Department of Neurosurgery, Affiliated Hospital of North Sichuan Medical College, Nanchong City, Sichuan Province, China.
Department of Orthopedics and Cosmetology, Affiliated Hospital of North Sichuan Medical College, Nanchong City, Sichuan Province, China.
Clinics (Sao Paulo). 2024 May 10;79:100376. doi: 10.1016/j.clinsp.2024.100376. eCollection 2024.
This study aimed to explore the effects of Apatinib combined with Temozolomide (TMZ) on the levels of Soluble PD-1 (sPD-1) and Soluble Programmed Death-1 Ligand (sPD-L1) in patients with drug-resistant recurrent Glioblastoma (GB).
A total of 69 patients with recurrent GB from September 2020 to March 2022 were recruited and assigned to the control group (n = 34) and observation group (n = 35) according to different treatment options after tumor recurrence. The control group was treated with TMZ, and the observation group was treated with Apatinib combined with TMZ. Levels of sPD-1 and spd-l1, clinical efficacy, survival time and adverse reactions were observed and compared between the two groups.
General data including gender, age, body mass index, and combined diseases indicated no statistical significance between groups (p > 0.05). Before the intervention, sPD-1 and sPD-L1 levels were not significantly different in the two groups (p > 0.05). After interventions, levels of PD-1 and sPD-L1 levels decreased significantly (p < 0.05). The objective remission rate and clinical benefit rate of the observation group were higher and overall survival and progression-free survival were longer than those of the control group (p < 0.05). No significant difference was observed in major adverse reactions among patients (p > 0.05).
Apatinib combined with TMZ is safe and effective in the treatment of recurrent GB. The combined application of the two can reduce the levels of sPD-1 and sPD-L1, which has important clinical application value.
本研究旨在探讨阿帕替尼联合替莫唑胺(TMZ)治疗耐药性复发性胶质母细胞瘤(GB)患者对可溶性程序性死亡受体-1(sPD-1)和可溶性程序性死亡配体-1(sPD-L1)水平的影响。
共纳入 2020 年 9 月至 2022 年 3 月期间 69 例复发性 GB 患者,根据肿瘤复发后的不同治疗方案分为对照组(n=34)和观察组(n=35)。对照组采用 TMZ 治疗,观察组采用阿帕替尼联合 TMZ 治疗。观察并比较两组患者的 sPD-1、sPD-L1 水平、临床疗效、生存时间及不良反应。
两组患者的性别、年龄、体质量指数、合并疾病等一般资料比较差异无统计学意义(p>0.05)。干预前,两组 sPD-1、sPD-L1 水平比较差异无统计学意义(p>0.05)。干预后,两组患者 sPD-1、sPD-L1 水平均显著降低(p<0.05)。观察组客观缓解率和临床获益率均高于对照组,总生存时间和无进展生存时间均长于对照组(p<0.05)。两组患者主要不良反应发生率比较差异无统计学意义(p>0.05)。
阿帕替尼联合 TMZ 治疗复发性 GB 安全有效,两药联合应用可降低 sPD-1、sPD-L1 水平,具有重要的临床应用价值。