Contact
Novartis Pharma NV/SA:
+ 32 (0)2 246 16 11
In case of an adverse event:
[email protected]
Phone number 24/h:
Bel: 0800 94 368
Lux: + 32 475 319 792
KISQALI® is reimbursed in Belgium starting July 1st 2025 for use in patients with HR+/HER2- early breast cancer1
For those with HR+/HER2- eBC, this means a 28.5% reduced risk of recurrence at 4 years with KISQALI + NSAI vs NSAI alone.*2
KISQALI is eligible in a broad range of patients with HR+/HER2- eBC, and also offers a manageable safety profile † and maintained QoL.‡1,3 KISQALI can be added as adjuvant treatment up to 12 months following ET initiation.1
Kisqali® is reimbursed in Belgium for use in patients with HR+/HER2- locally advanced or metastatic breast cancer1
* Data from the NATALEE trial (N=5101). Primary endpoint was iDFS. At 3 years, risk of invasive disease was reduced by 25.1% for KISQALI + NSAI vs NSAI alone. HR 0.749; 95% CI: 0.628–0.892. ARR=3.1%.5 At 4 years, risk of invasive disease was reduced by 28.51% for KISQALI + NSAI vs NSAI alone. HR 0.715; 95% CI: 0.609–0.840. ARR=4,9%6.
† The majority of adverse events were transient, manageable, and reversible with dose reduction or interruption.1
‡ The EORTC QLQ-C30 incorporates 5 functional scales (physical, role, cognitive, emotional, and social), 3 symptom scales (fatigue, pain, and nausea and vomiting), a global health status/QoL scale, and a number of single items.4
aBC, advanced breast cancer; AI, aromatase inhibitor; ARR, absolute risk reduction; CI, confidence interval; eBC, early breast cancer; EORTC QLQ-C30, European Organisation for Research and Treatment of Cancer, core quality of life questionnaire; EU, European Union; HER2-, human epidermal growth factor receptor 2 negative; HR, hazard ratio; HR+, hormone receptor positive; LHRH, luteinising hormone releasing hormone; NSAI, nonsteroidal aromatase inhibitor.
References