Effects of Apatinib combined with Temozolomide on levels of sPD-1 and sPD-L1 in patients with drug-resistant recurrent glioblastoma

Clinics (Sao Paulo). 2024 May 10:79:100376. doi: 10.1016/j.clinsp.2024.100376. eCollection 2024.

Abstract

Objective: 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).

Study design: 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.

Results: 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).

Conclusions: 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.

Keywords: Apatinib; Glioblastoma; Recurrence; Soluble PD-1; Soluble PD-L1; Temozolomide.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • B7-H1 Antigen / analysis
  • Brain Neoplasms* / drug therapy
  • Drug Resistance, Neoplasm* / drug effects
  • Female
  • Glioblastoma* / drug therapy
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local* / drug therapy
  • Programmed Cell Death 1 Receptor* / antagonists & inhibitors
  • Pyridines* / therapeutic use
  • Temozolomide* / therapeutic use
  • Treatment Outcome

Substances

  • apatinib
  • Temozolomide
  • Pyridines
  • Programmed Cell Death 1 Receptor
  • B7-H1 Antigen
  • PDCD1 protein, human
  • CD274 protein, human