This trial is active, not recruiting.

Condition melanoma (skin)
Treatment cp-675,206
Phase phase 2
Sponsor Jonsson Comprehensive Cancer Center
Collaborator National Cancer Institute (NCI)
Start date January 2007
End date July 2011
Trial size 34 participants
Trial identifier NCT00471887, CDR0000543416, P30CA016042, PFIZER-UCLA-0606093-01, UCLA-0606093-01


RATIONALE: Monoclonal antibodies, such as ticilimumab (CP-675,206), can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them.

PURPOSE: This phase II trial is studying how well ticilimumab (CP-675,206) works in treating patients with stage IIIC or stage IV melanoma.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Intervention model single group assignment
Masking open label
Primary purpose treatment
See intervention descriptions
Patients will receive intravenous administration of CP-675,206 at a dose of 15mg/kg on Day 1 of an every 90 day cycles. For purposes of treatment visits and scheduling, each cycle is defined as a 90 day period. Patients may receive up to 8 dose (8 cycles) in a 24-month period until progression of disease or intolerable toxicity.

Primary Outcomes

Change in percent tumor infiltration by CD8 positive cytotoxic T lymphocytes
time frame: 4 years

Secondary Outcomes

Tumor evaluation for other immune cell infiltration and melanoma markers
time frame: 4 years
Differences in morphological and gene expression profiling studies in peripheral blood mononuclear cells
time frame: 4 years
Changes in the protein content in peripheral blood with an increase in proinflammatory cytokines and chemokines
time frame: 4 years
Overall response (complete or partial response) as measured by RECIST criteria
time frame: 4 years
Overall safety profile and tolerability as measured by NCI CTCAE v3.0
time frame: 4 years

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - Histologically confirmed melanoma that is surgically incurable and either: - Stage IIIc melanoma including locally relapsed, satellite, in-transit lesions or bulky draining lymph node metastasis. - Stage IV melanoma (M1a, M1b, M1c) with accessible lesions for biopsy. - At least 2 lesions amenable for outpatient biopsies - No restriction based on prior treatments - Disease progression after the last dose of prior therapy - A minimum of one measurable lesion defined as: - Meeting the criteria for measurable disease according to Response Evaluation Criteria in Solid Tumors - Skin lesion(s) selected as non-completely biopsied target lesions that can be accurately measured and recorded by color photography with a ruler to document the size of the target lesion(s). - ECOG performance status 0 or 1 - Adequate bone marrow and hepatic function determined within 30 days prior to enrollment, defined as: - Absolute neutrophil count > 1.0 x 10^9 cells/L - Platelets > 90 x 10^9 /L - Hemoglobin > 9 g/L - Aspartate and alanine aminotransferases < 2.5 x ULN (< 5 x ULN, if documented liver metastases are present) - Total bilirubin < 2 x ULN (except patients with documented Gilbert's syndrome) - Must be willing and able to provide writing informed consent. - Must be willing and able to accept at least two tumor biopsies. - Must be willing and able to accept at least two leukapheresis procedures. Exclusion Criteria: - Received treatment for cancer, including immunotherapy, within one month prior to dosing. - Previous participation in Pfizer study A3671009: A Phase 3, Open Label, Randomized Comparative Study of CP-675,206 and Either Dacarbazine or Temozolomide in Patients with Advanced Melanoma - Eligible for enrollment to Pfizer A3671008: A Phase 2, Open Label, Single Arm Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of CP-675,206 in Patients with Advanced Refractory and/or Relapsed Melanoma - History of significant evidence of risk for chronic inflammatory or autoimmue disease. Patents will be eligible if prior autoimmune disease of the hypophysis was treated locally or have resulted in fibrotic damage requiring thyroid hormone replacement. Vitiligo will not be a basis for exclusion. - History of inflammatory bowel disease, celiac disease, or other chronic gastrointestinal conditions associated with diarrhea or bleeding, or current acute colitis or any origin - Potential requirement for systemic corticosteroids or concurrent immunosuppressive drugs based on prior history or received systemic steroids within the last 4 weeks prior to enrollment - Dementia or significantly altered mental status that would prohibit the understanding or rendering of informed consent and compliance with the requirements of this protocol - Clinically active brain metastases. Radiological documentation of absence of brain metastases at screening is required for all patients - Pregnancy or breast-feeding.

Additional Information

Official title A Phase II, Open-Label, Single Arm Clinical Trial to Study the Mechanism of Action of CP-675,206 in Patients With In-Transit and Metastatic Melanoma Amenable to Repeated Outpatient Tumor Biopsies
Principal investigator Antoni Ribas, MD
Description OBJECTIVES: Primary - Determine the change in melanoma intratumoral infiltrates by CD8 positive cytotoxic T lymphocytes in patients with stage IIIC or IV melanoma treated with ticilimumab (CP-675,206). Secondary - Determine the effects of this drug on intratumoral immune effector cells and tumor cells in these patients. - Determine the effects of this drug on circulating immune effector cells in these patients. - Determine the gene expression profile of immune effector cells and tumor cells in regressing and nonregressing tumors in these patients. - Bank plasma from peripheral blood obtained from patients with regressing and nonregressing tumors for future exploratory analysis of proteomic profile. - Assess additional evidence of antitumor activity of this drug, as measured by best on-study response rate, in these patients. - Characterize the safety profile and tolerability of this drug in these patients. - Obtain pharmacokinetic data to be used in a future meta-analysis of this drug's pharmacokinetics. - Determine whether the CTLA4 genotype influences the safety, immune response, and/or efficacy of this drug in these patients. - Determine the relationships between clinical response (i.e., efficacy or toxicity) and tumor and/or blood ex vivo analysis in patients treated with this drug. OUTLINE: This is an open-label, randomized study. Patients receive ticilimumab (CP-675,206) IV over 2 hours on day 1. Treatment repeats every 90 days for up to 8 courses in the absence of disease progression or unacceptable toxicity. Patients undergo blood collection periodically during study for correlative pharmacokinetic (PK), pharmacogenetic, and pharmacogenomic analyses. Blood specimens are obtained for PK measurement at baseline and periodically during study treatment for analysis by enzyme-linked immunosorbent assay. Blood specimens are also evaluated by pharmacogenetic assessment of polymorphisms in CTLA4. Patients also undergo leukapheresis at baseline and at least once between days 30-60 for biomarker analysis of immune cell activation (i.e., CD45RO, CD45RA, HLA-DR, CCR5, CCR7, CD62L, CD69); Treg phenotype (i.e., CD4/CD25/GITR/intracellular FoxP3); and Treg function. In HLA-A2.1 positive patients, PBMC are analyzed for antigen-specific immune reactivity by MART-1, gp100, and tyrosine MHC tetramer using enzyme-linked immunosorbent spot assay. Plasma obtained during leukapheresis is assessed for levels of circulating cytokines and chemokines. Some plasma is stored for future proteomic profile analysis. Patients also undergo excisional or punch biopsy at baseline and between days 30-60 during course 1. Tumor tissue samples embedded in paraffin are analyzed by hematoxylin-eosin and immunohistochemical staining for several biomarkers, including biomarkers of immune cell response (i.e., CD3, CD4, and CD8) and biomarkers of melanoma (i.e., S-100, MART-1, and/or HMB45). Frozen tumor tissue samples are analyzed by gene chips and gene arrays for gene expression profile and by quantitative real-time polymerase chain reaction for FoxP3. Minced tumor tissue samples are analyzed by flow cytometry in nonadherent cells for HLA-DR (if tumor-infiltrating lymphocytes are available) and by Braf sequencing in adherent cells (if melanoma cells are available). After completion of study therapy, patients are followed every 6 months. PROJECTED ACCRUAL: A total of 21 patients will be accrued for this study.
Trial information was received from ClinicalTrials.gov and was last updated in October 2015.
Information provided to ClinicalTrials.gov by Jonsson Comprehensive Cancer Center.