Overall survival was not improved with alectinib in patients with treatment-naïve, advanced ALK-positive non-small cell lung cancer, compared to crizotinib.
Overall survival (OS) was not improved with alectinib (Alecensa) in patients with treatment-naïve, advanced ALK-positive non-small cell lung cancer (NSCLC), compared to crizotinib (Xalkori).
However, the data, which were presented during the 2021 ASCO Annual Meeting, may be confounded since 78.8% of patients who received crizotinib received alectinib initially.
In the primary analysis of the phase 3 randomized, open-label J-ALEX (JapicCTI-132316) study, alectinib demonstrated better progression-free survival (PFS) than crizotinib (HR = 0.34, 99.7% CI, 0.17-0.71; P = .0001). Median PFS was not reached with alectinib, compared to 10.2 months with crizotinib. Additional data from a data cut-off in June 2018 continued demonstrating better PFS for alectinib than crizotinib (HR = 0.37; 95% CI, 0.26-0.52). In the final analysis, investigators sought to examine OS data after a minimum of 5 years of follow up.
“In this final analysis, from J-ALEX, prolongation of OS in the alectinib arm was not observed compared to crizotinib,” said Hiroshige Yoshioka, MD, of Kansaid Medical University Hospital, in a presentation of the findings. “However, median OS was not reached in either treatment arm. This OS result may have been confounded by crossover.”
Patients were randomized 1:1 to receive either alectinib (300 mg twice daily) or crizotinib (250mg twice daily) until progressive disease (PD), unacceptable toxicity, withdrawal or death. Treatment crossover between arms was permitted after withdrawal.
Patients were eligible for the study if they were 20 years of age or older, had stage 3B, 4 or recurrent NSCLC, had ALK-positive disease, an ECOG score of 0-2, had ≥ 1 measurable lesion assessed by investigator and had received 1 or less prior chemotherapy. Treated or asymptomatic brain metastases were allowed.
At a median follow-up of 68.6 months in the alectinib arm and 68 months in the crizotinib arm, deaths occurred in 40.8% and 39.4% of patients, respectively. Five-year survival rates for alectinib-treated patients were 60.85% compared to 64.11% in crizotinib-treated patients.
The global ALEX study, in which no major subsequent ALK TKIs as opposed to the J-ALEX study, including treatment crossover, demonstrated clinically meaningful OS improvement from alectinib compared to crizotinib in treatment-naïve, advanced ALK-positive NSCLC. OS data remain immature (HR = 0.67; 95% CI 0.46-0.98).