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Efficacy and Safety Study of CC-4047 (Pomalidomide) to Treat Advanced Soft Tissue Sarcoma

Phase 2
Terminated
Conditions
Soft Tissue Sarcoma
Interventions
Registration Number
NCT00717522
Lead Sponsor
Celgene
Brief Summary

The purpose of the study is to determine the safety and efficacy of single agent CC-4047 (pomalidomide) in patients with advanced soft tissue sarcomas who have relapsed or are refractory to prior anticancer therapy.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
7
Inclusion Criteria
  • Must be > 18 years of age
  • Must have histologically confirmed soft tissue sarcoma
  • Must have locally recurrent unresectable, or metastatic soft tissue sarcoma, and have failed or relapsed after a minimum of one and a maximum of 3 prior systemic anticancer therapy regimens
  • Must have measurable or evaluable disease determined as per Response Evaluation Criteria in Solid Tumors (RECIST) criteria
  • Must have documented disease progression (PD) determined as per RECIST criteria within 3 months prior to study enrollment
  • Must have Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1
Exclusion Criteria
  • Pregnant or lactating females
  • Prior therapy with thalidomide or lenalidomide
  • Prior use of experimental/investigational drug therapy < 3 months prior to treatment initiation
  • Prior chemotherapy, biologic or immunotherapy < 3 weeks prior to treatment initiation
  • Prior radiotherapy < 3 weeks prior to treatment initiation
  • Prior major surgery < 3 weeks prior to treatment initiation
  • Absolute neutrophil count (ANC) < 1.5 x 109 cells/L
  • Platelet count < 100 x 109cells/L
  • Aspartate aminotransferase/serum glutamic oxaloacetic transaminase (AST/SGOT) and alanine aminotransferase/serum glutamic pyruvate transaminase (ALT/SGPT) > 3.0 x upper limit of normal (ULN) or > 5.0 x ULN in the presence of demonstrable liver metastases
  • Known active central nervous system (CNS) metastases

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
PomalidomidePomalidomide7 mg pomalidomide taken orally once daily (QD) on days 1 through 21 of each 28-day cycle
Primary Outcome Measures
NameTimeMethod
Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Deaths, or Discontinuations Due to AEsAEs/SAEs were recorded from informed consent to 30 days post treatment discontinuation visit. Median treatment duration was 49 days (range: 3 to 102 days).

An adverse event (AE) is defined as any noxious, unintended, or untoward medical occurrence occurring at any dose that may appear or worsen in a study subject during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the study subject's health, including laboratory test values, regardless of etiology. A serious adverse event (SAE) is defined as any AE which: results in death; is life-threatening; requires inpatient hospitalization or prolongation of existing hospitalization; results in persistent or significant disability/incapacity; is a congenital anomaly/birth defect; constitutes an important medical event. National Cancer Institute (NCI) Common Toxicity Criteria for Adverse Events (CTCAE), Version 3.0, grades: 1 = mild, 2 = moderate, 3 = severe, 4 = life threatening, 5 = death. For more details, please see the Adverse Events section of this record.

Secondary Outcome Measures
NameTimeMethod
Tumor Response as Assessed by the Response Evaluation Criteria in Solid Tumors (RECIST) Committee GuidelinesAssessed every 8 weeks for the first 8 months and then every 12 weeks thereafter, and at treatment discontinuation. Median treatment duration was 49 days (range: 3 to 102 days).

Changes in only the longest diameter (LD) of tumor lesions are used in RECIST criteria. Evaluation of target lesions: Complete Response (CR)=Disappearance of all target lesions; Partial Response (PR)=≥30% decrease in sum of the longest diameter (LD) of target lesions taking as reference the baseline sum LD; Progressed Disease (PD)=≥20% increase in sum of LD of target lesions taking as reference the smallest sum LD recorded since treatment started or the appearance of ≥1 new lesions; Stable Disease (SD)=Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as reference the smallest sum LD since treatment started. For non-target lesions: CR= Disappearance of all non-target lesions and normalization of tumor marker level; Incomplete Response/SD=Persistence of ≥1 non-target lesions and/or maintenance of tumor marker level above normal limits; PD=Appearance of ≥1 new lesions; unequivocal progression of existing non-target lesions.

Trial Locations

Locations (3)

Sarcoma Oncology Center

🇺🇸

Santa Monica, California, United States

Kootenai Cancer Center

🇺🇸

Coeur d'Alene, Idaho, United States

Nebraska Methodist Hospital

🇺🇸

Omaha, Nebraska, United States

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