Ren Baiqing, Cheng Muqiao, Liu Chao, Zheng Huiwen, Zhang Jingyue, Chen Wei, Song Jie, Zhuang Jingwen, Liu Tianya, Wang Rui, Wang Zhiping
Department of Anesthesiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Jiangsu Province Key Laboratory of Anesthesiology, Xuzhou Medical University, Xuzhou, China.
Front Oncol. 2023 Feb 24;13:1101449. doi: 10.3389/fonc.2023.1101449. eCollection 2023.
Neutrophil extracellular traps (NETs) can enhance the metastasis of non-small cell lung cancer (NSCLC). As biomarkers of tumor metastasis, metalloproteinases (MMPs) and vascular endothelial growth factor (VEGF) together with NETs are essential to endothelial-to-mesenchymal transition (EMT). We hypothesized that intravenous infusion of lidocaine and dexmedetomidine could reduce the production of NETs and biomarkers of tumor metastasis after video-assisted thoracic surgery (VATS) in NSCLC patients.
The trial included 132 NSCLC patients undergoing VATS. The patients were equally randomized to a placebo group (Group C), a lidocaine group (Group L, intravenous lidocaine 8 mg/kg/h for 15 minutes before anesthesia, 2 mg/kg/h during surgery, and 1 mg/kg/h until 24 hours after surgery), a dexmedetomidine group (Group D, intravenous dexmedetomidine 2 μg/kg/h for 15 minutes before anesthesia, 0.5 μg/kg/h during surgery, and 0.25 μg/kg/h until 24 hours after surgery), and a dexmedetomidine plus lidocaine group (Group LD, combination use of lidocaine and dexmedetomidine). The primary outcome was the production of myeloperoxidase (MPO) and citrullinated histone-3 (H3Cit), biomarkers of NETs, on postoperative day (POD) 1. MMP-3, MMP-9, and VEGF-α, as biomarkers of tumor metastasis, were also evaluated on POD 1.
The baseline patient characteristics and perioperative data did not differ between the study groups. MPO was significantly decreased in Groups L, D, and LD (-197.08 ± 34.01, -137.37 ± 32.41, and -189.45 ± 33.73 U/ml, <0.001, respectively) compared with Group C (-106.51 ± 25.44 U/ml). H3Cit was also lessened in Groups L, D, and LD (-49.51 ± 9.11, -34.80 ± 10.37, and -51.82 ± 8.98 ng/ml, <0.001, respectively) compared with Group C (-24.73 ± 7.65 ng/ml). Lidocaine and dexmedetomidine also reduced MMP-3 (-69.08 ± 13.22, -52.84 ± 13.78, -85.34 ± 12.59 -40.55 ± 10.71 ng/ml in Group L, D, LD Group C, <0.001, respectively), MMP-9 (-8.46 ± 1.68, -6.07 ± 1.82, -9.67 ± 1.43 -4.28 ± 1.29 ng/ml in Group L, D, LD Group C, P<0.001, respectively), and VEGF-α (-95.55 ± 22.53, -71.65 ± 18.77, -104.89 ± 15.49 -51.73 ± 16.27 pg/ml in Group L, D, LD Group C, P<0.001, respectively) on POD 1.
In NSCLC patients, continuous perioperative intravenous infusion of lidocaine and dexmedetomidine significantly reduced the production of NETs and tumor metastasis biomarkers on POD 1. Meanwhile, it also decreased inflammation, protected cellular immune function, reduced pain and opioid consumption, and improved the quality of postoperative recovery.
chictr.org.cn, identifier: 187049.
中性粒细胞胞外陷阱(NETs)可促进非小细胞肺癌(NSCLC)转移。作为肿瘤转移的生物标志物,金属蛋白酶(MMPs)和血管内皮生长因子(VEGF)与NETs共同在内皮-间质转化(EMT)中起重要作用。我们推测,静脉输注利多卡因和右美托咪定可减少NSCLC患者电视辅助胸腔手术(VATS)后NETs的产生及肿瘤转移生物标志物的生成。
该试验纳入了132例行VATS的NSCLC患者。患者被随机分为四组,每组人数相等:安慰剂组(C组)、利多卡因组(L组,麻醉前15分钟静脉输注利多卡因8mg/kg/h,术中2mg/kg/h,术后持续至24小时1mg/kg/h)、右美托咪定组(D组,麻醉前15分钟静脉输注右美托咪定2μg/kg/h,术中0.5μg/kg/h,术后持续至24小时0.25μg/kg/h)以及右美托咪定联合利多卡因组(LD组,联合使用利多卡因和右美托咪定)。主要观察指标为术后第1天(POD 1)NETs的生物标志物髓过氧化物酶(MPO)和瓜氨酸化组蛋白-3(H3Cit)的生成量。同时也评估了POD 1时作为肿瘤转移生物标志物的MMP-3、MMP-9和VEGF-α。
各研究组间患者的基线特征和围手术期数据无差异。与C组(-106.51±25.44 U/ml)相比,L组(-197.08±34.01 U/ml)、D组(-137.37±32.41 U/ml)和LD组(-189.45±33.73 U/ml)的MPO显著降低(P均<0.001)。与C组(-24.73±7.65 ng/ml)相比,L组(-49.51±9.11 ng/ml)、D组(-34.80±10.37 ng/ml)和LD组(-51.82±8.98 ng/ml)的H3Cit也减少(P均<0.001)。利多卡因和右美托咪定在POD 1时也降低了MMP-3(L组、D组、LD组分别为-69.08±13.22、-52.84±13.78、-85.34±12.59 ng/ml,C组为-40.55±10.71 ng/ml,P均<0.001)、MMP-9(L组、D组、LD组分别为-8.46±1.68、-6.07±1.82、-9.67±1.43 ng/ml,C组为-4.28±1.29 ng/ml,P均<0.001)和VEGF-α(L组、D组、LD组分别为-95.55±22.53、-71.65±18.77、-104.89±15.49 pg/ml,C组为-51.73±16.27 pg/ml,P均<0.001)。
在NSCLC患者中,围手术期持续静脉输注利多卡因和右美托咪定可显著降低POD 1时NETs及肿瘤转移生物标志物的生成。同时,它还减轻了炎症反应,保护了细胞免疫功能,减轻了疼痛并减少了阿片类药物的使用,改善了术后恢复质量。
chictr.org.cn,标识符:187049 。