Preoperative CTLA-4 blockade: tolerability and immune monitoring in the setting of a presurgical clinical trial. Academic Article uri icon

Overview

abstract

  • 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 preoperative 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+ICOShi T cells in tumor tissues and the systemic circulation. To determine if CD4+ICOShi 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+ICOShi T cells and survival. Data from this small cohort of patients indicated that an increased frequency of CD4+ICOShi 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.

publication date

  • May 11, 2010

Research

keywords

  • Antibodies, Monoclonal
  • Antigens, CD
  • Carcinoma, Transitional Cell
  • Neoadjuvant Therapy
  • Urinary Bladder Neoplasms

Identity

PubMed Central ID

  • PMC2919850

Scopus Document Identifier

  • 77952337834

Digital Object Identifier (DOI)

  • 10.1158/1078-0432.CCR-10-0569

PubMed ID

  • 20460488

Additional Document Info

volume

  • 16

issue

  • 10