Bastyr Integrative Oncology Research Center, Bastyr University, 14500 Juanita Dr NE, Kenmore, WA 98028, USA.
Integr Cancer Ther. 2013 Mar;12(2):126-35. doi: 10.1177/1534735412447582. Epub 2012 Jun 27.
Many women diagnosed with breast cancer receive both standard cancer treatment and care from providers trained in the emerging field of medicine called integrative oncology (IO) in which science-based complementary and alternative medical therapies are prescribed by physicians. The effectiveness of IO services has not been fully studied, so is yet unknown.
Determine if a matched, case-controlled prospective outcomes study evaluating the efficacy and safety of breast cancer IO care is feasible.
Methodological proof of principle requires demonstration that (1) it is possible to find matched control breast cancer patients using the Surveillance, Epidemiology and End
Results. A pilot study was conducted in 2008 (n = 14) to determine if matched controlled women could be identified in the western Washington SEER database. All 14 women who were approached agreed to participate. The cases were matched to the CSS along 5 variables: age and stage at diagnosis, race, and marital and Estrogen Receptors/Progesterone Receptors (ER/PR) status. Multiple matches were found for 12 of the 14 participants.
A prospective cohort study with a matched comparison group is a feasible and potentially rigorous
It may provide valuable data for the evaluation of the effectiveness of IO care on patient health, relapse rate, and health-related quality of life (HRQOL). A federally funded matched case controlled outcomes study is currently under way at Bastyr University and the Fred Hutchinson Cancer Research Center.
许多被诊断患有乳腺癌的女性同时接受标准的癌症治疗和来自整合肿瘤学(IO)领域的专业医生提供的治疗服务,后者是一门新兴学科,其中包括了基于科学的补充和替代医学疗法。IO 服务的有效性尚未得到充分研究,因此尚不清楚。
确定一项匹配、病例对照的前瞻性结局研究,评估乳腺癌 IO 护理的疗效和安全性是否可行。
方法学原理的证明需要证明(1)使用监测、流行病学和终期结果(SEER)数据库,找到匹配的对照乳腺癌患者是可能的;(2)招募的 IO 患者和他们的标准护理匹配患者在所有关键的基线特征上都是可比的;(3)能够收集足够的临床随访数据以评估患者的结局。
2008 年进行了一项试点研究(n=14),以确定是否可以在华盛顿西部 SEER 数据库中确定匹配的对照女性。所有被接触的女性都同意参与。这些病例根据 5 个变量与 CSS 相匹配:诊断时的年龄和分期、种族、婚姻状况以及雌激素受体/孕激素受体(ER/PR)状态。14 名参与者中有 12 名找到了多个匹配。
一项具有匹配对照组的前瞻性队列研究是可行的,并且具有潜在的严格性,它可能为评估 IO 护理对患者健康、复发率和健康相关生活质量(HRQOL)的有效性提供有价值的数据。目前,一项由联邦资助的、匹配病例对照的结局研究正在 Bastyr 大学和弗雷德·哈钦森癌症研究中心进行。