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Kisqali approved by FDA in combination with an aromatase inhibitor for the frontline treatment of postmenopausal women with HR–positive, HER2-negative advanced breast cancer


The CDK 4/6 inhibitor Ribociclib ( Kisqali ) has been approved by the FDA ( Food and Drug Administration ) for use in combination with an aromatase inhibitor for the frontline treatment of postmenopausal women with hormone-receptor (HR)–positive, HER2-negative advanced breast cancer.

The approval is based on findings from the phase III MONALEESA-2 trial, in which combining Ribociclib with Letrozole reduced the risk of progression or death by 44% compared with Letrozole alone in the first-line setting for HR+/HER2- advanced breast cancer ( hazard ratio, HR=0.556; 95% CI, 0.43-0.72; P less than 0.0001 ).

In the MONALEESA-2 trial, Ribociclib plus Letrozole has reduced the risk of disease progression or death by 44% over Letrozole alone, and more than half of patients ( 53% ) with measurable disease taking Ribociclib plus Letrozole experienced a tumor burden reduction of at least 30%.
These results affirm that combination therapy with a CDK 4/6 inhibitor like Ribociclib and an aromatase inhibitor should be a new standard of care for initial treatment of HR+ advanced breast cancer.

The phase III MONALEESA-2 trial enrolled 668 postmenopausal women with advanced breast cancer who had not yet received prior therapy for advanced disease. Letrozole was administered at 2.5 mg per day along with placebo or Ribociclib at 600 mg per day for 3 weeks followed by 1 week off.
The primary endpoint of the study was progression-free survival ( PFS ). Secondary outcome measures focused on overall survival, overall response rates, and safety.

The trial ended prematurely after an initial interim data analysis demonstrated a significant benefit in favor of the Ribociclib arm. The analysis occurred after 243 qualifying events, including progression or death. Ninety-three ( 27.8% of randomized patients ) events occurred in the Ribociclib arm compared with 150 ( 44.7% ) in the placebo arm.

At a median follow-up of 15.3 months, the Ribociclib group’s median progression-free survival had yet to be reached, whereas the placebo group had an estimated median PFS of 14.7 months.
Blinded PFS assessment by an independent review committee resulted in a hazard ratio of 0.59 in favor of the Ribociclib arm ( P=0.002 ).

After an additional 11 months of follow-up, a subsequent analysis showed that the median PFS was 25.3 months with the Ribociclib combination versus 16 months with Letrozole alone. Overall survival data are still not mature.

The 18-month progression-free survival was 63% with Ribociclib versus 42.2% for the placebo group. Among patients with measurable disease, the overall response rate was 52.7% with Letrozole plus Ribociclib and 37.1% with Letrozole and placebo.

Ribociclib did add to treatment-associated toxicity, as 59.3% of patients who received the CDK 4/6 inhibitor developed grade 3/4 neutropenia, as compared with 0.9% of patients who received placebo.
Grade 3/4 leukopenia occurred in 21% of the Ribociclib arm and 0.6% of the placebo group. Hematologic adverse events were uncomplicated and resolved without incident in most cases.
The most common non-hematologic adverse events ( all grades ) were nausea ( 51.5% with Ribociclib vs 28.5% with placebo ), infections ( 50.3% vs 42.4% ), fatigue ( 36.5% vs 30.0% ), and diarrhea ( 35% vs 22.1% ). The events were grade 1/2 severity in most cases.

Rates of discontinuation were 7.5% with Ribociclib and 2.1% with placebo.

Inhibition of CDK 4/6 offers an attractive therapeutic strategy for hormone-receptor breast cancer. CDK 4 and 6, along with their protein regulator, cyclin D1, regulate cell-cycle progression.
CDK4/6 overexpression and amplification of cyclin D1 gene occur frequently in HR-positive breast cancer, and increased CDK 4/6 activity, in particular, is associated with resistance to endocrine therapy. ( Xagena )

Source: Novartis, 2017

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