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Phase 2 Completed N=83 Treatment

A Phase II, Multi-Center, Open-Label, Uncontrolled Study to Evaluate the Efficacy and Safety of Sorafenib Given Daily in Combination With Repeated 21-Day Cycles of Dacarbazine (DTIC) Chemotherapy in Subjects With Advanced Metastatic Melanoma

Source: ClinicalTrials.gov NCT00492297 ↗
Enrolled (actual)
83
Serious AEs
48.2%
Results posted
Jan 2011
Primary outcomePrimary: Overall Best Response — 10; 1; 9; 31 participants

Summary

The purpose of this study is to see whether a new type of anti-cancer drug, known as BAY 43-9006, can be given safely and with good effect in combination with dacarbazine (DTIC). DTIC is the current standard chemotherapy drug given for melanoma that has spread through the body. Although this drug can be effective on its own and is generally well tolerated, not all patients will benefit, so there is a need to test new drugs and drug combinations for treating melanoma.

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Best Response
10; 1; 9; 31; 34
SECONDARY
Progression-free Survival
102
SECONDARY
Percentage of Subjects With Progression-free Survival at Specific Time-points
56.63; 33.73; 10.84
SECONDARY
Overall Survival
259
SECONDARY
Duration of Response
327
SECONDARY
Duration of Complete Response
420
SECONDARY
Duration of Partial Response
255
SECONDARY
Disease Control (DC)
41; 38; 38
SECONDARY
Duration of Stable Disease
93
SECONDARY
Time to Response
48
SECONDARY
Time to Progression
102

Eligibility Criteria

Inclusion Criteria

  • Subjects with advanced, metastatic, histologically confirmed melanoma, for whom treatment with dacarbazine is considered medically acceptable
  • Age >= 18 years
  • Subject has measurable and evaluable disease defined as at least one metastatic lesion that can be accurately and serially measured by Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) scan as per the Response Evaluation Criteria in Solid Tumors (RECIST) criteria. Cutaneous lesions measuring at least 20mm in longest diameter can be considered measurable (and therefore target lesions) via color photography including a ruler
  • Subject has biopsiable disease at baseline and is willing to provide biopsy samples, or does not have biopsiable disease at baseline
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1

Exclusion Criteria

  • Primary ocular or mucosal melanoma (cutaneous vulval melanoma is permitted)
  • Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors [Ta, Tis & T1] or any cancer curatively treated > 3 years prior to study entry
  • (Active coronary artery disease or ischemia (myocardial infarction more than 6 months prior to study entry is allowed)
  • Uncontrolled hypertension (> grade 2 National Cancer Institute - Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 3.0)
  • Active, clinically serious infections (> grade 2 NCI-CTCAE version 3.0)
  • Subjects with seizure disorder requiring medication are excluded
  • History of or suspected Human Immunodeficiency Virus (HIV) infection, or chronic hepatitis B or C
  • Symptomatic metastatic brain or meningeal tumors unless the subject is > 6 months from definitive therapy, has a negative imaging study within 4 weeks prior to study entry and is clinically stable with respect to the tumor at the time of study entry. Also the subject must not be undergoing acute steroid therapy or taper (chronic steroid therapy is acceptable provided that the dose is stable for one month prior to and following screening radiographic studies)
  • Pregnant or breast-feeding subjects
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00492297). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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