4.6 Article

The efficacy and safety of Apatinib in the treatment of advanced non-small cell lung cancer: A retrospective trial

Journal

FRONTIERS IN ONCOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.1030798

Keywords

advanced non-small cell lung cancer; anti-angiogenesis; apatinib; safety; survival

Categories

Funding

  1. National Natural Science Foundation of China
  2. Special Fund for Taishan Scholar Project
  3. Natural Science Foundation of Shandong Province Biomedicine Joint Fund
  4. [82172664]
  5. [81972850]
  6. [ts20190973]
  7. [ZR2021LSW020]

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The study retrospectively analyzed the treatment of Apatinib in 128 patients with advanced NSCLC, and the results showed that Apatinib at a lower dose (≤500mg/d) had good efficacy and safety in the treatment after first-line chemotherapy.
BackgroundAs a potent inhibitor of the vascular endothelial growth factor (VEGF) signaling pathway, Apatinib has been used in antitumor treatment for some time. The study aimed to research the therapeutic effects and toxicity of Apatinib in the treatment of advanced non-small cell lung cancer (NSCLC). MethodsWe retrospectively analyzed 128 NSCLC patients treated with Apatinib in Qilu Hospital of Shandong University. Response Evaluation Criteria in Solid Tumors (RECIST) criteria was adopted to evaluate the treatment effect, and Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 was conducted to determine the Adverse Events (AEs). Cox proportional hazard model and Kaplan-Meier function were applied to evaluate the progression-free survival (PFS) and overall survival (OS). ResultsAmong 128 NSCLC patients, partial response (PR) were observed in 15 patients, stable disease (SD) in 66 patients and progressive disease (PD) in 47 patients. The objective response rate (ORR) and disease control rate (DCR) accounted for 11.7% and 63.3% respectively. The median PFS (mPFS) and median OS (mOS) were 4.4 months and 17.2 months. Common side effects of Apatinib were hypertension (n=48), proteinuria (n=35), and hand-foot syndrome (HFS) (n=30), all of the side effects were controllable. No significant difference was observed in efficacy and AEs between the higher dose group (Apatinib>500mg/d) and the lower dose group (Apatinib=500mg/d). ConclusionsThe study suggested that Apatinib with a lower dose (=500mg/d) has good efficacy and safety in the treatment of advanced NSCLC after first-line chemotherapy.

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