Table 2.
Medicines | Setting | ESMO-MCBS score | References |
---|---|---|---|
Chemotherapy + trastuzumab | Adjuvant or neoadjuvant HER2-positive tumours | A | 9 |
Trastuzumab and docetaxel + pertuzumab | Neoadjuvant HER2-overexpressed invasive ductal breast | Cb | 10,11 |
Trastuzumab + docetaxel + pertuzumab | First line metastatic | 4 | 12, 13, 14, 15 |
Lapatinib + trastuzumab | Third line metastatic | 4 | 16,17 |
Fulvestrant + palbociclib | Metastatic HR-positive, HER2-negative second line | 4 | 18 |
T-DM1 | Second line metastatic after trastuzumab failure | 4 | 19,20 |
Letrozole + palbociclib | Metastatic HR-positive, HER2-negative first line | 3 | 21 |
Letrozole + palbociclib | Metastatic HR-positive, HER2-negative first line | 3b | 22 |
Letrozole + ribociclib | First line metastatic post-menopause ER/PR positive | 3 | 23 |
Capecitabine + lapatinib | Second line metastatic after trastuzumab failure | 3 | 24 |
Paclitaxel + bevacizumab | First line metastatic, no crossover | 2 | 25 |
Exemestane + everolimus | Metastatic after failure of aromatase inhibitor (with PFS >6 months), no crossover | 2 | 26 |
Eribulin | Third line metastatic after anthracycline and taxane | 2 | 27 |
Eribulin | Third line metastatic after anthracycline and taxane in patients with HER2-negative tumours | 1 | 28 |
Included in the Kazakhstan’s list of medicines (Bolded).
ESMO-MCBS, ESMO-Magnitude of Clinical Benefit Scale; ER, estrogen receptor; HER2, human epidermal growth factor receptor 2; HR, hormone receptor; PFS, progression-free survival; PR, progesterone receptor; T-DM1, trastuzumab emtansine.
Data 2017.
Randomised phase II study.