Department of Human Sciences, The Ohio State University, Columbus, OH, 43210, USA.
Yale School of Medicine, Center for Breast Cancer, New Haven, CT, 06511, USA.
Breast Cancer Res Treat. 2024 Dec;208(3):605-617. doi: 10.1007/s10549-024-07457-w. Epub 2024 Aug 14.
Minocycline suppresses chemotherapy-induced neuroinflammation in preclinical models, but its effects in cancer survivors are unknown. This study evaluated the longitudinal effects of minocycline on affective behaviors, cognitive functions, and inflammation in women with breast cancer (BC) undergoing chemotherapy.
This is a pilot, double-blind, randomized controlled trial of oral minocycline (100 mg BID) versus placebo for chemotherapy-induced affective disorders in women initiating chemotherapy for stage I-III BC. Participants received minocycline or placebo up to one week before chemotherapy, continuing through cycle 4 (C4). Epidemiologic Studies Depression Scale (CES-D) and State-Trait Anxiety Inventory (STAI) were assessed at baseline, each cycle of chemotherapy (C1-C4), 2-3-week post-chemotherapy (end of chemotherapy), and 6-month post-chemotherapy (6 M) as the primary outcomes. Sub-group analysis of CES-D and STAI based on the severity of symptoms was also performed. Changes in self-reported cognition and serum inflammatory markers were also evaluated.
Fifty-seven women enrolled and 55 completed the study. Except for Interleukin-8 (p ≤ 0.03), changes in inflammatory markers, cognitive function, CES-D, and STAI were not significantly different between groups from baseline to any cycle or post-chemotherapy time point (all p > 0.05), adjusting for baseline scores. Increases in serum Interleukin-8 from baseline to C4 and 6 M were ameliorated by minocycline (p < 0.05). The sub-group symptomatic for depression (CES-D > = 16 at baseline) treated with minocycline had a greater reduction in CES-D score compared to placebo from baseline to 6 M (p = 0.01).
Despite attenuation of IL-8, minocycline did not alter self-reported affective symptoms or cognition in this cohort of BC survivors undergoing chemotherapy. The effect of minocycline on BC survivors symptomatic for depression before chemotherapy warrants further investigation.
米诺环素可抑制临床前模型中的化疗诱导性神经炎症,但它在癌症幸存者中的作用尚不清楚。本研究评估了米诺环素对接受化疗的乳腺癌(BC)女性的情感行为、认知功能和炎症的纵向影响。
这是一项针对口服米诺环素(100mg,bid)与安慰剂在接受 I-III 期 BC 化疗的女性中治疗化疗诱导的情感障碍的先导性、双盲、随机对照试验。参与者在化疗前一周内接受米诺环素或安慰剂,持续至第 4 周期(C4)。在基线、每个化疗周期(C1-C4)、化疗结束后 2-3 周(结束时)和化疗后 6 个月(6M)时评估流行病学研究抑郁量表(CES-D)和状态-特质焦虑量表(STAI),作为主要结局。还对 CES-D 和 STAI 基于症状严重程度进行了亚组分析。还评估了自我报告认知和血清炎症标志物的变化。
57 名女性入组,55 名完成研究。除白细胞介素-8(p≤0.03)外,从基线到任何周期或化疗后时间点,炎症标志物、认知功能、CES-D 和 STAI 的变化在组间无显著差异(所有 p>0.05),调整了基线评分。与安慰剂相比,米诺环素可改善从基线到 C4 和 6M 的血清白细胞介素-8 的增加(p<0.05)。在基线时 CES-D>16 的亚组中,与安慰剂相比,米诺环素治疗组的 CES-D 评分从基线到 6M 时下降更大(p=0.01)。
尽管白细胞介素-8 减少,但米诺环素并未改变接受化疗的 BC 幸存者自我报告的情感症状或认知。米诺环素对化疗前有抑郁症状的 BC 幸存者的影响需要进一步研究。