Examples of using Combination with trastuzumab in English and their translations into Polish
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TAXOTERE in combination with trastuzumab.
There are currently insufficient data to evaluate the effects of ATA on the efficacy of Perjeta in combination with trastuzumab and docetaxel.
Docetaxel in combination with trastuzumab.
In the pivotal clinical trial CLEOPATRA,408 patients received at least one dose of Perjeta in combination with trastuzumab and docetaxel.
Perjeta in combination with trastuzumab and docetaxel.
Docetaxel Winthrop 100 mg/ m² in combination with trastuzumab.
In combination with trastuzumab the recommended dose of docetaxel is 100 mg/ m2 every three weeks,with trastuzumab administered weekly.
Docetaxel Winthrop in combination with trastuzumab.
Tyverb is prescribed in combination with trastuzumab, for patients who have hormone receptor- negative metastatic breast cancer and have had other treatment for advanced or metastatic breast cancer before.
Docetaxel 100 mg/m² in combination with trastuzumab.
Docetaxel in combination with trastuzumab was studied for the treatment of patients with metastatic breast cancer whose tumours overexpress HER2, and who previously had not received chemotherapy for metastatic disease.
TAXOTERE 100 mg/ m² in combination with trastuzumab.
TAXOTERE in combination with trastuzumab is indicated for the treatment of patients with metastatic breast cancer whose tumors overexpress HER2 and who previously have not received chemotherapy for metastatic disease.
Patients treated with docetaxel in combination with trastuzumab.
When Perjeta was administered in combination with trastuzumab and docetaxel for 3 cycles following 3 cycles of FEC(5-fluorouracil, epirubicin, cyclophosphamide), the most common ADRs(≥50%) were diarrhoea, nausea and alopecia.
Patients treated with docetaxel in combination with trastuzumab.
In combination with trastuzumab for patients with hormone receptor-negative metastatic disease that has progressed on prior trastuzumab therapy(ies) in combination with chemotherapy see section 5.1.
The most common ADRs(≥ 50%) seen with Perjeta in combination with trastuzumab and docetaxel were diarrhoea, alopecia and neutropenia.
Lapatinib retained significant activity against HER2- amplified breast cancer cell lines selected for long-term growth in trastuzumab-containing medium in vitro andwas synergistic in combination with trastuzumab in these cell lines.
The efficacy and safety of lapatinib in combination with trastuzumab in metastatic breast cancer were evaluated in a randomised trial.
Rash occurred in approximately 28% of patients who received lapatinib in combination with capecitabine, in 45% of patients who received lapatinib in combination with letrozole andin 23% of patients who received lapatinib in combination with trastuzumab.
LVEF decreases were reported in 6.7% of patients who received lapatinib in combination with trastuzumab, as compared to 2.1% of patients who received lapatinib alone.
Table 1 summarizes the ADRs from the pivotal trial CLEOPATRA, in which Perjeta was given in combination with docetaxel and trastuzumab to patients with metastatic breast cancer, and from the neoadjuvant trials NEOSPHERE and TRYPHAENA,in which Perjeta was given in combination with trastuzumab and chemotherapy to patients with early breast cancer.
Heart failure has been observed in patients receiving docetaxel in combination with trastuzumab, particularly following anthracycline(doxorubicin or epirubicin)-containing chemotherapy.
The safety of lapatinib has been evaluated as monotherapy or in combination with other chemotherapies for various cancers in more than 20,000 patients, including 198 patients who received lapatinib in combination with capecitabine,149 patients who received lapatinib in combination with trastuzumab and 654 patients who received lapatinib in combination with letrozole see section 5.1.
A multicenter, open-label, single-arm study of pertuzumab in combination with trastuzumab and a taxane in first line treatment of patients with HER2- positive advanced(metastatic or locally recurrent) breast cancer.
In the neoadjuvant trial NEOSPHERE, the most common ADRs(≥50%) seen with Perjeta in combination with trastuzumab and docetaxel were alopecia and neutropenia.
In the neoadjuvant trial TRYPHAENA, when Perjeta was administered in combination with trastuzumab and FEC(5-fluorouracil, epirubicin, cyclophosphamide) for 3 cycles followed by 3 cycles of Perjeta, trastuzumab and docetaxel, the most common ADRs(≥50%) were neutropenia, diarrhoea and nausea.
An increased incidence of LVEF declines was also observed in patients treated with Perjeta in combination with trastuzumab and docetaxel; LVEF recovered to≥50% in all patients.