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Dr John Crown explains the reasoning behind the 3-years duration of treatment for KISQALI® (ribociclib)
Indications:1
KISQALI, in combination with an aromatase inhibitor (AI), is indicated for the adjuvant treatment of patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative early breast cancer (eBC) at high risk of recurrence (see section 5.1 of the SmPC for selection criteria).
In pre/perimenopausal women, or in men, the AI should be combined with a luteinising hormone-releasing hormone (LHRH) agonist
KISQALI is not recommended to be used in combination with tamoxifen.
For information on the safety profile of KISQALI in eBC, click here.
Please consult your local Summary of Product Characteristics for the full KISQALI safety and tolerability profile.
Click the play button below to watch the video from Dr John Crown
Watch Dr John Crown discuss the reasons why a three-year treatment duration was chosen for the NATALEE trial.
AI, aromatase inhibitor; eBC, early breast cancer; HER2–, human epidermal growth factor receptor 2-negative; HR+, hormone receptor-positive; LHRH, luteinising hormone-releasing hormone; SmPC, summary of product characteristics.
Reference
KISQALI® (ribociclib) Summary of Product Characteristics.
UK | November 2025 | FA-11547253
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.