Taselisib boosts breast tumour shrinkage

According to results of the LORELEI clinical trial, adding taselisib to letrozole before surgery significantly improved outcomes for patients with early breast cancer that was both estrogen receptor positive and HER2-negative (ER+/HER2-). 

“We were able to detect a reduction in tumour size after only 16 weeks of treatment, compared to patients who received letrozole plus placebo,” said study investigator Dr Cristina Saura, from Vall d’Hebron University Hospital in Barcelona, Spain. “Any decrease in tumour measurements is something positive for patients because this means the drug has had activity against their tumour in a short period of time.”

LORELEI is the first randomised study to demonstrate a significant increase in objective response rate (ORR) upon treatment with a PI3K selective inhibitor in this population of patients, noted the authors of the study, which was conducted at 85 sites across the world. 

“The alpha-specific story is important, because other PI3K inhibitors have had only a small effect, and the benefit-risk ratio was less favourable,” noted Prof Sibylle Loibl, Chair of the German Breast Group, who was not involved in the study but provided comment for ESMO. “In general, it is believed that alpha specific inhibitors will be more efficacious and less toxic than others”.

All of them had tissue analysed for PIK3CA mutant cancer cells and were randomised to receive letrozole plus either a placebo (n=168) or taselisib (n=166) for 16 weeks in order to shrink their tumour before surgery.

The study had two co-primary endpoints: one was ORR which was assessed by measuring the tumour size with magnetic resonance imaging; the second was the pathologic complete response (pCR) rate, which is a measure of the presence of cancer cells at the site after a tumour is surgically removed.

Among the 152 patients who had PIK3CA mutant cancer cells detected at baseline, taselisib worked particularly well, with 56.2% showing an ORR compared to 38% of patients who received placebo (odds ratio [OR] 2.03, 95%CI 1.06-3.88, p = 0.033).

“For me, the main message is that even though all patients seem to derive some benefit from taselisib, those who had this mutation seemed to derive more benefit,” said Dr Saura.

Discontinuation and reduced dosing of taselisib occurred in 10.8% and 11.4% of patients, respectively. The most common serious (grade 3 and 4) adverse events associated with the drug included gastrointestinal disorders (7.8%), infections (4.8%), skin / subcutaneous tissue disorders (4.8%), vascular disorders (3.6%), and metabolism and nutrition disorders (3.6%) including hyperglycemia (1.2%).

Although there was one sudden death in the taselisib-treated group, the study investigators considered it unrelated to the drug.

Prof Loibl concluded that “these are the first data indicating that the addition of an alpha-specific PI3K inhibitor might work in addition to an endocrine therapy in HER2-/Hr+ breast cancer. More data from LORELEI as well as data from the Phase III studies in metastatic breast cancer need to be awaited for evaluating the role of PIK3 Kinase inhibitors in breast cancer.”

The results of the study were presented at the ESMO 2017 Congress in Madrid.