Neurocognitive Research Lab, Department of Psychiatry and Behavioral Sciences, Memorial Sloan Kettering Cancer Center, 641 Lexington Avenue, 7th Floor, New York, NY, USA.
Departments of Psychiatry and Anesthesiology, Weill Medical College of Cornell University, New York, NY, USA.
Breast Cancer Res Treat. 2022 Jul;194(2):413-422. doi: 10.1007/s10549-022-06623-2. Epub 2022 May 19.
Tumor features associated with aggressive cancers may affect cognition prior to systemic therapy. We evaluated associations of cognition prior to adjuvant therapy and tumor aggressivity in older breast cancer patients.
Women diagnosed with non-metastatic breast cancer (n = 705) ages 60-98 were enrolled from August 2010-March 2020. Cognition was measured post-surgery, pre-systemic therapy using self-reported (FACT-Cog Perceived Cognitive Impairment [PCI]) and objective tests of attention, processing speed, and executive function (APE domain) and learning and memory [LM domain]. Linear regression tested associations of pre-treatment tumor features and cognition, adjusting for age, race, and study site. HER2 positivity and higher stage (II/III vs. 0/I) were a priori predictors of cognition; in secondary analyses we explored associations of other tumor features and cognitive impairment (i.e., PCI score < 54 or having 2 tests < 1.5 SD or 1 test < 2 SD from the mean APE or LM domain score).
HER2 positivity and the hormone receptor negative/HER2 + molecular subtype were associated with lower adjusted mean self-reported cognition scores and higher impairment rates (p values < .05). Higher stage of disease was associated with lower objective performance in APE. Other tumor features were associated with cognition in unadjusted and adjusted models, including larger tumor size and lower PCI scores (p = 0.02). Tumor features were not related to LM.
Pre-adjuvant therapy cognition was associated with HER2 positivity and higher stage of disease and other features of aggressive tumors. Additional research is needed to confirm these results and assess potential mechanisms and clinical management strategies.
与侵袭性癌症相关的肿瘤特征可能会在全身治疗之前影响认知。我们评估了老年乳腺癌患者辅助治疗前认知与肿瘤侵袭性的相关性。
2010 年 8 月至 2020 年 3 月,从诊断为非转移性乳腺癌(n=705)的年龄在 60-98 岁的女性中招募了患者。在接受手术和全身治疗之前,使用自我报告的(FACT-Cog 感知认知障碍[PCI])和注意力、处理速度和执行功能(APE 域)以及学习和记忆[LM 域]的客观测试来测量认知。线性回归检验了治疗前肿瘤特征与认知的相关性,调整了年龄、种族和研究地点。HER2 阳性和较高的分期(II/III 期与 0/I 期)是认知的先验预测因子;在二次分析中,我们探讨了其他肿瘤特征与认知障碍(即 PCI 评分<54 分或有 2 项测试<1.5 个标准差或 1 项测试<2 个标准差的 APE 或 LM 域评分)的相关性。
HER2 阳性和激素受体阴性/HER2+分子亚型与调整后的自我报告认知评分较低和较高的损伤率相关(p 值<0.05)。疾病的较高分期与 APE 中的较低客观表现相关。其他肿瘤特征在未调整和调整模型中与认知相关,包括较大的肿瘤大小和较低的 PCI 评分(p=0.02)。肿瘤特征与 LM 无关。
辅助治疗前的认知与 HER2 阳性和疾病的较高分期以及其他侵袭性肿瘤特征有关。需要进一步研究来证实这些结果,并评估潜在的机制和临床管理策略。