ALTTO (Adjuvant Lapatinib and/or Trastuzumab Treatment Optimisation) study
- Conditions
- Operable primary breast cancer with over expression/ amplification of HER2.MedDRA version: 20.0Level: PTClassification code 10006187Term: Breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)Therapeutic area: Diseases [C] - Cancer [C04]
- Registration Number
- EUCTR2006-000562-36-AT
- Lead Sponsor
- ovartis Pharma Services AG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 8000
1. Age > or = 18 years;
2. Eastern Cooperative Oncology Group performance status < or = 1;
3. Non-metastatic operable primary invasive adenocarcinoma of the breast fulfilling the following:
a. Histologically confirmed;
b. Adequately excised (exceptions: patients who have 'non-resectable' deep margin invasion or histologically documented infiltration of the skin (pT4) are eligible provided they have had or will receive radiotherapy);
c. Axilla dissected; sentinel node sampling is allowed provided that axillary dissection follows confirmation of a positive sentinel node (sentinel node sampling alone is not acceptable after neo-adjuvant chemotherapy);
d. Axillary node positive patient or node negative patient with a tumor of more than 1 cm in greatest diameter (> or = T1c);
4. Known hormone receptor status (ER/PgR or ER alone);
5. Must have received at least four cycles of an approved anthracycline-based (neo-) adjuvant chemotherapy regimen;
For design 1: Randomisation must be performed no longer than 12 weeks from day 1 of the last chemotherapy cycle.
For design 2: Randomisation must be performed no longer than 6 weeks from day 1 of the last anthracycline-containing chemotherapy cycle.
For design 1 & 2: Study treatment should start no more than 14 days after randomisation;
6. Baseline LVEF > or = 50% after completion of all anthracycline-based (neo-) adjuvant chemotherapy and prior to the targeted therapy(ies);
7. Confirmed overexpression and/or gene amplification of ErbB2 (HER2) in the invasive component of the primary tumour, according to one of the following definitions:
– 3+ overexpression by IHC (>30% of invasive tumour cells);
– 2+ or 3+ (in 30% or less neoplastic cells) overexpression by IHC and positive in situ hybridisation (FISH/CISH) test;
– ErbB2 (HER2) gene amplification by FISH/CISH;
- Patients with a negative or equivocal overall result for overexpression and/or gene amplification are not eligible for participation in the trial;
- Equivocal local results may be submitted for a final determination by the central laboratory.
8. Completion of all necessary baseline laboratory and radiological investigations;
9. Signed written informed consent prior to any study specific screening procedures.
Are the trial subjects under 18? no
Number of subjects for this age range: 0
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 4000
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 4000
Patients meeting any of the following criteria are not eligible for this study:
1. History of any prior (ipsi- and/or contralateral) invasive breast carcinoma;
2. Past (less than 10 years) or current history of malignant neoplasms, unless curatively treated basal and squamous cell carcinoma of the skin or carcinoma in situ of the cervix;
NOTE: Patients with a prior malignancy diagnosed greater than 10 years in the past who have been curatively treated with surgery ONLY, WITHOUT radiation therapy or systemic therapy (chemotherapy or
endocrine) are eligible for the study. Patients with any prior diagnosis of breast cancer or melanoma, at any time, are excluded from this study.
3. Any clinically staged T4 tumour, including inflammatory breast cancer;
4. Bilateral tumours;
5. Maximum cumulative dose of doxorubicin >360mg/m2 or maximum cumulative dose of epirubicin >720mg/m2 or any prior anthracyclines unrelated to the present breast cancer;
6. Previous (neo-) adjuvant chemotherapy with peripheral stem cell or bone marrow stem cell support;
7. Any prior mediastinal irradiation except internal mammary node irradiation for the present breast cancer;
8. Patients with positive or suspicious internal mammary nodes identified by sentinel node technique which have not been irradiated or will not be irradiated, or patients with supraclavicular lymph node involvement;
9. Prior anti-ErbB2 (HER2) therapy for any reason, or other prior biologic or immunotherapy for breast cancer;
10. Concurrent anti-cancer treatment, except hormonal therapy or radiotherapy for the present breast cancer;
11. Concurrent anti-cancer treatment in another investigational trial with hormone therapy or immunotherapy unless approved by the Executive Committee;
12. Serious cardiac illness or medical conditions including but not confined to:
– History of documented congestive heart failure (CHF) or systolic dysfunction (LVEF < 50%) ;
– High-risk uncontrolled arrhythmias (ventricular tachycardia, high-grade AV-block, supraventricular arrhythmias which are not adequately rate-controlled);
– Angina pectoris requiring antianginal medication;
– Clinically significant valvular heart disease;
– Evidence of transmural infarction on ECG;
– Poorly controlled hypertension (e.g. systolic >180mm Hg or diastolic >100mm Hg);
13. Other concurrent serious diseases that may interfere with planned treatment including severe pulmonary conditions/illness;
14. Any of the following abnormal laboratory tests immediately prior to randomisation:
– serum total bilirubin;
– alanine amino transferase (ALAT) or aspartate amino transferase (ASAT);
– alkaline phosphatase (ALP);
– serum creatinine;
– total white blood cell count (WBC);
– absolute neutrophil count;
– platelets;
15. Unresolved or unstable serious toxicity from prior adjuvant chemotherapy or radiotherapy;
16. Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel, or persons unable to swallow oral medication. Patients with ulcerative colitis are also excluded;
17. Pregnant, lactating (women of childbearing potential must have a negative pregnancy test - urine or serum - within 7 days prior to randomisation);
18. Women of childbearing potential including women whose last menstrual period was <1 year ago (unless surgically sterile) who are unable or unwilling to use adequate contraceptive measures during study
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method