Cho Jin Sun, Seon Kieun, Kim Min-Yu, Kim Sang Wun, Yoo Young Chul
Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Anesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, South Korea.
Front Oncol. 2021 Nov 16;11:749003. doi: 10.3389/fonc.2021.749003. eCollection 2021.
Dexmedetomidine has sympatholytic, anti-inflammatory, and analgesic effects and may exert anti-tumor effect by acting on α2A adrenoreceptor. We investigated whether perioperative dexmedetomidine preserves immune function in patients undergoing uterine cancer surgery.
One hundred patients were randomly assigned to the control or dexmedetomidine groups (50 patients each). Dexmedetomidine was infused at rates of 0.4 μg/kg/h intraoperatively and 0.15 μg/kg/h during the first 24 h postoperatively. The primary outcome was natural killer (NK) cell activity, which was measured preoperatively and 1, 3, and 5 days postoperatively. The inflammatory response was measured by interleukin-6, interferon-γ, and neutrophil/lymphocyte ratio, and pain scores and opioid consumption were assessed. Cancer recurrence or metastasis and death were evaluated 2 years postoperatively.
NK cell activity decreased postoperatively in both groups and changes over time were not different between groups (=0.496). Interferon-γ increased postoperatively in the dexmedetomidine group, whereas it maintained at the baseline value in the control group. Change in interferon-γ differed significantly between groups (=0.003). Changes in interleukin-6 and neutrophil-lymphocyte ratio were comparable between groups. Both pain score with activity during the first 1 h and opioid consumption during the first 1-24 h postoperatively were lower in the dexmedetomidine group. Rates of cancer recurrence/metastasis (16.3% vs. 8.7%, =0.227) and death within 2 years postoperatively (6.7% vs. 2.2%, =0.318) were not different between groups.
Perioperative dexmedetomidine had no favorable impacts on NK cell activity, inflammatory responses, or prognosis, whereas it increased interferon-γ and reduced early postoperative pain severity and opioid consumption in uterine cancer surgery patients.
右美托咪定具有抗交感、抗炎和镇痛作用,可能通过作用于α2A肾上腺素能受体发挥抗肿瘤作用。我们研究了围手术期使用右美托咪定是否能保留子宫癌手术患者的免疫功能。
100例患者被随机分为对照组或右美托咪定组(每组50例)。术中以0.4μg/kg/h的速率输注右美托咪定,术后24小时内以0.15μg/kg/h的速率输注。主要结局指标是自然杀伤(NK)细胞活性,于术前、术后1天、3天和5天进行测量。通过白细胞介素-6、干扰素-γ和中性粒细胞/淋巴细胞比值来测量炎症反应,并评估疼痛评分和阿片类药物消耗量。术后2年评估癌症复发或转移及死亡情况。
两组术后NK细胞活性均降低,且两组随时间的变化无差异(P=0.496)。右美托咪定组术后干扰素-γ升高,而对照组维持在基线值。两组间干扰素-γ的变化有显著差异(P=0.003)。两组间白细胞介素-6和中性粒细胞-淋巴细胞比值的变化相当。右美托咪定组术后第1小时的疼痛评分及活动度和术后1-24小时的阿片类药物消耗量均较低。两组术后2年内癌症复发/转移率(16.3%对8.7%,P=0.227)和死亡率(6.7%对2.2%,P=0.318)无差异。
围手术期使用右美托咪定对NK细胞活性、炎症反应或预后无有利影响,而在子宫癌手术患者中可升高干扰素-γ并降低术后早期疼痛严重程度及阿片类药物消耗量。