxorubicin (see product label)
Anticancer treatment with radiation therapy, chemotherapy, targeted therapies (erlotinib, lapatinib, etc.), immunotherapy, hormones or other antitumor therapies within 4 weeks prior to study entry (6 weeks for nitrosoureas or mitomycin C)
Significant cardiac dysfunction:
Any history of congestive heart failure
Any history of transmural myocardial infarction
Uncontrolled arrhythmias within the past 6 months
Angina pectoris requiring antianginal medication within the past 6 months
Clinically significant valvular heart disease
Poorly controlled hypertension within the last 6 months
Seizure disorders requiring anticonvulsant therapy
Known brain metastases (unless previously treated and well controlled for a period of ≥ 3 months) Previously treated malignancies, except for adequately treated non-melanoma skin cancer, in situ cancer, or other cancer from which the subject has been disease-free for at least 5 years
Severe chronic obstructive or other pulmonary disease with hypoxemia (requires supplementary oxygen, symptoms due to hypoxemia or oxygen saturation <90% by pulse oximetry after a 2 minute walk) or in the opinion of the investigator any physiological state likely to cause normal tissue hypoxia
Major surgery, other than diagnostic surgery, within 4 weeks prior to Day 1, without complete recovery
Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
Prior therapy with an hypoxic cytotoxin
Subjects who participated in an investigational drug or device study within 28 days prior to study entry
Known infection with HIV, hepatitis B, or hepatitis C
Subjects who have exhibited allergic reactions to a structural compound, biological agent, or formulation (containing solutol and/or propylene glycol) similar to TH-302
Females who are pregnant or breast-feeding
Concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study
Unwillingness or inability to comply with the study protocol for any reason