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Reporting clinical trial information: Colorectal cancer trials at Sydney Cancer Centre

机译:报告临床试验信息:悉尼癌症中心的大肠癌试验

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Background: Clinical trial units are integral to the functioning of a medical oncology department with patient access to clinical trials an important component in patient care. There has been a paucity of potential key performance indicators in medical oncology and clinical trial information may be utilised for this purpose. The aim of this study was to record retrospectively and collate prospectively collected information regarding basic demographics, response rate, progression and survival plus grade 3 or 4 toxicity in patients enrolled in clinical trials for metastatic colorectal cancer at the Sydney Cancer Centre between 1999 and 2007. Methods: Baseline patient demographics, clinical response, progression dates, grade 3 or 4 toxicities plus treatment-related fatalities were collected from individual clinical trials. Outcome measures were clinical response, progression-free survival and overall survival. Results: There was a total of 14 trials undertaken during the defined period for patients with metastatic colorectal cancer. There was available information for 243 patient trials with sufficient information regarding response rates, toxicity, progression and survival. Tumour response rates ranged from 27% to 66% for first line chemotherapy trials and 0% to 20% for non-first line chemotherapy trials. The overall progression-free survival was 6.4months and overall survival 14.0months for all trials. There was one treatment-related fatality on clinical trial during this period. Conclusions: Results of our clinical database have been used here to illustrate the concept and value of reporting clinical trial information in medical oncology. Public reporting of such information may allow for comparisons between units and for quality improvement.
机译:背景:临床试验单位是医学肿瘤学部门不可或缺的组成部分,患者获得临床试验的机会是患者护理中的重要组成部分。医学肿瘤学中潜在的关键性能指标很少,因此可将临床试验信息用于此目的。这项研究的目的是回顾性记录和整理前瞻性收集的有关1999年至2007年间在悉尼癌症中心接受转移性结直肠癌临床试验的患者的基本人口统计学,缓解率,进展和生存率以及3级或4级毒性的信息。方法:从单个临床试验中收集基线患者的人口统计学,临床反应,进展日期,3或4级毒性以及与治疗相关的死亡。结果指标是临床反应,无进展生存期和总生存期。结果:在确定的时期内,共进行了14项针对转移性结直肠癌患者的试验。有243例患者试验的可用信息,其中包含有关缓解率,毒性,进展和生存的充分信息。一线化疗试验的肿瘤反应率范围为27%至66%,非一线化疗试验的肿瘤反应率范围为0%至20%。所有试验的总无进展生存期为6.4个月,总生存期为14.0个月。在此期间,临床试验中有1位与治疗相关的死亡。结论:我们的临床数据库结果已用于说明医学肿瘤学中报告临床试验信息的概念和价值。此类信息的公开报告可能允许单位之间进行比较并提高质量。

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