First-line ipatasertib-paclitaxel combo fails to show PFS benefit in PIK3CA/AKT1/PTEN-altered aTNBC

Roshini Claire Anthony
03 Feb 2021
First-line ipatasertib-paclitaxel fails to show PFS benefit in PIK3CA/AKT1/PTEN-altered aTNBC

Ipatasertib plus paclitaxel in the first-line setting does not confer a progression-free survival (PFS) benefit to patients with PIK3CA/AKT1/PTEN-altered locally advanced unresectable or metastatic triple-negative breast cancer (aTNBC), according to a study presented at SABCS 2020.

Participants in Cohort A of the phase III double-blind IPATunity130 trial were 255 patients with PIK3CA/AKT1/PTEN-altered aTNBC with no previous chemotherapy exposure for aTNBC* and ECOG performance status 0/1. They were randomized 2:1 to receive oral ipatasertib (400 mg QD) or placebo on days 1–21 plus intravenous paclitaxel (80 mg/m2 on days 1, 8, and 15), with cycles repeated every 28 days.

Fifty-one percent of patients had PIK3CA/AKT1-activating mutations, while 49 percent had PTEN alterations (without PIK3CA/AKT1-activating mutations). Fifty-nine percent of patients had visceral disease and 51 percent had received neoadjuvant chemotherapy. Mean duration of paclitaxel treatment was comparable between the ipatasertib and placebo groups (mean 5.5 vs 5.4 months). Thirty-three percent of patients were still undergoing treatment at data cut-off.

After a median 8.3 months of follow-up, PFS did not significantly differ between patients who received ipatasertib-paclitaxel and placebo-paclitaxel (median 7.4 vs 6.1 months; hazard ratio [HR], 1.02, 95 percent confidence interval, 0.71–1.45; p=0.9237). [SABCS 2020, abstract GS3-04]

Overall survival was still immature at data cut-off.

Confirmed overall response rate was also comparable between the ipatasertib and placebo arms (39 percent vs 35 percent), as was clinical benefit rate (objective response or stable disease 24 weeks; 47 percent vs 45 percent).

Incidence of grade 3 adverse events (AEs) was comparable between ipatasertib and placebo recipients (46 percent vs 44 percent), as was serious AE (19 percent vs 21 percent) and fatal AE (1 percent each) incidence.

AEs more frequently led to dose reduction of any treatment in the ipatasertib compared with the placebo group (35 percent vs 14 percent). However, AE-related treatment discontinuation was comparable between groups (14 percent vs 15 percent). The most frequently occurring AEs were diarrhoea (80 percent vs 31 percent), alopecia (46 percent vs 44 percent), and nausea (36 percent vs 23 percent), with grade 3 diarrhoea occurring in 9 and 2 percent of ipatasertib and placebo recipients, respectively.

The phase II LOTUS trial showed that the first-line combination of ipatasertib and paclitaxel increased PFS compared with paclitaxel alone in an unselected population of patients with aTNBC (median 6.2 vs 4.9 months; HR, 0.60), said Associate Professor Rebecca Dent from the National Cancer Centre Singapore who presented the findings.

This effect was more pronounced in patients with PIK3CA/AKT1/PTEN alterations (median 9.0 vs 4.9 months; HRunstratified, 0.44), she said.

Results from this trial differ from findings of the randomized phase II trials of AKT inhibition in aTNBC, ie, the LOTUS trial which assessed the combination of paclitaxel and ipatasertib and the PAKT trial which assessed paclitaxel plus capivasertib, noted Dent.

There was no subgroup that appeared to benefit from this treatment except for patients with PD-L1–positive disease. However, due to the small sample size, this finding warrants assessment in larger trials, said Dent.

“Further analyses of IPATunity130 Cohort A are ongoing to explore potential biomarkers of benefit from ipatasertib,” she concluded.


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