The Second Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, China; Department of Thoracic Medical Oncology, Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Hangzhou, China; Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, China.
Department of Thoracic Medical Oncology, Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Hangzhou, China; Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, China.
Ann Palliat Med. 2021 Jul;10(7):7841-7846. doi: 10.21037/apm-21-1400.
Neutropenia is the most common adverse reaction seen in small cell lung cancer after chemotherapy. Febrile neutropenia (FN) leads to an increase in hospitalizations and may even be life-threatening. This paper aims to investigate the efficacy and adverse reactions of mecapegfilgrastim in the primary prophylaxis of neutropenia in patients with small cell lung cancer after receiving intermediate risk chemotherapy with at least one patient risk factor.
The clinical records of 106 patients with small cell lung cancer admitted to Zhejiang Cancer Hospital from June 2019 to January 2021 were retrospectively analyzed. Patients were divided into a mecapegfilgrastim [pegylated recombinant human granulocyte colony stimulating factor (PEG-rhG-CSF)] group and control group, each with 53 patients. The mecapegfilgrastim group received subcutaneous injection of mecapegfilgrastim 24 hours after the first cycle of chemotherapy, while the control group did not receive this. The Chi-square (χ2) test or Fisher exact test were used to compare the incidence of neutropenia, FN, and the proportion of patients administrated with full dose chemotherapy in the two groups after the first cycle of chemotherapy. Data on adverse events after mecapegfilgrastim were also collected.
After the first cycle of chemotherapy, the incidence of neutropenia in the mecapegfilgrastim group was significantly lower than that in the control group (P=0.001) and the incidence of FN in the mecapegfilgrastim group was lower than that in the control group (P=0.118). The proportion of patients administrated with full-dose chemotherapy in the mecapegfilgrastim group was significantly higher than that in the control group (P=0.001). The main adverse reactions to mecapegfilgrastim were muscle pain, fever, and fatigue.
After receiving intermediate risk chemotherapy, the incidence of neutropenia was significantly reduced by the primary prophylaxis of mecapegfilgrastim in patients with small cell lung cancer. The adverse events of mecapegfilgrastim were mild and tolerable, and included muscle pain, fever, and fatigue.
中性粒细胞减少是小细胞肺癌化疗后最常见的不良反应。发热性中性粒细胞减少症(FN)会导致住院率增加,甚至可能危及生命。本文旨在研究至少有一个患者危险因素的小细胞肺癌患者接受中危化疗后,预防性使用美柏格司亭(PEG-rhG-CSF)预防中性粒细胞减少的疗效和不良反应。
回顾性分析 2019 年 6 月至 2021 年 1 月浙江肿瘤医院收治的 106 例小细胞肺癌患者的临床资料。患者分为美柏格司亭[聚乙二醇化重组人粒细胞集落刺激因子(PEG-rhG-CSF)]组和对照组,每组 53 例。美柏格司亭组在化疗第 1 周期后 24 小时内皮下注射美柏格司亭,对照组不使用。化疗第 1 周期后,比较两组中性粒细胞减少、FN 发生率及全剂量化疗患者比例。还收集了美柏格司亭后不良事件的数据。
化疗第 1 周期后,美柏格司亭组中性粒细胞减少发生率明显低于对照组(P=0.001),FN 发生率低于对照组(P=0.118)。美柏格司亭组全剂量化疗患者比例明显高于对照组(P=0.001)。美柏格司亭的主要不良反应为肌肉疼痛、发热和疲劳。
小细胞肺癌患者接受中危化疗后,预防性使用美柏格司亭可显著降低中性粒细胞减少的发生率。美柏格司亭的不良反应轻微且可耐受,包括肌肉疼痛、发热和疲劳。