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Breast CancerPhase 1NCT03846583

Tucatinib + Abemaciclib + Herceptin for HER2+ MBC

A Phase 1 study testing Tucatinib, Abemaciclib and Trastuzumab in people with Breast Cancer, run by Dana-Farber Cancer Institute.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This research study is studying a combination of drugs as a possible treatment for HER2-Postive Metastatic Breast Cancer. The interventions involved in this study are: Tucatinib Abemaciclib (VerzenioTM) Trastuzumab (Herceptin®) Endocrine Therapy: Exemestane (Aromasin®), Letrozole (Femara®), or Anastrozole (Arimidex®) Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Breast Cancer
What is being tested?
Tucatinib, Abemaciclib and Trastuzumab
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
No sites listed yet
Study dates
28 Jun 2020to 22 Sep 2020
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Dose Escalation Cohort:
  • At least one measurable or non-measurable metastasis by radiographic evaluation or physical examination.
  • Progressive breast cancer on most recent regimen
  • Presence of CNS metastases allowed, but not required for participation in the dose escalation cohort.
  • Expansion Cohort A:
  • At least one measurable CNS metastasis per RANO-BM, defined as ≥ 10 mm in at least one dimension.
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  • Unequivocal evidence of new and/or progressive brain metastases, and at least one of the following scenarios:
  • Treated with SRS or surgery with residual un-treated lesions remaining. Such participants are eligible for immediate enrollment on this study providing that at least one untreated lesion is measurable
  • Participants who have had prior WBRT and/or SRS and then whose lesions have subsequently progressed are also eligible. In this case, lesions which have been treated with SRS may be considered as target lesions if there is unequivocal evidence, in the opinion of the treating physician, of progression following SRS.
  • Participants who have not previously been treated with cranial radiation (e.g., WBRT or SRS) are eligible to enter the study, but such participants must be asymptomatic from their CNS metastases and not requiring corticosteroids for symptom control.
  • Both participants who present with systemic stable/absent or systemic progressive disease are eligible, as long as they fulfill one of the above criteria.
  • Expansion Cohort B:
  • New and/or progressive brain metastasis(es) with clinical indication for surgical resection.
  • Participants must have evaluable intracranial disease according to RANO-BM prior to surgical resection. Should participants also have extracranial disease, it may be evaluable according to RECIST 1.1
  • Expansion Cohort C:
  • -At least one measurable extracranial metastasis according to RECIST 1.1
  • All Cohorts:
  • Pathologically confirmed Hormone Receptor (HR)-positive HER2-positive MBC by local laboratory with the following requirements:
  • To fulfill the requirement of HR-positive disease, the most recent biopsy (primary tumor or metastatic lesion) of the breast cancer must express at least one of the hormone receptors (estrogen receptor [ER] or progesterone receptor [PR]) by immunohistochemistry (IHC). ER and PR assays are considered positive if there are > 1% positive tumor nuclei in the sample.
  • To fulfill the requirement of HER2-positive disease, the most recent biopsy (primary tumor or metastatic lesion) of the breast cancer must demonstrate HER2 overexpression or amplification (immunohistochemistry of 3+ or HER2 gene amplification by in situ hybridization with a ratio of HER2-gene signals to centromere 17 signals ≥ 2.0 or average HER2 copy number ≥ 6.0 signals/cells).
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
  • Left ventricular ejection fraction (LVEF) ≥ 50% by echocardiogram (echo) or multigated acquisition (MUGA) scan within 3 months before initiation of study treatment. Patients with a history of LVEF < 50% should have left ventricular ejection fraction (LVEF) ≥ 50% by echocardiogram (echo) or multigated acquisition (MUGA) scan within the screening window.
  • Stable or decreasing corticosteroid dose for at least 7 days prior to initiation of treatment.
  • Concurrent administration of other anti-cancer therapy during the course of this study is not allowed, except for hormonal therapy with one of the commercially available aromatase inhibitors (AI) and the use of ovarian suppression in pre-menopausal patients. Note that concurrent use of supportive care medications (e.g. anti-resorptive agents, pain medications) is allowed. Pre-menopausal patients will need to receive ovarian suppression with the use of one of the commercially available GNRH agonists, per the choice of the treating physician.
  • The subject is ≥18 years old.
  • Participants must have normal organ and marrow function as defined below:
  • Absolute neutrophil count ≥ 1.5 × 109/L
  • Platelets ≥ 100 × 109/L
  • Hemoglobin ≥ 8 g/dL
  • Note: Patients may receive erythrocyte transfusions to achieve this hemoglobin level at the discretion of the investigator. Initial treatment must not begin earlier than the day after the erythrocyte transfusion.
  • Total bilirubin ≤ 1.5 × ULN.
  • Patients with Gilbert's syndrome with a total bilirubin ≤ 2.0 times ULN and direct bilirubin within normal limits are permitted;
  • AST(SGOT)/ALT(SGPT) ≤ 3.0 × institutional ULN.
  • Albumin > 2.5mg/dL
  • Serum creatinine ≤ 1.5 × ULN.
  • Female subjects of childbearing potential must have a negative serum or urine pregnancy test prior to initiating protocol therapy.
  • The effects of tucatinib, abemaciclib, and trastuzumab on the developing human fetus are unknown so women of child-bearing potential and men must agree to use adequate contraception (barrier method of birth control; abstinence) prior to study entry and for the duration of study participation and 4 months after completion of tucatinib and abemaciclib administration and 7 months after trastuzumab administration.
  • The subject is capable of understanding and complying with the protocol and has signed the informed consent document.
  • Participant must be able to swallow and retain oral medication.
  • Have discontinued all previous therapies for breast cancer (including chemotherapy, radiotherapy, immunotherapy, and investigational therapy), except for trastuzumab, for at least the following number of days prior to receiving study drug(s):
  • 28 days for myelosuppressive agents given every 28-day schedule.
  • 21 days for myelosuppressive agents given every 21-day schedule.
  • 14 days for myelosuppressive agents given every 7-day schedule, or for oral agents or for nonmyelosuppresive agents
  • Patients must have recovered from the acute effects of therapy (until the toxicity resolves to either baseline or at least Grade 1) except for residual alopecia or peripheral neuropathy

Who cannot join

  • Visceral crisis or impending visceral crisis at time of screening.
  • CNS complications for whom urgent neurosurgical intervention is indicated (e.g., resection, shunt placement).
  • Known leptomeningeal metastases [Defined as positive CSF cytology and/or unequivocal radiological evidence of clinically significant leptomeningeal involvement. CSF sampling is not required in the absence of suggestive symptoms to exclude leptomeningeal involvement].
  • Patients unable to undergo gadolinium contrast-enhanced MRI or receive IV gadolinium contrast for any reason (e.g., due to pacemaker, ferromagnetic implants, claustrophobia, extreme obesity, hypersensivity).
  • Has received prior therapy with a CDK4/6 inhibitor.
  • No washout is required for endocrine therapy. If a patient has been on ovarian suppression for at least 28 days prior to study entry, ccontinuation of ovarian suppression is permitted on protocol. Patients can receive a new form of endocrine therapy with one of the commercially available AIs at the time of initiation of protocol therapy.
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  • Subjects with a history of grade 3 or 4 allergic reactions attributed to compounds of similar biologic composition to tucatinib and/or abemaciclib or any constituent of the product(s).
  • The subject has an uncontrolled intercurrent illness, including, but not limited to, ongoing or active infection, uncontrolled hypertension, unstable angina pectoris, uncontrolled cardiac arrhythmia, congestive heart failure-New York Heart Association Class III or IV, active ischemic heart disease, myocardial infarction within the previous six months, uncontrolled diabetes mellitus, gastric or duodenal ulceration diagnosed within the previous 6 months, chronic liver or renal disease, or severe malnutrition.
  • The subject is pregnant or breast-feeding.1No active, second potentially life-threatening cancer. Exceptions include non-melanoma skin cancers, curatively treated in situ cancer of the cervix, DCIS, stage1/grade 1 endometrial carcinoma.
  • Has had major surgery within 21 days before treatment initiation.
  • Active infection requiring iv antibiotics at the time of treatment initiation.
  • Symptomatic intrinsic lung disease or extensive tumor involvement of the lungs, resulting in dyspnea at rest.
  • Known intolerance to trastuzumab.
  • Patients may not be receiving concurrent therapy with strong inhibitors of CYP3A4 or strong inhibitors or inducers of CYP2C8. Please refer to Appendix M for a list of inhibitors and inducers. Please note that concurrent use of trimethoprim, a component of Bactrim, is prohibited per protocol. Patients who require PCP prophylaxis will need to switch to an alternative antibiotic (e.g. mepron)

About this study

Official title: Phase Ib Trial of Tucatinib in Combination With Abemaciclib and Trastuzumab for Patients With HER2-Positive Metastatic Breast Cancer

This research study is studying a combination of drugs as a possible treatment for HER2-Postive Metastatic Breast Cancer.

The interventions involved in this study are:

  • Tucatinib
  • Abemaciclib (VerzenioTM)
  • Trastuzumab (Herceptin®)
  • Endocrine Therapy: Exemestane (Aromasin®), Letrozole (Femara®), or Anastrozole (Arimidex®)
Read the detailed description

This research study is a Phase Ib clinical trial, which tests the safety of an investigational intervention and also tries to define the appropriate dose of the investigational intervention to use for further studies. "Investigational" means that the intervention is being studied. The U.S. Food and Drug Administration (FDA) has not approved the combination of Tucatinib, Abemaciclib, and Trastuzumab as a treatment for any disease.

In this research study, the investigators are:

  • Studying the combination of Tucatinib, Abemaciclib, Trastuzumab, and hormonal therapy.
  • Tucatinib is a drug that inhibits human epidermal growth factor receptor 2 (HER-2) protein, which is a protein expressed in the cancer cells. By inhibiting this protein, tucatinib may help stop or reduce the growth of the tumor. The U.S. Food and Drug Administration (FDA) has not approved Tucatinib as a treatment for any disease, but it has been used in a research setting with humans for many years.
  • Abemaciclib is a cyclin-dependent kinase (CDK) inhibitor. CDK inhibitors work to stop cell growth. The FDA has not approved Abemaciclib for this specific disease, but it has been approved for other uses.
  • Trastuzumab is called a "targeted therapy" because it works by attaching itself to specific receptors on the surface of breast cancer cells, known as HER2 receptors. When Trastuzumab attaches to HER2 receptors, the signals that tell the cells to grow are blocked and the cancer cell may be marked for destruction by your immune system. This process allows trastuzumab to help slow or stop the growth of the breast cancer. The FDA has approved Trastuzumab as a treatment for this disease.
  • Exemestane, Letrozole, and Anastrozole belong to a class of drugs called aromatase inhibitors. the participant and the physician will choose the most appropriate aromatase inhibitor for them. These drugs act by lowering the amount of estrogen produced by the body by blocking an enzyme called aromatase. Each of these drugs have been approved by the FDA for this cancer and have been used in the treatment of metastatic ER-positive breast cancer for many years.
  • In this part of the research study the investigators are looking for the safest doses of these drugs to give to participants at the same time.
  • The overall goal of this study is to evaluate the safety and effectiveness of Tucatinib in combination with Abemaciclib, Trastuzumab, and hormonal therapy for hormone receptor-positive, HER2-positive Metastatic Breast Cancer
Conditions
Breast Cancer
Being tested
Tucatinib, Abemaciclib, Trastuzumab, Aromatase Inhibitor
Keywords
Breast Cancer
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TucatinibDrug

    Tucatinib is a drug that inhibits human epidermal growth factor receptor 2 (HER-2) protein, which is a protein expressed in the cancer cells. By inhibiting this protein, tucatinib may help stop or reduce the growth of the tumor

  • AbemaciclibDrug

    Also called Verzenio

    Abemaciclib is a cyclin-dependent kinase (CDK) inhibitor. CDK inhibitors work to stop cell growth.

  • TrastuzumabDrug

    Also called Herceptin

    • Trastuzumab is called a "targeted therapy" because it works by attaching itself to specific receptors on the surface of breast cancer cells, known as HER2 receptors. When Trastuzumab attaches to HER2 receptors, the signals that tell the cells to grow are blocked and the cancer cell may be marked for destruction by the immune system.

  • Aromatase InhibitorDrug

    These drugs act by lowering the amount of estrogen produced by the body by blocking an enzyme called aromatase

Study groups in NCT03846583
Study groupRoleWhat they receive
Dose EscalationExperimental* Tucatinib is administered orally twice daily * Abemaciclib is administered orally twice daily * Trastuzumab is adminidtered intravenously once every three weeks * Aromatase Inhibitor is administered orally once daily
Receives: Drug: Tucatinib; Drug: Abemaciclib; Drug: Trastuzumab; Drug: Aromatase Inhibitor
Arm A: Active Brain MetastasesExperimental* Tucatinib is administered orally twice daily * Abemaciclib is administered orally twice daily * Trastuzumab is adminidtered intravenously once every three weeks * Aromatase Inhibitor is administered orally once daily
Receives: Drug: Tucatinib; Drug: Abemaciclib; Drug: Trastuzumab; Drug: Aromatase Inhibitor
Arm B: Surgical Resection NeededExperimental* Tucatinib is administered orally twice daily * Abemaciclib is administered orally twice daily * Trastuzumab is adminidtered intravenously once every three weeks * Aromatase Inhibitor is administered orally once daily
Receives: Drug: Tucatinib; Drug: Abemaciclib; Drug: Trastuzumab; Drug: Aromatase Inhibitor
Arm C: Progressive Extracranial DiseaseExperimental* Tucatinib is administered orally twice daily * Abemaciclib is administered orally twice daily * Trastuzumab is adminidtered intravenously once every three weeks * Aromatase Inhibitor is administered orally once daily
Receives: Drug: Tucatinib; Drug: Abemaciclib; Drug: Trastuzumab; Drug: Aromatase Inhibitor

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The Maximum Tolerated Dose

    Determine recommended MTD for phase 2 combination of tucatinib with abemaciclib and trastuzumab.

    Measured: 2 years

Secondary outcomes (9)

  1. Overall Response Rate

    Efficacy of study combination, defined by CNS ORR according to RANO-BM.

    Measured: 20 year

  2. Duration of Response

    DOR in the CNS according to RANO-BM.

    Measured: 2 years

  3. Extracranial ORR

    Extracranial ORR according to RECIST 1.1.

    Measured: 2 Years

  4. Progression Free Survival

    Bi-compartmental progression-free survival (PFS) according to RANO-BM.

    Measured: 2 years

  5. Duration of Extracranial Response

    Duration of Extracranial Response according to RANO-BM.

    Measured: 2 Years

  6. Overall Survival

    OS will be analyzed using Kaplan-Meier product-limit estimates and 90% confidence bands

    Measured: 2 Years

  7. Site of First Progression

    Site of First Progression, CNS vs extracranial vs both

    Measured: 2 Year

  8. Extra-CNS response rates

    Extra-CNS response rates according to RECIST 1.1

    Measured: 2 years

  9. Number of participants with treatment-related adverse events as assessed by CTCAE v5.0

    to evaluate the number of participants with treatment-related adverse events as assessed by CTCAE v5.0

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Feb 2019
  2. Study start28 Jun 2020 (estimated)
  3. Primary completion22 Sep 2020
  4. Study completion22 Sep 2020

Why it stopped: Study halted prematurely, prior to enrollment of first participant.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Sequential
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03846583
Sponsor's protocol ID
18-621
Status last verified
Oct 2020
First submitted
13 Feb 2019
Last updated
23 Oct 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: The Dana-Farber / Harvard Cancer Center encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: \[contact information for Sponsor Investigator or designee\]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Tucatinib, Abemaciclib and Trastuzumab in people with Breast Cancer, run by Dana-Farber Cancer Institute.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 44 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 23 Oct 2020. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The Maximum Tolerated Dose (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03846583.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Oct 2020; AzTrials last refreshed its copy on 31 Oct 2026.

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