ECOG OPERATIONS OFFICE

西非经共体行动办公室的总体目标是提供 领导和支持多学科临床试验 旨在改善癌症治疗。 为了实现这一目标， 目标如下： A. 通过减少滞后时间提高临床试验效率 方案制定、表格制定和方案审查; 开发（计算机）在线随机访问和检查表; 以及取消不必要的注册要求， 要求和后续测量。 B。 通过将我们的技术融入到我们的 现代癌症生物学的临床试验要素，包括 生物反应调节剂，生长因子，免疫化学， 癌基因的分子探针和细胞遗传学。 C. 为我们的MOC和DOC主席提供资源， 制定方案，启动实验室 项目，监测审判的进行，并规划新的 问题研究 D. 提高患者对主要协议的参与率，例如 NCI高优先级倡议、3期试验和生殖泌尿系统 通过提供行政和财政支持， 新的或已建立的参与者的患者。

The overall goal of the ECOG Operations Office is to provide leadership and support for multi disciplinary clinical trials designed to improve cancer therapy. To achieve this the specific aims are as follows: A. Improving clinical trials efficiency by diminishing lag times in protocol development, forms development, and protocol review; developing (computer) on-line randomization access and checklists; and eliminating unnecessary requirements for registration, on study requirements and follow up measurements. B. Initiating new scientific thrusts by incorporating into our clinical trials elements of modern cancer biology, including biologic response modifier agents, growth factors, immunochemistry, molecular probes for oncogenes, and cytogenetics. C. Providing resources to our MOC and DOC chairs to support protocol development, to initiate implementation of laboratory projects, to monitor the conduct of trials, and to plan for new studies. D. Enhancing the accrual of patients into major protocols such as the NCI high priority initiatives, Phase 3 trials and Genitourinary cancers by providing administrative and fiscal support to enlist patients from new or established participants.