Efficacy and safety of brigatinib in ALK-positive non-small cell lung cancer treatment: A systematic review and meta-analysis

Abstract

BackgroundBrigatinib is a central nervous system-active second-generation anaplastic lymphoma kinase (ALK) inhibitor that targets a broad range of ALK rearrangements in patients with non-small cell lung cancer (NSCLC). The current study aimed to analyze the pooled effects and adverse events of brigatinib in patients with ALK-positive NSCLC.MethodsThe pooled estimates and 95% confidence intervals (CI) were calculated with DerSimonian-Laird method and the random effect model.ResultsThe pooled objective response rate (ORR) and disease control rate (DCR) of brigatinib were 64% (95% CI 45%-83%) and 88% (95% CI 80%-96%), respectively. The pooled mPFS was 10.52 months (95% CI 7.66-13.37). In the subgroup analyses by treatment line, the highest mPFS was reached in first-line treatment (24.00 months, 95% CI 18.40-43.20), followed by post-crizotinib second-line treatment (mPFS=16.26 months, 95% CI 12.87-19.65), and second-line with any prior ALK tyrosine kinase inhibitors (mPFS=12.96 months, 95% CI 11.14-14.78). Among patients with any baseline brain metastases, the pooled intracranial ORR (iORR) was estimated as 54% (95% CI 35%-73%) for any treatment line, and 60% (95% CI 39%-81%) for first-line treatment. Intracranial PFS (iPFS) reached 19.26 months (95% CI 14.82-23.70) in patients with any baseline brain metastases. Creatine phosphokinase (CPK) increased (44%, 95% CI 26%-63%), diarrhea (37%, 95% CI 27%-48%), and nausea (28%, 95% CI 17%-39%) of any grade were the most common adverse events.ConclusionBrigatinib is effective in the treatment of patients with ALK-positive NSCLC, particularly showing robust intracranial PFS. Brigatinib used as first-line treatment yielded superior PFS compared with brigatinib used as other treatment lines. These results suggested a benefit of using brigatinib earlier in the patient’s management. All adverse events are manageable, with CPK increased and gastrointestinal reactions found to be the most common types.Systematic Review Registrationhttps://inplasy.com/inplasy-2022-3-0142/, identifier (INPLASY202230141).

Nanosponges as an Emerging Platform for Cancer Treatment and Diagnosis

“…Brigatinib (BGT) is a tyrosine kinase inhibitor that has shown excellent activity against non‐small cell lung cancer. [ 125 ] In order to achieve a prolonged therapeutic effect, a recent study by Ahmed and teammates reported BGT‐loaded sustained‐release ethyl cellulose NSs for the treatment of non‐small cell lung cancer. [ 126 ] The developed BGT@NSs exhibited a particle size of 261.0 ± 3.5 nm (PDI: 0.301) along with a zeta potential of −19.83 ± 0.06 mV.…”