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Clinical efficacy & safetyPALOMA-2Trial design overviewPatient baseline characteristicsProgression-free survival (primary endpoint)Overall survival (secondary endpoint)Tumour control (secondary endpoint)PALOMA-2 summaryPALOMA-3Trial design overviewPatient baseline characteristicsProgression-free survival (primary endpoint)Overall survival (secondary endpoint)Tumour control (secondary endpoint)SafetySafety overviewPooled laboratory abnormalitiesPALOMA-2 AEsPALOMA-3 AEsSelected safety featuresIBRANCE long-term safetyGI and liver toxicitiesEffect of IBRANCE on QTc intervalElderly patientsVisceral disease patientsDose reduction effect on efficacyRW evidenceValue of RWEWhat is real-world evidence?What is the value of RWE?P-REALITY and P-REALITY XP-REALITY OverviewP-REALITY OS and rwPFSP-REALITY X OverviewP-REALITY X OS and rwPFSIRISIRIS OverviewIRIS PFS and OSPOLARIS POLARIS OverviewPOLARIS Patient-Reported OutcomesMADELINEMADELINE OverviewMADELINE Patient CharacteristicsMADELINE Patient-Reported OutcomesPalomAGEPalomAGE OverviewRWE in Older Patients with mBCPatient-reported outcomesPALOMA-2: FACT-B scoresPALOMA-3: EORTC QLQ-C30 scoresPALOMA-3: Time to deterioration in pain symptomsDosingRecommended dosing scheduleRecommended dose modifications for AEsMonitoringOne scheduled monitoring provision ResourcesMaterials

IBRANCE is indicated for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer:

  • in combination with an aromatase inhibitor;
  • in combination with fulvestrant in women who have received prior endocrine therapy

In pre- or peri-menopausal women, the endocrine therapy should be combined with a luteinising hormone-releasing hormone (LHRH) agonist.1

Please see Full Prescribing lnformation and Patient lnformation

RCT PALOMA 2 & PALOMA 3

PALOMA was the first clinical trial programme to explore how a CDK4/6 inhibitor could benefit women with HR+/HER2- mBC10

Explore PALOMA 2 & PALOMA 3
RWE complements RCTs

With RCT data,1-6 IBRANCE RWE7-9 can help improve understanding of outcomes in patients with HR+/HER2- mBC and help you to better support your patients

Learn more about RWE
Healthcare Professional Resources

Please note the materials are intended for healthcare professionals to effectively support patient care.

Click here for HCP Resources
Provide your patients with proven strength

A broad range of women with HR+/HER2- mBC may benefit from IBRANCE combination therapy.1-9 IBRANCE is the first CDK4/6 inhibitor supported by data from clinical trials1-4 and real-world evidence.5-7

Find out more
TitleAlmost 460,000 patients have been prescribed IBRANCE since FDA approval in 2015, as of January 202211​​​​​​​ Resources Find out more
CDK = cyclin-dependent kinase; FDA = Food and Drug Administration; HR+/HER2- = hormone receptor-positive, human epidermal growth factor 2-negative; mBC = metastatic breast cancer;  RCT = randomised controlled trial; RWE = real-world evidence.References:IBRANCE Summary of Product Characteristics.
Finn RS, et al. N Engl J Med. 2016;375(20):1925-1936.
Rugo H, et al. Breast Cancer Res Treat. 2019;174(3):719-729.
Cristofanilli M, et al. Lancet Oncol. 2016;17(4):425-439.
Cristofanilli M, et al. ASCO 2021; Oral presentation 1000.
Rugo HS, et al. Oncologist. 2021;26(8):e1339-e1346.
DeMichele A, et al. Breast Cancer Res. 2021;23:37.
Taylor-Stokes G, et al. Breast. 2019;43:22-27.
Waller J, et al. J Glob Oncol. 2019;5:JGO1800239.
McCain J. P T. 2015;40(8):511-520.
IBRANCE data on file. Patients prescribed IBRANCE worldwide.

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