Randomized Phase II study of pertuzumab, trastuzumab and vinorelbine in patients with HER2-positive breast cancer.

Conditions: HER2-positive advanced (metastatic or locally advanced) breast cancer
MedDRA version: 14.0Level: LLTClassification code 10065430Term: HER-2 positive breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Therapeutic area: Diseases [C] - Cancer [C04]

Registration Number: EUCTR2011-003308-18-ES

Lead Sponsor: F. Hoffmann-La Roche Ltd.

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Recruiting

Sex: All

Target Recruitment: 210

Inclusion Criteria

1. Signed written informed consent approved by the relevant Institutional Ethical Review Board (IRB).
2. Female or male patients aged 18 years or older.
3. Histologically or cytologically confirmed and documented adenocarcinoma of the breast with metastatic or locally advanced disease not amenable to curative resection.
4. HER2-positive (defined as either immunohistochemistry
[IHC] 3+ or in situ hybridization [ISH] positive) as assessed by local laboratory on primary or metastatic tumor (ISH positivity is defined as a ratio of 2.0 or greater for the number of HER2 gene copies to the number of signals for CEP17, or for single probe tests, a HER2 gene count greater than 4).
5. At least one measurable lesion and/or non-measurable
disease evaluable according to Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1 (Eisenhauer et al. 2009).
6. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
7. Left ventricular ejection fraction (LVEF) of at least 55%.
8. Negative pregnancy test in women of childbearing potential (premenopausal or less than 12 months of amenorrhea post-menopause, and who have not undergone surgical sterilization).
9. For women of childbearing potential who are sexually active, agreement to use a highly effective, nonhormonal form of contraception or two effective forms of non-hormonal contraception during and for at least 6 months post-study treatment.
10. Fertile males willing and able to use effective nonhormonal
means of contraception (barrier method of contraception in conjunction with spermicidal jelly, or surgical sterilization) during and for at least 6 months post-study treatment.
11. Life expectancy of at least 12 weeks.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 100
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 110

Exclusion Criteria

1. Previous systemic non-hormonal anticancer therapy in the
metastatic or locally advanced breast cancer setting.
2. Previous approved or investigative anti-HER2 agents in any breast cancer treatment setting, except trastuzumab and/or
lapatinib in the adjuvant or neoadjuvant setting.
3. Disease progression while receiving trastuzumab and/or
lapatinib in the adjuvant or neoadjuvant setting.
4. Disease-free interval from completion of adjuvant or neo-adjuvant systemic non-hormonal treatment to recurrent disease of less than 6 months.
5. History of persistent Grade 2 or higher (NCI-CTC, Version
4.0) hematological toxicity resulting from previous adjuvant
or neoadjuvant therapy.
6. Radiographic evidence of central nervous system (CNS) metastases as assessed by computed tomography (CT) or
magnetic resonance imaging (MRI).
7. Current peripheral neuropathy of Grade 3 or greater
(NCI-CTC, Version 4.0).
8. History of other malignancy within the last 5 years, except
for carcinoma in situ of the cervix or basal cell carcinoma.
9. Serious uncontrolled concomitant disease that would
contraindicate the use of any of the investigational drugs
used in this study or that would put the patient at high risk for
treatment-related complications.
10. Inadequate organ function, evidenced by the following laboratory results:
? Absolute neutrophil count <1,500 cells/mm3
? Platelet count <100,000 cells/mm3
? Hemoglobin <9 g/dL
? Total bilirubin greater than upper limit of normal (ULN) (unless the patient has documented Gilbert?s syndrome)
? Aspartate aminotransferase AST; SGOT) or alanine aminotransferase (ALT; SGPT) >2.5 × ULN
? AST (SGOT) or ALT (SGPT) >1.5 × ULN with concurrent serum alkaline phosphatase >2.5 × ULN; Serum alkaline phosphatase may be >2.5 × ULN only if bone metastases are present and AST
(SGOT) and ALT (SGPT) <1.5 × ULN
? Serum creatinine >2.0 mg/dL or 177 ?mol/L
? International normalized ratio (INR) and activated partial thromboplastin time (aPTT) or partial thromboplastin time (PTT) >1.5 × ULN (unless on therapeutic coagulation)
11. Uncontrolled hypertension (systolic >150 mm Hg and/or diastolic >100 mm Hg) or clinically significant (i.e. active) cardiovascular disease: cerebrovascular accident (CVA)/stroke or myocardial infarction within 6 months prior to first study medication, unstable angina, congestive heart failure (CHF) of New York Heart Association (NYHA) Grade II or higher, or serious cardiac arrhythmia requiring medication.
12. Current known infection with HIV, HBV, or HCV.
13. Dyspnea at rest due to complications of advanced malignancy, or other disease requiring continuous oxygen therapy.
14. Major surgical procedure or significant traumatic injury within 28 days prior to enrollment into the study or anticipation of need for major surgery during the course of study treatment.
15. Receipt of intravenous (IV) antibiotics for infection within 14 days prior to enrollment into the study.
16. Current chronic daily treatment with corticosteroids (dose
equivalent to or greater than 10 mg/day methylprednisolone),
excluding inhaled steroids.
17. Known hypersensitivity to any of the study medications or to
excipients of recombinant human or humanized antibodies.
18. History of receiving any investigational treatment within 28 days prior to enrollment into the study.
19. Concurrent participation in any clinical trial.
20. Assessed by the investigator to be unable or unwilling to comply with the requirements of the protocol.