Dr Mark Tuthill patient case study

Indications:1

 

Early breast cancer (eBC)
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 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

Advanced breast cancer (aBC)
KISQALI is indicated for the treatment of women with HR+/HER2– locally advanced or metastatic breast cancer in combination with an AI or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy (ET).

  • In pre/perimenopausal women, the ET should be combined with an LHRH agonist

KISQALI is not recommended to be used in combination with tamoxifen.


Join Dr Mark Tuthill as he shares a case study of his 75-year-old patient who presented with metastatic breast cancer, exploring dose modifications in response to adverse events.

Kisqali Talking Head Case Studies - Dr. Mark Tuthill video VIDEO

Learn more about the safety profile of KISQALI in aBC

Learn more about efficacy in postmenopausal women with HR+/HER2– aBC

aBC,  advanced breast cancer; AI, aromatase inhibitor; eBC, early breast cancer; ET, endocrine therapy; HER2–, human epidermal growth factor receptor 2-negative; HR+, hormone receptor-positive; LHRH, luteinising hormone-releasing hormone; SmPC, summary of product characteristics.

Reference

  1. KISQALI® (ribociclib) Summary of Product Characteristics.

UK | September 2025 | FA-11470852

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.