Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Vejle Hospital
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Woman ≥ 18 years of age.
PS 0-2. Expected lifetime of more than 12 weeks.
Histologically verified breast cancer(adenocarcinoma)
Primary tumor or metastasis is HER2 positive with IHC3+ or FISH+ (ratio ≥ 2.2).
Documented metastatic breast cancer with min. one lesion measureable according to the RECIST 1.1 criteria. All solitary lesions must be verified cytologically/histologically if representing the only evidence of malignancy.
The patient may have received (neo-) adjuvant chemotherapy (taxanes, anthracyclines and trastuzumab) and 1st line chemotherapy in combination with trastuzumab for metastatic disease.
The patient may have received previous adjuvant antihormonal treatment for metastatic breast cancer.
The patient may receive radiation therapy, however, not against lesions used for response evaluation.
Normal heart function, LVEF ≥ 50% measured by MUGA/EKKO.
Normal bone marrow function: Hemoglobin ≥ 6 mmol/l, ANC ≥ 1.5x10\^9/l. Thrombocytes ≥ 100x10\^9/l.
Normal liver function: Bilirubin ≤ 1.5 x upper normal level, ALAT ≤ 2.5 x upper normal level, BASP ≤ 2.5 x upper normal level (≤ 5 if presence of bone metastases).
Normal renal function: Creatinine ≤ upper normal level. In case of raised creatinine the measured/calculated GFR must be ≥ 50 ml/min.
Fertile women must present a negative pregnancy test and use contraceptives during and 3 months after treatment. An IUD without hormone is considered a safe contraceptive.
Written and orally informed consent prior to any study related procedure.
You may not be if
Local recurrence or counter-lateral breast cancer without other dissemination.
Pregnant or breastfeeding women.
Clinical symptoms of CNS metastases, incl. meningeal carcinomatosis.
Malabsorption syndrome or other disease affecting the gastrointestinal function. Resection of the ventriculus or the small intestine, which can affect absorption of oral vinorelbine.
Dysphagia or other conditions preventing the patient from swallowing tablets.
Mental or social conditions preventing treatment or follow-up.
Serious concurrent medical condition, such as:
* AMI within 12 months or unstable angina.
* Heart incompensation NYHA III or IV or uncontrolled hypertension (systolic \> 150 mm/hg and/or diastolic \>100 mm/hg).
