AKT inhibitor biomarkers remain undefined in metastatic breast cancer (MBC). The phase Ib TAKTIC trial evaluated ipatasertib with endocrine therapy, or with fulvestrant plus palbociclib, in endocrine-resistant HR + /HER2- MBC. Exploratory baseline ± post-progression circulating-tumor DNA (ctDNA) was analyzed for genomic alterations associated with outcomes. Progression-free survival (PFS) was assessed using Kaplan-Meier and Cox modeling. McNemar’s test compared acquired alterations in paired samples. Combinatorial effects were explored in patient-derived cell lines treated with ipatasertib and palbociclib. Forty-seven patients received doublet ( n = 21) or triplet ( n = 26) therapy, and 87% had prior CDK4/6 inhibitor exposure. Median PFS was 5.72 months. PI3K pathway alterations ( PIK3CA/AKT1/PTEN ) correlated with longer PFS on triplet therapy (15.66 vs 5.57 months, HR 0.38, 95% CI 0.15–0.93) but not in the doublet group or overall cohort. FGFR1 amplifications (13%) trended toward poorer PFS (3.64 vs 6.96 months, HR 2.36, 95% CI 0.91–5.24), and EGFR amplifications (9%) correlated with shorter PFS (2.97 vs 6.96 months, HR 4.26, 95% CI 1.31–11.21). ESR1 mutations (30%) were associated with worse PFS (3.36 vs 7.29 months, HR 2.33, 95% CI 1.18–4.41). Paired ctDNA from 31 patients demonstrated emergent FGFR1, EGFR , and ESR1 alterations at progression, each occurring in 10–13% of cases. Ipatasertib with palbociclib had greater efficacy in PIK3CA- mutant than wild-type cell lines. Overall, ctDNA biomarkers correlated with PFS on ipatasertib-based therapy, and predictive versus prognostic significance requires validation.
No takes yet. Share an insight, caveat, or question.
Lloyd et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: