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An observational study of apatinib mesylate in treating advanced non-small cell lung cancer with unknown driving
Shaoshuang Fan1, Yuhuan Zou, Yifeng Wang
1Graduate School of North China, University of Science and Technology, Tangshan 063000, China.
Purpose:
To investigate the efficacy and safety of apatinib mesylate (AM) in treating advanced non-small cell lung cancer (aNSCLC) with wild or unknown epidermal growth factor receptor (w/nEGFR).
Methods:
A total of 34 w/nEGFR -aNSCLC patients who failed chemotherapy from August 2015 to April 2017 were administered orally AM (425 mg/d) as primary treatment and observed their progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR), as well as related adverse events.
Results:
Efficacy was evaluable in 30 cases, with median PFS (mPFS) 3.75 months (95% CI 0.648-6.852), ORR 20%, and DCR 73.33%. The main adverse reactions included hypertension (52.94%), hand-foot syndrome (52.94%), proteinuria (44.12%), and fatigue (41.18%); no drug-related death occurred. The efficacy correlation analysis showed that Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1 (p=0.008) combined with chemotherapy (p=0.009) were the factors that extended PFS, and combined chemotherapy (p=0.040, HR=3.052, 95% CI 1.052- 8.858) was an independent prognostic factor.
Conclusions:
AM has good therapeutic efficacy in treating aNSCLC patients after chemotherapy failure. The side effects can be controlled and it is worth testing it in large-scale clinical studies.
Insights
Apatinib mesylate shows good efficacy in advanced non-small cell lung cancer patients who failed chemotherapy. Side effects are manageable, warranting further large-scale clinical studies for this targeted therapy.
Area of Science:
- Oncology
- Pharmacology
Background:
- Advanced non-small cell lung cancer (aNSCLC) presents significant treatment challenges, particularly after failure of standard chemotherapy.
- Targeted therapies are crucial for improving outcomes in patients with wild or unknown epidermal growth factor receptor (w/nEGFR) mutations.
Purpose of the Study:
- To evaluate the efficacy and safety of apatinib mesylate (AM) as a treatment for advanced non-small cell lung cancer (aNSCLC) in patients with wild or unknown EGFR status.
- To assess progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR) of AM in this patient population.
Main Methods:
- A total of 34 patients with w/nEGFR-aNSCLC who had previously failed chemotherapy were enrolled.
- Patients received oral apatinib mesylate (425 mg/day) as primary treatment.
- Progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and adverse events were monitored.
Main Results:
- In 30 evaluable cases, the median PFS was 3.75 months, with an ORR of 20% and a DCR of 73.33%.
- Common adverse reactions included hypertension (52.94%), hand-foot syndrome (52.94%), proteinuria (44.12%), and fatigue (41.18%).
- ECOG performance status 0-1 and prior chemotherapy were identified as factors extending PFS, with combined chemotherapy being an independent prognostic factor.
Conclusions:
- Apatinib mesylate demonstrates good therapeutic efficacy in aNSCLC patients post-chemotherapy failure.
- The observed side effects are controllable, suggesting AM's potential as a treatment option.
- Further large-scale clinical studies are warranted to confirm these findings.
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