Yan Juan, Xie Zheng-Zheng, Ma Na, Zheng Mao-Dong, Qiao Ting-Ting, Wang Yu
Juan Yan, Department of Pharmacy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei,075000, China.
Zheng-zheng Xie Department of Pharmacy, Beijing Shijitan Hospital, Beijing,100038, China.
Pak J Med Sci. 2023 Sep-Oct;39(5):1492-1495. doi: 10.12669/pjms.39.5.6772.
To investigate the effects of morphine hydrochloride sustained-release tablets and oxycodone hydrochloride sustained-release tablets on T-cell levels in advanced lung squamous cell carcinoma(LUSC) with moderate to severe cancer pain.
A retrospective study was used, ninety-eight patients who were admitted to The First Affiliated Hospital of Hebei North University for treatment of advanced LUSC with moderate to severe cancer pain between January 2021 and December 2021 were randomized into two groups(n=49 each) using the sealed envelope system. The reference group was treated with morphine hydrochloride sustained-release tablets, while the experimental group received oxycodone hydrochloride sustained-release tablets to compare pain relief rates(PRRs), levels of T cells, pain intensity, et al. Blood samples were collected for lymphocyte levels by flow cytometry.
The experimental group had significantly higher level than the reference group(<0.05). Before administration, the two groups did not differ greatly in levels of T-cell subsets or pain scores on the visual analog scale(>0.05, respectively). At 15 days of administration, the Treg level in the experimental group was higher than in the reference group; T helper 17 and 22 cells were reduced in both groups, and the decrease was more pronounced in the experimental group. At seven and 15 days of administration, the experimental group had a VAS score significantly lower than the reference group(<0.05). The total adverse reaction rate was significantly lower in the experimental group as compared with the reference group(<0.05).
Oxycodone hydrochloride sustained-release tablets demonstrate desirable efficacy and safety in advanced LUSC with moderate to severe cancer pain by modulating T-cells in the body and improving the PRR.
探讨盐酸吗啡缓释片和盐酸羟考酮缓释片对中重度癌痛的晚期肺鳞状细胞癌(LUSC)患者T细胞水平的影响。
采用回顾性研究,将2021年1月至2021年12月在河北北方学院附属第一医院收治的98例中重度癌痛的晚期LUSC患者,使用密封信封系统随机分为两组(每组n = 49)。参照组接受盐酸吗啡缓释片治疗,而试验组接受盐酸羟考酮缓释片治疗,以比较疼痛缓解率(PRR)、T细胞水平、疼痛强度等。通过流式细胞术采集血样检测淋巴细胞水平。
试验组水平显著高于参照组(<0.05)。给药前,两组T细胞亚群水平或视觉模拟量表疼痛评分差异不大(分别>0.05)。给药15天时,试验组调节性T细胞(Treg)水平高于参照组;两组辅助性T细胞17和22细胞均减少,且试验组减少更明显。给药7天和15天时,试验组视觉模拟量表(VAS)评分显著低于参照组(<0.05)。试验组总不良反应发生率显著低于参照组(<0.05)。
盐酸羟考酮缓释片通过调节体内T细胞并提高PRR,在中重度癌痛的晚期LUSC中显示出良好的疗效和安全性。