Clinical Trials /

Lapatinib Plus Chemotherapy Versus Trastuzumab Plus Chemotherapy in HER2-positive Breast Cancer

NCT03273595

Description:

This is a prospective, open-label, real-word study evaluating the efficacy and safety of lapatinib in combination with chemotherapy versus trastuzumab in combination with chemotherapy in women with HER2-positive and p95HER2-positive ,or PI3K mutation, or PTEN loss breast cancer . Eligible subjects will have newly diagnosed breast cancer (Stage II-III) ; not have received systemic or local treatment . The primary endpoint was the rate of pathological complete response (pCR). The secondary objectives are to evaluate overall survival, overall response rate, clinical benefit response rate and the safety as well as tolerability of lapatinib plus chemotherapy and trastuzumab plus chemotherapy. Patients will receive lapatinib 1000 mg daily or trastuzumab 4 mg/kg intravenous (IV) load followed by 2 mg/kg IV weekly for a total of 12 weeks. After surgery, patients planned total duration of the anti-HER2 therapy will be one year.

Related Conditions:
  • Breast Carcinoma
Recruiting Status:

Recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: Lapatinib Plus Chemotherapy Versus Trastuzumab Plus Chemotherapy in HER2-positive Breast Cancer
  • Official Title: A Prospective, Open-label,Multicentre,Real-word Study of Lapatinib Plus Chemotherapy Versus Trastuzumab Plus Chemotherapy as Neoadjuvant Therapy for Women With HER2-positive and p95HER2-positive,PI3K Mutation,or PTEN Loss Breast Cancer

Clinical Trial IDs

  • ORG STUDY ID: KY20162048-1
  • NCT ID: NCT03273595

Conditions

  • Neoplasms, Breast

Interventions

DrugSynonymsArms
LapatinibExperimental group
TrastuzumabControl
PaclitaxelControl
EpirubicinControl
CyclophosphamideControl

Purpose

This is a prospective, open-label, real-word study evaluating the efficacy and safety of lapatinib in combination with chemotherapy versus trastuzumab in combination with chemotherapy in women with HER2-positive and p95HER2-positive ,or PI3K mutation, or PTEN loss breast cancer . Eligible subjects will have newly diagnosed breast cancer (Stage II-III) ; not have received systemic or local treatment . The primary endpoint was the rate of pathological complete response (pCR). The secondary objectives are to evaluate overall survival, overall response rate, clinical benefit response rate and the safety as well as tolerability of lapatinib plus chemotherapy and trastuzumab plus chemotherapy. Patients will receive lapatinib 1000 mg daily or trastuzumab 4 mg/kg intravenous (IV) load followed by 2 mg/kg IV weekly for a total of 12 weeks. After surgery, patients planned total duration of the anti-HER2 therapy will be one year.

Trial Arms

NameTypeDescriptionInterventions
ControlPlacebo Comparator
  • Trastuzumab
  • Paclitaxel
  • Epirubicin
  • Cyclophosphamide
Experimental groupExperimental
  • Lapatinib
  • Paclitaxel
  • Epirubicin
  • Cyclophosphamide

Eligibility Criteria

        Inclusion Criteria:

          -  Female gender;

          -  Age ≥18 years;

          -  Performance Status- Eastern Cooperative Oncology Group (ECOG) 0-1

          -  Histologically confirmed invasive breast cancer:

          -  Primary tumour greater than 2 cm diameter, measured by clinical examination and
             mammography or echography,

          -  p95HER2 positive,or PI3K mutation,or PTEN loss

          -  Over expression and/or amplification of HER2 in the invasive component of the primary
             tumour [Wolff et al 2006] and confirmed by a certified laboratory prior to
             randomisation

          -  Known hormone receptor status.

          -  Haematopoietic status:

          -  Cardiovascular:

          -  Baseline left ventricular ejection fraction (LVEF) ³ 50% measured by echocardiography
             (ECHO) or Multiple Gate Acquisition (MUGA) scan,

          -  Negative serum pregnancy test, within 2-weeks (preferably 7 days) prior to
             randomization (For women of childbearing potential)

          -  Fertile patients must use effective contraception (barrier method - condoms, diaphragm
             - also in conjunction with spermicidal jelly, or total abstinence. Oral, injectable,
             or implant hormonal contraceptives are not allowed)

          -  Signed informed consent form (ICF)

          -  Patient accepts to make available tumour samples for submission to central laboratory
             to conduct translational studies as part of this protocol

        Exclusion Criteria:

          -  Received any prior treatment for primary invasive breast cancer;

          -  Previous (less than 10 years) or current history of malignant neoplasms, except for
             curatively treated:

          -  Basal and squamous cell carcinoma of the skin;

          -  Carcinoma in situ of the cervix.

          -  Patients with a prior malignancy diagnosed more than 10 years prior to randomisation
             may enter the study. Patients must have been curatively treated with surgery alone.
             Radiation therapy or systemic therapy (chemotherapy or endocrine) are NOT permitted.
             Prior diagnoses of breast cancer or melanoma are excluded.

          -  Diagnosis of inflammatory breast cancer;

          -  Bilateral cancer;

          -  This criterion has been deleted from the protocol Version 1. Patients with multi-focal
             cancer are no longer excluded.

          -  Known history of uncontrolled or symptomatic angina, clinically significant
             arrhythmias, congestive heart failure, transmural myocardial infarction, uncontrolled
             hypertension (≥180/110), unstable diabetes mellitus, dyspnoea at rest, or chronic
             therapy with oxygen;

          -  Concurrent disease or condition that would make the subject inappropriate for study
             participation or any serious medical disorder that would interfere with the subject's
             safety;

          -  Unresolved or unstable, serious adverse events from prior administration of another
             investigational drug;

          -  Active or uncontrolled infection;

          -  Dementia, altered mental status, or any psychiatric condition that would prevent the
             understanding or rendering of ICF;

          -  Malabsorption syndrome, disease significantly affecting gastrointestinal function, or
             resection of the stomach or small bowel. Subjects with ulcerative colitis are also
             excluded;

          -  Concurrent neoadjuvant cancer therapy (chemotherapy, radiation therapy, immunotherapy,
             biologic therapy other than the trial therapies);

          -  Concurrent treatment with an investigational agent or participation in another
             therapeutic clinical trial;

          -  Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs
             chemically related to trastuzumab or lapatinib or their excipients;

          -  Pregnant or lactating women;

          -  Concomitant use of CYP3A4 inhibitors or inducers
      
Maximum Eligible Age:70 Years
Minimum Eligible Age:18 Years
Eligible Gender:Female
Healthy Volunteers:No

Primary Outcome Measures

Measure:pathological complete response (pCR)
Time Frame:at the end of week 12
Safety Issue:
Description:

Details

Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Xijing Hospital

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