BYL719 and Letrozole in Post-Menopausal Patients With Hormone Receptor-Positive Metastatic Breast Cancer
Phase: Phase 1
Diagnosis: Breast: Metastatic
NCT ID: NCT01791478
(View complete trial on ClinicalTrials.gov)
DFCI Protocol ID: 13-157
This phase I trial studies the side effects and best dose of the PI3K inhibitor BYL719 when given together with letrozole in treating patients with hormone receptor-positive metastatic breast cancer. The PI3K inhibitor BYL719 may stop the growth of tumor cells by blocking some of the proteins needed for cell growth. Hormone therapy using letrozole may fight breast cancer by blocking the use of estrogen by the tumor cells. Giving the PI3K inhibitor BYL719 together with letrozole may kill more tumor cells
Massachusetts General Hospital, Dana-Farber Cancer Institute, Brigham and Women's Hospital
Ian Krop, MD,
Dana-Farber Cancer Institute
Dejan Juric, MD,
Massachusetts General Hospital
Dana-Farber Cancer Institute:
Breast Cancer Nursing Team, 617-632-3478
Massachusetts General Hospital:
Cancer Trials Call Center, 877-789-6100
- Patients must provide informed written consent.
- Patients must be >/= 18 years of age.
- ECOG performance status 0 - 1.
- Clinical stage IV invasive mammary carcinoma, ER-positive and/or PR-positive by
immunohistochemistry (IHC) and HER2 negative (by IHC or ISH). Patients may have
either measurable or non-measurable disease, both are allowed.
- A minimum of 10 patients in the trial (~50%) will need to have a PIK3CA mutation in
- Patients must have had at least one line of endocrine therapy in the metastatic
setting, or be diagnosed with metastatic breast cancer during or within 1 year of
adjuvant endocrine therapy. There is no limit on lines of prior treatment in the
- Patients must have available tissue (archived formalin-fixed paraffin embedded blocks
(FFPB) or fresh frozen tissue from original diagnosis or metastatic setting) for
correlative studies. Tissue needs to be located and available at the time of
registration (tissue needs to be submitted within 3 weeks of study initiation).
Patients will not be able to start study drugs without tissue availability.
- Life expectancy ≥ 6 months
- Patients must have adequate hematologic, hepatic, and renal function. All laboratory
tests must be obtained less than 1 week from study entry. This includes:
1. ANC >/= 1,500/mm3
2. platelet count >/=100,000/mm3
3. HgB ≥ 9 g/dL
4. Creatinine ≤ 1.5x ULN
5. INR ≤ 2
6. Fasting plasma glucose ≤ 140 mg/dL
7. HgBA1C ≤ 8%
8. Total Serum Bilirubin ≤ 1.5 x ULN (Patients with known Gilbert Syndrome, a total
bilirubin ≤ 3.0 x ULN, with direct bilirubin ≤ 1.5 x ULN)
9. SGOT, SGPT ≤ 3 X ULN if no liver metastasis present
10. SGOT, SGPT ≤ 5 X ULN if liver metastasis present
- Patients must be able to swallow and retain oral medication.
- Patients must be post-menopausal. Post-menopausal female subjects should be defined
prior to protocol enrollment by any of the following:
1. Subjects at least 55 years of age
2. Subjects under 55 years of age and amenorrheic for at least 12 months or
follicle-stimulating hormone (FSH) values ≥ 40 IU/L and estradiol levels </= 20
3. Prior bilateral oophorectomy
4. Prior radiation castration with amenorrhea for at least 6 months
- Patients must complete all screening assessments as outlined in the protocol.
- Locally recurrent resectable breast cancer.
- Any kind of malabsorption syndrome significantly affecting gastrointestinal function.
- Patients with clinically manifest diabetes mellitus (treated and/or clinical signs or
with fasting glucose >/= 140 mg/dL / 7.8 mmol/L), history of gestational diabetes
mellitus or documented steroid-induced diabetes mellitus.
- Patients who have received radiation therapy </= 2 weeks prior to study entry.
Patients who have received prior radiotherapy must have recovered from toxicity (≤
grade 1) induced by this treatment.
- Patients who have received systemic anti-cancer therapy such as chemotherapy,
immunotherapy and/or biologic therapy </= 4 weeks prior to study entry. Concurrent
anti-cancer therapy (chemotherapy, immunotherapy, biologic therapy) other than the
ones specified in the protocol is not permitted during study participation. Patients
must have discontinued the above cancer therapies for 4 weeks prior to the first dose
of study medication, as well as recovered from toxicity (to ≤ than grade 1, except
for alopecia) induced by previous treatments. Any investigational drugs should be
discontinued 4 weeks prior to the first dose of study medication.
- Prior hormonal / endocrine therapy </= 2 weeks prior to study entry. Patients must
have recovered from toxicity > grade 1, except for alopecia.
- Prior therapy with a PI3K inhibitor. Prior use of Akt or mTOR inhibitors are allowed.
- Patients who have received herbal medications </= 2 weeks prior to study entry.
Herbal medications include, but are not limited to: St. John's wort, Kava, ephedra
(ma huang), gingko biloba, dehydroepiandrosterone (DHEA), yohimbe, saw palmetto, and
- Use of drugs that are CYP3A4 modifiers
- Patients who are currently receiving medication with a known risk of prolonging the
QT interval or inducing Torsades de Pointes (TdP) and the treatment cannot either be
discontinued or switched to a different medication prior to starting study drug
- Patients with a family history of congenital long QT syndrome
- Patients with abnormal calcium, potassium, or magnesium levels that cannot be
adequately corrected to within normal range prior to initiation of study drugs
- Uncontrolled intercurrent illness including, but not limited to:
1. ongoing or active infection requiring parenteral antibiotics
2. impairment of lung function (COPD > grade 2, lung conditions requiring oxygen
3. symptomatic congestive heart failure (class III or IV of the New York Heart
Association classification for heart disease)
4. Left Ventricular Ejection Fraction (LVEF) < 50%
5. unstable angina pectoris, angioplasty, stenting, or myocardial infarction within
6. uncontrolled hypertension (systolic blood pressure >140 mm Hg or diastolic blood
pressure > 100 mm Hg, found on two consecutive measurements separated by a 1 or
2-week period despite adequate medical support)
7. clinically significant cardiac arrhythmia (multifocal premature ventricular
contractions, bigeminy,trigeminy, ventricular tachycardia that is symptomatic or
requires treatment [National Cancer Institute -Common Terminology Criteria for
Adverse Events, Version 4.0, grade 3]
8. QTcF ≥ 480 msec on screening EKG
9. known history of QT/QTc prolongation or Torsades de Pointes (TdP)
10. ST depression or elevation of ≥ 1.5 mm in 2 or more leads
11. Diarrhea of any cause ≥ CTCAE grade 2
12. psychiatric illness/social situations that would compromise patient safety or
limit compliance with study requirements including maintenance of a
13. patients with symptomatic brain metastases (patients with a history of brain
metastases must be clinically stable for more than 4 weeks from completion of
14. patients with known history of chronic liver or renal failure
15. patients with known history of chronic or acute pancreatitis
Individuals of all races and ethnic groups are eligible for this trial. There is no bias
towards age or race in the clinical trial outlined. This trial is open to the accrual of