Journal
CLINICAL CANCER RESEARCH
Volume 16, Issue 10, Pages 2861-2871Publisher
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-10-0569
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Funding
- NIH [NIH 5 T32 CA009666]
- Melanoma Research Alliance Established Award
- UTMDACC Physician-Scientist Program Award
- Gillson Longenbaugh Foundation
- Carl C. Anderson Sr. & Marie Jo Anderson Charitable Foundation
- Doris Duke Clinical Scientist Development Award
- Bristol-Myers Squibb (BMS)
- Ludwig Trust
- Goodwin-Commonwealth Fund for Cancer Research
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Purpose: Cytotoxic T lymphocyte associated antigen (CTLA-4) blockade is being explored in numerous clinical trials as an immune-based therapy for different malignancies. Our group conducted the first pre-operative clinical trial with the anti-CTLA-4 antibody ipilimumab in 12 patients with localized urothelial carcinoma of the bladder. Experimental Design: Six patients were treated with 3 mg/kg/dose of anti- CTLA-4 and six patients were treated with 10 mg/kg/dose of antibody. Primary end points of the study were safety and immune monitoring. Results: Most drug-related adverse events consisted of grade 1/2 toxicities. All patients had measurable immunologic pharmacodynamic effects, consisting of an increased frequency of CD4(+)ICOS(hi) T cells in tumor tissues and the systemic circulation. To determine if CD4(+)ICOS(hi) T cells could be a correlative marker for clinical outcome after treatment with anti-CTLA-4, a cohort of metastatic melanoma patients was studied retrospectively for frequency of CD4(+)ICOS(hi) T cells and survival. Data from this small cohort of patients indicated that an increased frequency of CD4(+)ICOS(hi) T cells, sustained over a period of 12 weeks of therapy, correlates with increased likelihood of clinical benefit consisting of overall survival. Conclusions: Our trial shows that anti-CTLA-4 therapy has a tolerable safety profile in the presurgical setting and that a preoperative model can be used to obtain biological data on human immune responses, which can efficiently guide the monitoring of patients treated in the metastatic disease setting. Clin Cancer Res; 16(10); 2861-71. (C) 2010 AACR.
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