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Pyrotinib plus antiangiogenic agents for HER2-altered advanced non-small cell lung cancer: A retrospective real-world
Yaning Yang1, Guangjian Yang2, Weihua Li3
1Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Background:
Although some targeted therapies have been shown to be effective in treating HER2-altered non-small cell lung cancer (NSCLC), the survival demands have not yet been met due to the high cost and limited availability. This study aimed to assess the effectiveness and safety of pyrotinib plus antiangiogenic agents, including apatinib, anlotinib, and bevacizumab, in previously treated patients with HER2-altered advanced NSCLC.
Methods:
In this retrospective real-world study, patients with HER2-altered NSCLC who received pyrotinib plus antiangiogenic agents as a second- or later-line treatment between November 2015 and January 2022 were reviewed. The objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety profiles of patients were analyzed.
Results:
A total of 107 patients were included in the analysis, of which 59 patients (55.1%) had received at least two lines of prior chemotherapy or tyrosine kinase inhibitors. Most of them (87.9%) were identified as harboring HER2 exon 20 insertions. At the data cutoff date (May 13, 2022), the ORR, DCR, median PFS, and median OS were 19.6% (21/107), 94.4% (101/107), 7.13 months (95% confidence interval [CI]: 6.26-8.01), and 19.50 months (95% CI: 12.83-26.17), respectively. There was no difference in the PFS between patients receiving apatinib or anlotinib/bevacizumab (median PFS, 7.13 vs. 6.27 months, hazard ratio [HR] = 1.49, 95% CI: 0.87-2.54, p = 0.15). The most frequent grade 3 or higher treatment-related adverse events was diarrhea (17.6%), followed by hypertension (11.0%) and nausea (3.3%). No treatment-related death occurred.
Conclusion:
In this study, pyrotinib plus antiangiogenic agents demonstrated promising efficacy and were tolerable in HER2-altered NSCLC patients.
Insights
Pyrotinib combined with antiangiogenic agents shows promising effectiveness and tolerability in patients with HER2-altered non-small cell lung cancer (NSCLC). This combination therapy offers a viable treatment option for advanced NSCLC when other therapies are limited.
Area of Science:
- Oncology
- Pharmacology
- Clinical Medicine
Background:
- Targeted therapies for HER2-altered non-small cell lung cancer (NSCLC) show effectiveness but face challenges in cost and availability.
- There is a need for accessible and effective treatment options for patients with advanced HER2-altered NSCLC.
Purpose of the Study:
- To assess the efficacy and safety of pyrotinib plus antiangiogenic agents (apatinib, anlotinib, bevacizumab) in previously treated patients with HER2-altered advanced NSCLC.
- To evaluate real-world outcomes for this combination therapy in a patient cohort.
Main Methods:
- Retrospective analysis of 107 patients with HER2-altered NSCLC treated with pyrotinib plus antiangiogenic agents.
- Evaluation of objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety profiles.
- Patients received treatment as second- or later-line therapy between November 2015 and January 2022.
Main Results:
- The objective response rate (ORR) was 19.6% and the disease control rate (DCR) was 94.4%.
- Median progression-free survival (PFS) was 7.13 months and median overall survival (OS) was 19.50 months.
- The most common grade 3 or higher adverse events were diarrhea (17.6%) and hypertension (11.0%); no treatment-related deaths occurred.
Conclusions:
- Pyrotinib plus antiangiogenic agents demonstrate promising efficacy in HER2-altered NSCLC patients.
- This combination therapy is well-tolerated and represents a viable treatment option for previously treated patients.
- The findings support the use of pyrotinib and antiangiogenic agents in managing advanced HER2-altered NSCLC.
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