Therapeutic potential of taxanes in the treatment of metastatic pancreatic cancer
Language English Country Germany Media print-electronic
Document type Journal Article, Review
PubMed
27250969
DOI
10.1007/s00280-016-3058-y
PII: 10.1007/s00280-016-3058-y
Knihovny.cz E-resources
- Keywords
- Docetaxel, Drug resistance, Nab-paclitaxel, Paclitaxel, Pancreatic cancer, Taxane,
- MeSH
- Drug Resistance, Neoplasm MeSH
- Carcinoma, Pancreatic Ductal drug therapy MeSH
- Clinical Trials as Topic MeSH
- Humans MeSH
- Neoplasm Metastasis MeSH
- Pancreatic Neoplasms drug therapy pathology MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Taxoids administration & dosage therapeutic use MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Taxoids MeSH
Most patients with pancreatic ductal adenocarcinoma (PDAC) present with unresectable or metastatic disease with very poor prognosis. Chemotherapy is the primary treatment modality for patients with locally advanced and metastatic PDAC, but the efficacy of currently available regimens is limited. Taxanes are widely used in many primary cancers including breast, ovarian and lung cancers. The activity of combined regimen of taxanes plus nucleoside analogue or platinum derivate in terms of response rate ranges between 20 and 57 % in PDAC and may prolong overall survival. Since 2013 nab-paclitaxel (paclitaxel-albumin-bound particles) became a new treatment option for patients with metastatic pancreatic cancer based on the results of MPACT trial. Moreover, encouraging activity in PDAC of the combination regimen of paclitaxel and carboplatin that is being widely used in other solid tumors has been reported recently. Biomarkers, including biomarkers predictive of taxane resistance, could allow individualized tailored therapy. BRCA mutation status could serve as predictor of better chemotherapy treatment outcome in PDAC. The present review summarizes the principal clinical trials evaluating the efficacy of taxanes both as monotherapy and in combination in view of the potential use in the treatment of PDAC.
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