Phase Ib Trial of LEE011 With Everolimus (RAD001) and Exemestane in the Treatment of Hormone Receptor Positive HER2 Negative Advanced Breast Cancer

Completed · Phase 1

Conditions studied: Breast Cancer

In brief

Dose Escalation part of the study: To estimate the MTD(s) and/ or RP2D of LEE011 in combination with everolimus + exemestane, and LEE011 in combination with exemestane, and to characterize the safety and tolerability of the combinations of everolimus + exemestane + LEE011 and LEE011 + exemestane in patients with ER+ HER2- advanced breast cancer Dose Expansion part of the study: To characterize the safety and tolerability of the triplet combination of LEE011 + everolimus + exemestane in patients naïve or refractory to CDK4/6 inhibitor based therapy, and the safety and tolerability of the doublet combination of LEE011 + exemestane in patients refractory to CDK4/6 inhibitor based therapy (except patients treated with prior LEE011 are not allowed in Group 3).

Key facts

Study ID: NCT01857193
Run by: Novartis Pharmaceuticals
People needed: 132
Starts: 2013-09-06
Expected to finish: 2020-04-16
Last updated by the study team: 2021-04-13

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

Adult women (≥ 18 years of age) with metastatic or locally advanced breast cancer
Histological or cytological confirmation of ER+ breast cancer in dose escalation and HR+ breast cancer in dose expansion
A representative tumor specimen must be available for molecular testing.
Postmenopausal women. Postmenopausal status is defined either by:
Age ≥ 18 with prior bilateral oophorectomy
Age ≥ 60 years
Age <60 years with amenorrhea for at least 12 months and both follicle-stimulating hormone (FSH) and estradiol levels are in postmenopausal range (according to the local laboratory)
Recurrence while on, or within 12 months of end of adjuvant treatment with letrozole or anastrozole, or
Progression while on, or within one month of end of letrozole or anastrozole treatment for locally advanced or metastatic breast cancer.
Patients must have:
Measurable disease*: At least one lesion that can be accurately measured in at least one dimension ≥ 20 mm with conventional imaging techniques or ≥ 10 mm with spiral CT or MRI or
Bone lesions: lytic or mixed (lytic + sclerotic) in the absence of measurable disease as defined above.
ECOG Performance Status 0-1.
Fasting serum cholesterol ≤ 300 mg/dl or 7.75 mmol/L and fasting triglycerides ≤ 2.5 × ULN. In case one or both of these thresholds are exceeded, the patient can only be included after initiation of statin therapy and when the above mentioned values have been achieved
Standard 12-lead ECG values defined as the mean of the triplicate ECGs and assessed by the central laboratory.
QTcF interval at screening < 450 msec (using Fridericia's correction).
Resting heart rate 50-90 bpm

You may not qualify if…

HER2-overexpressing patients by local laboratory testing (IHC 3+ staining or in situ hybridization positive).
Patients who received more than one chemotherapy line for advanced breast cancer.
Previous treatment with exemestane or mTOR inhibitors* (Note:
Patients with disease refractory to prior LEE011 are excluded for dose expansion Group 3 only).
History of brain or other CNS metastases.
Clinically significant, uncontrolled heart disease and/or recent cardiac repolarization abnormality including any of the following:
History of myocardial infarction (MI), angina pectoris, symptomatic pericarditis, or coronary artery bypass graft (CABG) within 6 months prior to study entry
Documented cardiomyopathy
Left ventricular ejection fraction (LVEF) < 50% as determined by Multiple Gated acquisition scan (MUGA) or echocardiogram (ECHO)
Long QT syndrome or family history of idiopathic sudden death or congenital long QT syndrome, and etc.
Clinically significant cardiac arrhythmias, complete left bundle branch block, high-grade AV block
Systolic Blood Pressure (SBP) >160 or <90 mmHg
Patients who are currently receiving treatment with agents that are known to cause QTc prolongation in humans
Patients who are currently receiving treatment (within 7 days prior to starting study treatment) with strong and moderate inhibitors or inducers of CYP3A4/5, substrates of CYP3A4/5 with a narrow therapeutic index or Herbal preparations/medications (Refer to Section 6.4 and Appendix 3)
Inclusion Criteria Exceptions for Phase Ib Dose Expansion patients:
Dose Expansion part of the study has 3 groups, following are the Inclusion Criteria exceptions for these 3 groups
Group 1 - Patients must not have received prior treatment with any CDK4/6 inhibitors
Group 2 - Patients must have disease progression while on or within one month after CDK4/6 inhibitor based therapy
Group 3 - Patients must have disease progression while on or within one month after CDK4/6 inhibitor based therapy (except those patients who received prior LEE011 based therapy).
Other protocol-defined Inclusion/Exclusion may apply.

Where it is running

Highlands Oncology Group — Fayetteville, Arkansas, United States
Sylvester Comprehensive Cancer Center Main Center — Miami, Florida, United States
Massachusetts General Hospital Onc Dept — Boston, Massachusetts, United States
Karmanos Cancer Institute Dept of Onc — Detroit, Michigan, United States
Memorial Sloan Kettering Oncology Dept. — New York, New York, United States
Oregon Health and Science University SC-5 — Portland, Oregon, United States
University of Texas MD Anderson Cancer Center Onc Dept — Houston, Texas, United States
Northwest Medical Specialties — Tacoma, Washington, United States
Novartis Investigative Site — Wilrijk, Belgium
Novartis Investigative Site — Saint-Herblain, France
Novartis Investigative Site — Hong Kong, Hong Kong
Novartis Investigative Site — Barcelona, Catalonia, Spain
Novartis Investigative Site — L'Hospitalet de Llobregat, Catalonia, Spain

Full record on ClinicalTrials.gov

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