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Safety and efficacy of anlotinib hydrochloride capsules in advanced non-small-cell lung cancer: a multicenter, real-world study

    Meng Wang‡

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    ‡These two authors contributed equally

    Search for more papers by this author

    ,
    Mengxia Mao‡

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    ‡These two authors contributed equally

    Search for more papers by this author

    ,
    Yonghua Yang

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    ,
    Zhiqiang Cai

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    ,
    Yan Li

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    ,
    Yuanyuan Chen

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    ,
    Jun Cai

    *Author for correspondence:

    E-mail Address: caijun0540@163.com

    Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    &
    Qingqing Ye

    **Author for correspondence:

    E-mail Address: zhiyin0540@163.com

    Department of Breast Surgery, The First Affiliated Hospital of Yangtze University, Jingzhou City, Hubei Province, China, 434000

    Published Online:https://doi.org/10.2217/fon-2023-0470

    Objective: To investigate the safety and efficacy of anlotinib hydrochloride capsules in stage III–IV non-small-cell lung cancer (NSCLC). Methods: NSCLC patients received anlotinib monotherapy or combination therapy. The primary end point was adverse reactions during anlotinib treatment and the secondary end point was progression-free survival. Results: During anlotinib treatement, 41.85% (167/399) of patients experienced adverse reactions, and the monotherapy group had a lower incidence than the combination group (36.89 vs 49.68%; p = 0.012). The median progression-free survival of patients in the monotherapy group was significantly lower than that in the combination group (5 vs 6 months; p = 0.0119). Conclusion: Compared with anlotinib monotherapy, combination therapy resulted in longer PFS and a higher incidence of adverse reactions in patients with NSCLC.

    Papers of special note have been highlighted as: • of interest; •• of considerable interest

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