O'Neill Suzanne C, Vadaparampil Susan T, Street Richard L, Moore Tanina Foster, Isaacs Claudine, Han Hyo S, Augusto Bianca, Garcia Jennifer, Lopez Katherine, Brilleman Matilda, Jayasekera Jinani, Eggly Susan
Department of Oncology, Georgetown University, Washintgon DC, USA.
Department of Health Outcomes and Behavior, Moffitt Cancer Center, USA.
Patient Educ Couns. 2021 Feb;104(2):250-256. doi: 10.1016/j.pec.2020.08.037. Epub 2020 Sep 3.
Women with early-stage, ER + breast cancer are recommend to receive genomic profiling tests, such as the 21-gene Recurrence Score (RS) test, to guide treatment decisions. We examined test- and treatment-related information discussed and the associations between RS categories and aspects of communication during patient-oncologist clinical encounters.
As part of a larger trial, clinical encounters (N = 46) were audiorecorded and coded for 1) RS- and treatment-related information, 2) shared decision making, 3) patient active participation, and 4) oncologist patient-centered communication. We examined differences by RS category using mixed models, adjusting for nesting within oncologist.
Patients with a high RS were more likely to receive a chemotherapy recommendation (p < .01), hear about the risks/side effects of chemotherapy (p < .01), and offer their preferences (p = .02) than those with intermediate or low RS. Elements of shared decision making increased with RS. Oncologist patient-centered communication (M = 4.09/5, SD = .25) and patient active participation (M = 3.5/4, SD = 1.0) were high across RS.
Findings suggest that disease severity, rather than clinical uncertainty, impact treatment recommendations and shared decision making.
Oncologists adjust test- and treatment-related information and shared decision making by disease severity. This information provides a framework to inform decision making in complex cancer and genomics settings.
建议早期雌激素受体阳性(ER+)乳腺癌女性接受基因组分析检测,如21基因复发评分(RS)检测,以指导治疗决策。我们研究了患者与肿瘤学家临床会诊期间讨论的检测及治疗相关信息,以及RS类别与沟通各方面之间的关联。
作为一项更大规模试验的一部分,对临床会诊(N = 46)进行了录音,并针对以下方面进行编码:1)RS及治疗相关信息;2)共同决策;3)患者积极参与;4)肿瘤学家以患者为中心的沟通。我们使用混合模型按RS类别检查差异,并对肿瘤学家内部的嵌套情况进行了调整。
与RS中等或较低的患者相比,RS高的患者更有可能收到化疗建议(p < 0.01),了解化疗的风险/副作用(p < 0.01),并表达自己的偏好(p = 0.02)。共同决策的要素随着RS的增加而增加。肿瘤学家以患者为中心的沟通(M = 4.09/5,标准差 = 0.25)和患者积极参与(M = 3.5/4,标准差 = 1.0)在各RS水平上都较高。
研究结果表明,疾病严重程度而非临床不确定性会影响治疗建议和共同决策。
肿瘤学家根据疾病严重程度调整检测及治疗相关信息和共同决策。这些信息为复杂癌症和基因组学环境下的决策提供了一个框架。