Review Article
Combination Drug Delivery Approaches in Metastatic Breast Cancer
Table 1
Clinically used combination regimens of nonspecific small molecule chemotherapeutic agents in metastatic breast cancer.
| Classes | Regimens | Advantages | Disadvantages | References |
| | Doxorubicin + Cyclophosphamide | | | | Anthracycline based | Doxorubicin + Fluorouracil | Improved RR | No significant difference in time to progression or survival, more treatment related toxicity, and less quality of life | [23, 24] | | Epirubicin + Cyclophosphamide | | | | | Epirubicin + Fluorouracil | | | |
| | Doxorubicin + Paclitaxel | Improved RR and PFS | More hematologic toxicity, cardiotoxicity | [18, 28] | Taxane based | Doxorubicin + Docetaxel | | | | Capecitabine + Docetaxel | Improved TTP, RR, and OS | Increased nonhematologic toxicity (diarrhea, stomatitis, hand-foot syndrome) | [25, 29, 30] | | Gemcitabine + Paclitaxel | | | |
| Other combinations | Ixabepilone + Capecitabine | Improved RR and TTP in heavily pretreated patient | Peripheral neuropathy | [27] | Cyclophosphamide + Methotrexate + Fluorouracil | Improved RR, RFS, and OS | Rapid bone loss | [31ā33] |
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OS: overall survival; PFS: progression-free survival; RFS: relapse-free survival; RR: response rate; TTP: time to progression.
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