A Randomized Study of TH Versus THL in First Line Treatment of HER2-positive Metastatic Breast Cancer

NCT ID: NCT01526369

Last Updated: 2025-05-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 75 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-02-13
• Study Completion Date: 2023-02-17

Brief Summary

The proposed phase III randomised trial will compare the efficacy of trastuzumab and paclitaxel with trastuzumab, paclitaxel and lapatinib in first line treatment of HER2 positive metastatic breast cancer. The investigators will also examine potential predictive biomarkers of response to trastuzumab and lapatinib in pre-treatment biopsy samples and serum samples.

Conditions

Metastatic Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Paclitaxel and Trastuzumab

Weekly paclitaxel (80mg/m², for 3 weeks of a 4 week cycle) + trastuzumab (8mg/kg loading dose on cycle 1 day 1 and 4mg/kg every 2 weeks) until disease progression, unacceptable toxicity or consent withdrawal.

Group Type: ACTIVE_COMPARATOR

Trastuzumab

Intervention Type: DRUG

Paclitaxel

Intervention Type: DRUG

Paclitaxel, Trastuzumab and Lapatinib

Weekly paclitaxel (80 mg/m², for 3 weeks of a 4 week cycle) + trastuzumab (8 mg/kg loading dose on cycle 1 day 1 and 4 mg/kg every 2 weeks)

+ lapatinib (1,000 mg daily), until disease progression, unacceptable toxicity or consent withdrawal.

Group Type: EXPERIMENTAL

Trastuzumab

Intervention Type: DRUG

Paclitaxel

Intervention Type: DRUG

Lapatinib

Intervention Type: DRUG

Interventions

Trastuzumab

Intervention Type: DRUG

Paclitaxel

Intervention Type: DRUG

Lapatinib

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Written informed consent obtained prior to any study-related procedures

2. Female age 18 years or greater.

3. ECOG Performance Status of 0 or 1.

4. Histologically or cytologically-confirmed invasive metastatic breast cancer.

5. Patients must have measurable disease according to RECIST criteria Version 1.1, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as >20 mm with conventional techniques or as >10 mm with spiral CT scan,MRI, or calipers by clinical exam.

6. Tumour shows HER2 over-expression (3+ by IHC and/or FISH + ) by testing of the primary tumour and if available the biopsied metastatic lesion

7. Patients who received prior radiotherapy must have completed it at least 4 weeks before registration and recovered from all treatment-related toxicities.

8. Cardiac ejection fraction within the institutional range of normal as measured by MUGA or ECHO within 14 days prior to registration. Note that baseline and on treatment scans should be performed using the same modality and preferably at the same institution.

9. Adequate haematological, hepatic, and renal function.

• Haemoglobin ≥ 9g/dL
• Neutrophils (ANC/AGC) ≥1500/mm³ (1.5 x 10^9/L)
• Platelets ≥ (100 x 10^9/L)
• Total bilirubin ≤ 1.5mg/dL (25.65 μmol/L)
• Both ALT (SGPT) and AST (SGOT) ≤ 3 x ULN with or without liver Metastasis
• Alkaline phosphatase ≤ 2.5 x ULN
• Serum creatinine ≤1.5 ULN or calculated creatinine clearance (CrCl) ≥ 30mL/min according to the Cockcroft and Gault formula (Appendix K)

10. Able to swallow and retain oral medication.

11. Women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for the duration of study participation. Female patients of childbearing potential must have pregnancy excluded by urine or serum beta-HCG testing within 7 days prior to registration.

12. Estimated life expectancy greater than 12 weeks

Exclusion Criteria

1. Prior systemic therapy for metastatic disease (except one line of hormonal therapy for metastatic disease without trastuzumab).

2. Recurrence within 12 months from completion of adjuvant chemotherapy to the development of metastatic disease.

3. Recurrence within 6 months from completion of adjuvant trastuzumab to the development of metastatic disease.

4. Prior lapatinib treatment.

5. Peripheral neuropathy ≥ grade 2

6. Patients with known CNS metastasis should be excluded from this clinical trial

7. Prior radiotherapy to more than half of the bony pelvis.

8. Uncontrolled or symptomatic angina, uncontrolled arrhythmias, congestive heart failure, a documented MI within 6 months prior to registration or any other cardiac disorders, which in the opinion of the treating physician, would make this protocol unreasonably hazardous for the patient .

9. Immediate or delayed hypersensitivity or untoward reaction to paclitaxel, trastuzumab, or other related compounds, or to drugs chemically related to lapatinib (including other anilinoquinazolines, e.g. gefitinib (Iressa®) and erlotinib (Tarceva®), or other chemically-related compounds).

10. Pregnant or breastfeeding women are excluded from this study.

11. Patients should not be receiving any other investigational agents (within 30 days prior to registration) or receiving concurrent anticancer therapy.

12. Concomitant requirement for medication classified as CYP3A4 inducers or inhibitors (Table 9).

13. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.

14. Patients with GI tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for IV alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis).

15. Have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment)

16. Concurrent treatment with ovarian hormone replacement therapy. Prior treatment must be stopped prior to registration.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Cancer Trials Ireland

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Helsinki University Hopsital

Helsinki, , Finland

Kuopio University hospital

Kuopio, , Finland

CRLC Val d'Aurelle

Montpellier, , France

Interdisziplinäre Onkologische Zentrum München (IOZ München)

Munich, , Germany

St Vincent's University Hospital

Dublin, Leinster, Ireland

Cork University Hospital

Cork, , Ireland

Beaumont Hospital

Dublin, , Ireland

Mater Misericordiae University Hospital

Dublin, , Ireland

Mater Private Hospital

Dublin, , Ireland

St James's Hospital

Dublin, , Ireland

University Hospital Galway

Galway, , Ireland

Midwestern Regional Hospital

Limerick, , Ireland

Sligo General Hospital

Sligo, , Ireland

Waterford Regional Hospital

Waterford, , Ireland

Rabin Medical Center

Petah Tikva, , Israel

The Chaim Sheba Medical Center

Tel Litwinsky, , Israel

Oslo University Hopsital

Oslo, , Norway

Hospital Santa Maria

Lisbon, , Portugal

Centro Oncologico de Galicia

A Coruña, , Spain

Hospital Nuestra Senora de Sonsoles

Ávila, , Spain

Hospital Infanta Cristina

Badajoz, , Spain

Hospital Virgen de la Luz

Cuenca, , Spain

Hospital General de Grannollers

Granollers, , Spain

Complejo Hospitalario de Jaen

Jaén, , Spain

Hospital Universitari Arnau de Vilanova de Lleida

Lleida, , Spain

Complejo Hospitalario Xeral Calde / Hospital Lucus Augusti

Lugo, , Spain

H. Puerta de Hierro

Madrid, , Spain

Hospital General Universitario Gregorio Maranon

Madrid, , Spain

Hospital de Mataro

Mataró, , Spain

Hospital Infanta Cristina

Parla, , Spain

Hospital Donostia

San Sebastián, , Spain

Hospital Universitario de Canarias

Santa Cruz de Tenerife, , Spain

Hospital General Universitario de Elche

Valencia, , Spain

Hospital General Universitario de Valencia

Valencia, , Spain

Hospital Clinico Universitario 'Lozano Blesa'

Zaragoza, , Spain

Countries

Finland; France; Germany; Ireland; Israel; Norway; Portugal; Spain

Other Identifiers

CTRIAL-IE (ICORG) 11-10

Identifier Type: -

Identifier Source: org_study_id