小细胞肺癌患者放化疗联合安罗替尼治疗后预后影响因素分析
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郑州大学附属郑州中心医院放疗科

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    摘要:

    目的:探讨小细胞肺癌(Small Cell Lung Cancer,SCLC)患者接受放化疗联合安罗替尼治疗的预后影响因素,为优化临床治疗策略提供依据。方法:选取2021年1月至2024年1月期间郑州市中心医院和郑州市中心医院新郑分院(新郑市公立人民医院)收治的小细胞肺癌患者64例作为研究对象。所有患者均接受过放化疗(依托泊苷+铂类+胸部放疗)联合安罗替尼治疗。收集患者的基线资料;统计患者治疗后的预后情况。采用Kaplan-Meier法分析无进展生存期(Progression-free surviva,PFS)和总生存期(Overall survival,OS)。Cox回归模型对影响患者预后的单因素及多因素进行分析。结果:全组中位PFS为7.65个月(95%CI: 6.42-8.88),中位OS为14.80个月(95%CI: 12.76-16.84)。单因素分析显示,美国东部肿瘤协作组(Eastern Cooperative Oncology Group,ECOG)评分≥2分(P=0.007)、广泛期(P=0.003)、脑转移(P=0.011)、神经元特异性烯醇化酶(Neuron-specific enolase,NSE)≥35 ng/mL(P=0.002)、NLR≥3.5(P=0.018)、安罗替尼治疗<4周期(P<0.001)及疗效非PR/CR(P<0.001)与较差预后相关。多因素分析证实,ECOG评分≥2分(HR=2.04,P=0.010)、广泛期(HR=2.15,P=0.009)、脑转移(HR=1.85,P=0.027)、NSE≥35 ng/mL(HR=2.30,P=0.003)、中性粒细胞/淋巴细胞比 (Neutrophil/lymphocyte ratio,NLR)≥3.5(HR=1.78,P=0.042)、安罗替尼治疗<4周期(HR=3.05,P<0.001)及疗效非PR/CR(HR=2.47,P=0.002)为OS的独立危险因素。结论:ECOG评分、临床分期、脑转移、NSE水平、NLR、安罗替尼治疗周期及疗效是SCLC患者放化疗联合安罗替尼治疗预后的关键影响因素。

    Abstract:

    Objective: To explore the prognostic factors of patients with Small Cell Lung Cancer (SCLC) treated with radiotherapy, chemotherapy combined with anlotinib, and to provide a basis for optimizing clinical treatment strategies. Methods: Sixty-four patients with small cell lung cancer admitted to Zhengzhou Central Hospital and Xinzheng Branch of Zhengzhou Central Hospital (Xinzheng Public People"s Hospital) from January 2021 to January 2024 were selected as the research subjects. All patients received radiotherapy and chemotherapy (etoposide + platinum + thoracic radiotherapy) combined with anlotinib treatment. Collect the baseline data of the patients; Statistically analyze the prognosis of the patients after treatment. The Progression-free survival (PFS) and Overall survival (OS) were analyzed by the Kaplan-Meier method. The Cox regression model was used to analyze the univariate and multivariate factors influencing the prognosis of patients. Results: The median PFS of the entire group was 7.65 months (95%CI: 6.42-8.88), and the median OS was 14.80 months (95%CI: 12.76-16.84). Univariate analysis showed that the Eastern Cooperative Oncology Group of the United States ECOG score ≥2 points (P=0.007), extensive stage (P=0.003), brain metastasis (P=0.011), Neuron-specific enolase (Neuron-specific enolase) NSE ≥35 ng/mL (P=0.002), NLR≥3.5 (P=0.018), anlotinib treatment <4 cycles (P<0.001), and non-PR /CR of therapeutic effect (P<0.001) were associated with a poorer prognosis. Multivariate analysis confirmed that ECOG score ≥2 points (HR=2.04, P=0.010), extensive stage (HR=2.15, P=0.009), brain metastasis (HR=1.85, P=0.027), and NSE≥35 ng/mL (HR=2.30) P=0.003), Neutrophil/lymphocyte ratio (NLR) ≥3.5 (HR=1.78, P=0.042), anlotinib treatment <4 cycles (HR=3.05) (P<0.001) and therapeutic effect non-PR /CR (HR=2.47, P=0.002) were independent risk factors for OS. Conclusion: ECOG score, clinical stage, brain metastasis, NSE level, NLR, anlotinib treatment cycle and efficacy are the key influencing factors for the prognosis of SCLC patients with radiotherapy and chemotherapy combined with anlotinib.

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  • 收稿日期:2025-05-21
  • 最后修改日期:2025-06-11
  • 录用日期:2025-06-20
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