PD-1抑制剂联合化疗或安罗替尼治疗晚期非小细胞肺癌的临床疗效分析

    The clinical efficacy of PD-1 inhibitor combined with chemotherapy or anlotinib in the treatment of advanced non-small cell lung cancer

    • 摘要:
      目的: 探讨程序性死亡受体1(PD-1)抑制剂联合化疗或安罗替尼治疗晚期非小细胞肺癌的临床疗效。
      方法: 回顾性分析2020年12月至2022年12月收治的44例晚期非小细胞肺癌(NSCLC)病人的临床资料,根据治疗方案分为2组,A组和B组各22例。A组为PD-1抑制剂联合化疗药物;B组为PD-1抑制剂联合安罗替尼。比较2组临床疗效、生存情况及药物不良反应。
      结果: B组疾病控制率(DCR)为90.91%,明显高于A组的59.09%(P < 0.05),A、B 2组的无进展生存期(PFS)和总生存期(OS)差异均无统计学意义(P > 0.05)。治疗期间,B组血液毒性和胃肠道反应的不良反应发生率均低于A组(P < 0.05)。
      结论: PD-1抑制剂联合安罗替尼治疗晚期 NSCLC具有同PD-1抑制剂联合化疗相似的治疗效果,且不良反应明显减少。

       

      Abstract:
      Objective To investigate the clinical efficacy of programmed death receptor 1 (PD-1) inhibitor combined with chemotherapy or anlotinib in the treatment of advanced non-small cell lung cancer (NSCLC).
      Methods The clinical data of 44 patients with advanced non-small cell lung cancer from the First Affiliated Hospital of Bengbu Medical University from December 2020 to December 2022 were retrospectively analyzed. The patients were divided into the A group and B group (22 cases each group) according to the treatment regimen. The A group were treated with PD-1 inhibitor combined with chemotherapy drugs, and B group were treated with PD-1 inhibitor combined with anlotinib. The clinical efficacy, survival and adverse drug reactions were compared between two groups.
      Results The disease control rate (DCR) in the B group was 90.91%, which was significantly higher than that in A group (59.09%) (P < 0.05). There was no statistical significances in the progression-free survival (PFS) and overall survival (OS) between two groups (P > 0.05). During the treatment period, the incidence rates of adverse reactions (including the blood toxicity and gas trointestinal reactions) in B group were significantly less than those in A group (P < 0.05).
      Conclusions PD-1 inhibitor combined with antirotinib in the treatment of advanced NSCLC has a similar therapeutic effect as PD-1 inhibitor combined with chemotherapy, and the adverse reactions significantly reduce.

       

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