Department of Surgery and Comprehensive Cancer Center, University of Michigan, Ann Arbor, MI, USA.
Ann Surg Oncol. 2011 Dec;18(13):3544-50. doi: 10.1245/s10434-011-1818-9. Epub 2011 Jun 17.
The clinical trials mechanism of standardized treatment and follow-up for cancer patients with similar stages and patterns of disease is the most powerful approach available for evaluating the efficacy of novel therapies, and clinical trial participation should protect against delivery of care variations associated with racial/ethnic identity and/or socioeconomic status. Unfortunately, disparities in clinical trial accrual persist, with African Americans (AA) and Hispanic/Latino Americans (HA) underrepresented in most studies.
We evaluated the accrual patterns for 10 clinical trials conducted by the American College of Surgeons Oncology Group (ACOSOG) 1999-2009, and analyzed results by race/ethnicity as well as by study design.
Eight of 10 protocols were successful in recruiting AA and/or HA participants; three of four randomized trials were successful. Features that were present among all of the successfully recruiting protocols were: (1) studies designed to recruit patients with regional or advanced-stage disease (2 of 2 protocols); and (2) studies that involved some investigational systemic therapy (3 of 3 protocols).
AA and HA cancer patients can be successfully accrued onto randomized clinical trials, but study design affects recruitment patterns. Increased socioeconomic disadvantages observed within minority-ethnicity communities results in barriers to screening and more advanced cancer stage distribution. Improving cancer early detection is critical in the effort to eliminate outcome disparities but existing differences in disease burden results in diminished eligibility for early-stage cancer clinical trials among minority-ethnicity patients.
为评估新型疗法的疗效,针对疾病分期和类型相似的癌症患者采用标准化治疗和随访的临床试验机制是最有效的方法,参加临床试验应能避免因种族/民族身份和/或社会经济地位不同而导致的治疗差异。遗憾的是,临床试验入组的差异仍然存在,大多数研究中非洲裔美国人(AA)和西班牙裔/拉丁裔美国人(HA)的代表性不足。
我们评估了美国外科医师学会肿瘤学组(ACOSOG)1999 年至 2009 年进行的 10 项临床试验的入组模式,并按种族/民族以及研究设计对结果进行了分析。
10 项方案中有 8 项成功招募了 AA 和/或 HA 参与者;4 项随机试验中有 3 项成功。所有成功招募方案中都具有以下特征:(1)旨在招募局部晚期或晚期疾病患者的研究(2 项方案中的 2 项);(2)涉及某些试验性系统治疗的研究(3 项方案中的 3 项)。
可以成功招募 AA 和 HA 癌症患者参加随机临床试验,但研究设计会影响招募模式。少数族裔社区中观察到的社会经济劣势增加了筛查障碍和更晚期癌症的分布。改善癌症早期检测对于消除结局差异至关重要,但现有疾病负担的差异导致少数族裔患者参与早期癌症临床试验的资格降低。