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Tucatinib, Palbociclib and Letrozole in Metastatic Hormone Receptor Positive and HER2-positive Breast Cancer

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ClinicalTrials.gov Identifier: NCT03054363
Recruitment Status : Recruiting
First Posted : February 15, 2017
Last Update Posted : November 7, 2018
Sponsor:
Collaborator:
University of Colorado, Denver
Information provided by (Responsible Party):
University of Colorado, Denver ( Academic Thoracic Oncology Medical Investigators Consortium )

Brief Summary:
This is a multicenter run-in phase Ib / roll-over phase II study of triple targeted drug combination (HER2-targeted small molecule inhibitor tucatinib, CDK4/6 inhibitor palbociclib and aromatase inhibitor letrozole) as a first or second line of therapy in patients with metastatic hormone receptor positive and HER2-positive breast cancer.

Condition or disease Intervention/treatment Phase
Breast Cancer Drug: Tucatinib in Combination with Palbociclib and Letrozole Phase 1 Phase 2

Detailed Description:
This is a multicenter, single arm, open-label, run-in phase Ib / roll-over phase II study of novel HER2-targeted tyrosine kinase inhibitor tucatinib in combination with CDK4/6 inhibitor palbociclib and aromatase inhibitor letrozole in subjects with HR+/HER2+ locally advanced unresectable or metastatic breast cancer. The study will enroll post-menopausal women and premenopausal women if on treatment with or willing to be treated with standard ovarian suppression. The phase Ib part of the study will determine safety and tolerability of the combination of tucatinib, palbociclib and letrozole to confirm that current RP2D of tucatinib and FDA approved dosing of palbociclib remains the same in the triplet combination. The dose of letrozole will be constant through the study period. Once the safety of the combination is established, we will move to the phase II part of the study in the expansion cohort of subjects at RP2D for the purpose of assessing efficacy while further refining assessment of safety of the combination treatment.

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase IB/II Open-label Single Arm Study to Evaluate Safety and Efficacy of Tucatinib in Combination With Palbociclib and Letrozole in Subjects With Hormone Receptor Positive and HER2-positive Metastatic Breast Cancer
Actual Study Start Date : November 13, 2017
Estimated Primary Completion Date : October 2019
Estimated Study Completion Date : October 2020

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Tucatinib in Combination with Palbociclib and Letrozole
During phase 1b part of this trial (N=20 patients), treatment will be administered in cycles of 28 days and consist of tucatinib 300 mg PO BID, palbociclib 125 mg PO daily for 21 days followed by 7 days off, and letrozole 2.5 mg PO daily. Dose modifications of tucatinib, palbociclib and letrozole will be allowed per protocol. There will be an interim safety analysis performed after enrollment of 10 patients. Safety analysis will take into account proportion of patients requiring dose modifications or interruption for therapy because of toxicity. If excessive toxicity or significant changes in PKs are found, further patients will be enrolled at a lower starting dose level. There will be a second interim safety analysis after enrollment of 20 patients in the study. Once the recommended phase II dose (RP2D) has been determined, testing of this drug combination will be expanded in the phase II part of this trial (N=20 patients) to determine the progression-free survival (PFS) rate.
Drug: Tucatinib in Combination with Palbociclib and Letrozole

Starting dose of combination therapy :

Tucatinib 300 mg PO BID Palbociclib 125 mg PO daily 21 day on, 7 days off Letrozole 2.5 mg PO daily

Dose modifications, if necessary:

If Palbociclib toxicity increased:

Tucatinib 300 mg PO BID Palbociclib 100 mg PO daily 21 day on, 7 days off Letrozole 2.5 mg PO daily

If Tucatinib toxicity increased:

Tucatinib 250 mg PO BID Palbociclib 125 mg PO daily 21 day on, 7 days off Letrozole 2.5 mg PO daily

If Palbociclib and Tucatinib toxicity increased:

Tucatinib 250 mg PO BID Palbociclib 100 mg PO daily 21 day on, 7 days off Letrozole 2.5 mg PO daily

Additional dose levels per protocol if PKs indicate a significant change to the metabolism of Tucatinib regardless of clinical toxicity.

Other Names:
  • ONT-380
  • IBRANCE
  • Femara




Primary Outcome Measures :
  1. The number of patients in the Pase 1b part of the study with any adverse events (AE). [ Time Frame: 2.5 years ]
    To measure safety and tolerability of tucatinib used in combination with palbociclib and letrozole (phase Ib part) we will assess the incidence, nature and severity of all adverse events (AE) that occur on or after C1D1 of therapy, AE severities will be classified using the CTCAE criteria.

  2. The number of patients with progression-free survival (PFS) [ Time Frame: 2.5 years ]
    To measure efficacy of tucatinib used in combination with palbociclib and letrozole PFS (phase II part) will be assessed. PFS is defined as the time from allocation to the first documented disease progression according to RECIST 1.1, or death due to any cause, whichever occurs first. For subjects with brain metastatic disease enrolled in the study, assessment of bi-compartmental PFS in the non-CNS and CNS compartments, defined as the time from allocation to the first documented disease progression according to RECIST 1.1 and/or RANO-BM criteria, or death due to any cause, whichever occurs first


Secondary Outcome Measures :
  1. Identify the pharmacokinetic (PK) properties of tucatinib and palbociclib current RP2D. [ Time Frame: 6 months ]
    PK assessments of blood levels of tucatinib and palbociclib will be performed on Cycle 1 Day 15 and Cycle 2 Day 1 of therapy. Plasma samples will be collected to measure levels of tucatinib and its hydroxyl metabolite, as well as levels of palbociclib and its metabolites at steady state on Cycle 1 Day 15. Plasma samples will also be collected prior to administration of tucatinib and palbociclib on the first day of Cycles 2 to assess trough levels.



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Ages Eligible for Study:   18 Years to 100 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Subjects must have a histologically confirmed diagnosis of HR+/HER2+ positive locally advanced unresectable or metastatic breast cancer. Estrogen or progesterone receptor positivity is defined by IHC according to ASCO/CAP guidelines 2010. HER2 positivity is defined by standard of care fluorescence in situ hybridization (FISH) and/or 3+ staining by IHC according to ASCO/CAP guidelines 2014.
  2. Measurable and/or evaluable disease per RECIST 1.1 criteria and/or RANO-BM criteria. Bone only disease is allowed.
  3. CNS inclusion criteria:

    • Subjects without CNS metastases are eligible. Note: brain imaging is not required for asymptomatic subjects without known brain metastatic disease prior to enrollment into the study
    • Subjects with untreated asymptomatic CNS metastases not needing immediate local therapy in the opinion of investigator are eligible. For subjects with untreated asymptomatic CNS lesions > 2.0 cm MRI, discussion with and approval from the Lead PI is required prior to enrollment
    • Subjects with stable brain metastases previously treated with radiation therapy or surgery are allowed to enroll, provided that they are off corticosteroids or on stable/tapering dose of corticosteroids and stability of CNS metastatic disease for at least 4 weeks has been demonstrated, with the last MRI taken within 2 weeks prior to cycle 1 day 1 of the study. Relevant records of any CNS treatment must be available to allow for classification of target and non-target lesions
  4. Age ≥ 18 years
  5. ECOG performance status 0-1
  6. Life expectancy of more than 6 months, in the opinion of the investigator
  7. Study subjects should be post-menopausal women (premenopausal women are eligible if they are on or willing to be on mandatory ovarian function suppression)
  8. Prior treatments:

    • Subjects with newly diagnosed untreated metastatic disease are eligible
    • Subjects who have had 1 line of prior endocrine therapy in the metastatic setting are allowed. Prior adjuvant and/or neoadjuvant endocrine regimens are allowed and not counted towards this limit
    • Subjects may have had up to 1 line of prior chemotherapy, combination of chemotherapy with HER2-targeted antibodies (trastuzumab, pertuzumab, TDM-1), or HER2-targeted therapy alone in the metastatic setting. Prior adjuvant and/or neoadjuvant regimens are allowed and not counted towards this limit
  9. Adequate organ and marrow function as defined below:

    • Absolute neutrophil count ≥ 1,500/mm3
    • Platelets ≥ 75,000/mm3
    • Hemoglobin ≥ 9.0 mg/dL without red blood cell transfusion ≤ 7 days prior to Cycle 1 Day 1 of therapy
    • Total serum bilirubin < 1.5 X upper limit of normal (ULN) except for subjects with known Gilbert's disease, who may enroll if the conjugated bilirubin is ≤ 1.5 ULN
    • AST (SGOT)/ALT (SGPT) ≤2.5 X ULN;
    • Serum creatinine ≤ 1.5 mg/dL
    • International normalized ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5 X ULN unless on medication known to alter INR and aPTT
    • Left ventricular ejection fraction (LVEF) ≥ 50% (as assessed by ECHO or MUGA) documented within 4 weeks prior to first dose of study treatment
    • Serum or urine pregnancy test (for women of childbearing potential) negative ≤ 7 days of starting treatment
  10. Ability to understand and the willingness to sign a written informed consent and comply with the study scheduled visits, treatment plans, laboratory tests and other procedures.
  11. Subject or legally authorized representative of a subject must provide signed informed consent document that has been approved by an institutional review board or independent ethics committee (IRB/IEC) prior to initiation of any study-related tests or procedures that are not part of standard-of-care for the subject's disease.

Exclusion Criteria:

  1. Subjects with previously treated progressing brain metastases are excluded from the study
  2. Subjects with known brain metastases and contraindications to undergo contrast MRI imaging of the brain are excluded from the study
  3. Pregnancy or breast feeding
  4. Current active treatment with an investigational agent.
  5. Known history of hypersensitivity to aromatase-inhibitor drugs.
  6. Any toxicity related to prior cancer therapies that has not resolved to ≤ Grade 1, with the exception of peripheral neuropathy, which must have resolved to ≤ Grade 2, and alopecia.
  7. Previous treatment with lapatinib, neratinib, afatinib, or other investigational EGFR-family receptor tyrosine kinase inhibitor or HER2 tyrosine kinase inhibitor.
  8. Previous treatment with palbociclib, abemaciclib, ribociclib or other investigational CDK4/6 inhibitors
  9. Any systemic anti-cancer therapy (including hormonal therapy), radiation, or experimental agent ≤ 2 weeks of first dose of study treatment
  10. Active bacterial, fungal or viral infections requiring treatment with IV antibiotic, IV anti-fungal, or anti-viral.
  11. Known active hepatitis B (HBV), hepatitis C (HCV) or human immunodeficiency virus (HIV) infections. Note: pretesting is not required.
  12. Inability to swallow pills or any significant gastrointestinal disease which would preclude the adequate oral absorption of medications
  13. Use of prohibited medications listed in Appendix D (strong CYP3A4 or CYP2C8 inducers or inhibitors, or moderate CYP2C8 inhibitor trimethoprim) within 3 elimination half-lives of the inducer or inhibitor prior to first dose of the study treatment
  14. Known myocardial infarction, severe/unstable angina, percutaneous transluminal coronary angioplasty/stenting (PTCA), or coronary artery bypass graft (CABG) within 6 month of the first dose of the study treatment
  15. Clinically significant cardio-vascular disease, such as ventricular arrhythmia requiring therapy, uncontrolled hypertension (defined as persistent systolic blood pressure > 160 mm Hg and/or diastolic blood pressure > 100 mm Hg on antihypertensive medications), or any history of symptomatic CHF
  16. Other severe acute or chronic medical or psychiatric conditions or laboratory abnormalities that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, or in the judgment of the investigator would make the subject inappropriate for entry into the study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03054363


Contacts
Contact: Tiffany Colvin 720-848-0664 tiffany.colvin@ucdenver.edu

Locations
United States, Arizona
University of Arizona Recruiting
Tucson, Arizona, United States, 85724
Contact: Dana Lewallen    520-626-2175    DLewallen@uacc.arizona.edu   
Principal Investigator: Pavani Chalasani         
United States, Colorado
University of Colorado Denver Recruiting
Aurora, Colorado, United States, 80045
Contact: Tiffany Colvin    720-848-0664    tiffany.colvin@ucdenver.edu   
Principal Investigator: Elena Shagisultanova, MD, PhD         
United States, Illinois
Northwestern University Recruiting
Chicago, Illinois, United States, 60611
Contact: Peggy Gilbertsen    312-695-1102    cancertrials@northwestern.edu   
Principal Investigator: William Gradishar         
United States, New Mexico
New Mexico Cancer Care Alliance Recruiting
Albuquerque, New Mexico, United States, 87131
Contact: Karwyn Gustafson    505-925-0380    KSGustafson@salud.unm.edu   
Principal Investigator: Ursa Brown-Glaberman         
United States, New York
Stony Brook University Recruiting
Stony Brook, New York, United States, 11794
Contact: Pushpa Talanki    631-638-0815    Pushpa.talanki@stonybrookmedicine.edu   
Principal Investigator: Alison Stopeck         
United States, Texas
University of Texas Health Science Center San Antonio Recruiting
San Antonio, Texas, United States, 78229
Contact: CTRC    210-450-5798    CTRCReferral@uthscsa.edu   
Principal Investigator: Andrew Brenner         
Sponsors and Collaborators
Academic Thoracic Oncology Medical Investigators Consortium
University of Colorado, Denver
Investigators
Principal Investigator: Elena Shagisultanova, MD, PhD University of Colorado, Denver

Responsible Party: Academic Thoracic Oncology Medical Investigators Consortium
ClinicalTrials.gov Identifier: NCT03054363     History of Changes
Other Study ID Numbers: 16-1661.cc
First Posted: February 15, 2017    Key Record Dates
Last Update Posted: November 7, 2018
Last Verified: November 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No

Keywords provided by University of Colorado, Denver ( Academic Thoracic Oncology Medical Investigators Consortium ):
Metastatic Breast Cancer
Tucatinib
Palbociclib
Letrozole
HR-positive
HER2-positive
ER-positive
PR-positive
HER2-targeted therapy
CDK4/6 inhibitor
ONT-380
Ibrance

Additional relevant MeSH terms:
Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases
Hormones
Letrozole
Palbociclib
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents
Aromatase Inhibitors
Steroid Synthesis Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Estrogen Antagonists
Hormone Antagonists
Protein Kinase Inhibitors