Alectinib continuation beyond progression in ALK-positive non-small cell lung cancer with alectinib-refractory
Yimeng Li1, Zhanpeng Hao1, Yuyan Ma1
1Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Background:
Alectinib, a next-generation anaplastic lymphoma kinase tyrosine kinase inhibitor (ALK-TKI), has demonstrated noteworthy efficacy in the treatment of non-small cell lung cancer (NSCLC). Unfortunately, 53.3% of untreated patients receiving first-line treatment with alectinib developed resistance to alectinib. However, despite the widespread use of alectinib, studies on the efficacy and safety of continuing alectinib with other necessary therapies after progression of alectinib and possible population of benefit are still limited.
Methods:
This retrospective cohort study included fifteen patients with ALK-positive NSCLC from nine institutions in China who experienced disease progression after first- or second-line treatment and continued to receive alectinib treatment between 2019 and 2022. This study aimed to evaluate the median progression-free survival (mPFS), objective response rate (ORR), median overall survival (mOS), and adverse events (AEs) of continuing alectinib combined with other therapies after the emergence of drug resistance.
Results:
Among fifteen patients eligible for this study, all patients started continuing treatment with alectinib after oligoprogression or central nervous system (CNS) progression. The mPFS for the whole cohort receiving continuing alectinib with other necessary therapies was 8 months [95% confidence interval (CI): 4 to not applicable (NA)], with an ORR of 46.7%. The mOS was not reached. During continuing alectinib treatment, only one patient experienced grade 2 elevation of aspartate aminotransferase (AST) and serum glutamic-oxaloacetic transaminase (SGOT).
Conclusions:
The continuation of alectinib treatment combined with other necessary therapies demonstrates favorable response and safety in patients with ALK-positive NSCLC who experienced oligoprogression or CNS progression following alectinib in first- or second-line therapy. Instead of immediately switching to another ALK-TKI, continuing alectinib combined with other necessary therapies may offer greater survival benefits to the patients.
Insights
Continuing alectinib with other therapies shows promise for ALK-positive NSCLC patients who develop resistance. This approach may improve survival outcomes compared to switching treatments after disease progression.
Area of Science:
- Oncology
- Pharmacology
Background:
- Alectinib is a key treatment for anaplastic lymphoma kinase-positive non-small cell lung cancer (NSCLC).
- A significant percentage of patients develop resistance to alectinib, necessitating further treatment strategies.
- Limited data exists on continuing alectinib post-progression in NSCLC.
Purpose of the Study:
- To evaluate the efficacy and safety of continuing alectinib combined with other therapies after disease progression in ALK-positive NSCLC patients.
- To identify potential patient populations who may benefit from this strategy.
Main Methods:
- Retrospective cohort study of 15 patients with ALK-positive NSCLC in China (2019-2022).
- Patients received continued alectinib plus other therapies after oligoprogression or central nervous system (CNS) progression.
- Evaluated outcomes included median progression-free survival (mPFS), objective response rate (ORR), median overall survival (mOS), and adverse events (AEs).
Main Results:
- Continued alectinib treatment demonstrated a median PFS of 8 months (95% CI: 4 to NA).
- The objective response rate (ORR) was 46.7% in the studied cohort.
- Adverse events were minimal, with only one patient experiencing Grade 2 liver enzyme elevation.
Conclusions:
- Continuing alectinib with other therapies is effective and safe for ALK-positive NSCLC patients with oligoprogression or CNS progression.
- This strategy may offer superior survival benefits compared to immediate switching to alternative ALK-TKIs.
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