scholarly journals Taxanes for the Treatment of Metastatic Breast Cancer

2012 ◽  
Vol 6 ◽  
pp. BCBCR.S8205 ◽  
Author(s):  
W.J. Gradishar

Taxanes have remained a cornerstone of breast cancer treatment over the past three decades, improving the lives of patients with both early- and late-stage disease. The purpose of this review is to summarize the current role of taxanes, including an albumin-bound formulation that enhances delivery of paclitaxel to tumors, in the management of metastatic breast cancer (MBC). Since the introduction of Cremophor EL-paclitaxel to the clinic in the mid-1990s, a substantial amount of investigation has gone into subjects such as formulation, dose, schedule, and taxane resistance, allowing physicians greater flexibility in treating patients with MBC. This review will also examine how the shrinking pool of taxane-naive patients, a result of the expansion of taxanes into the neoadjuvant and adjuvant settings, will respond to taxane retreatment for metastatic disease. Taxane treatment seems likely to continue to play an important role in the treatment of MBC.


2016 ◽  
Vol 49 (12) ◽  
pp. 970-972
Author(s):  
Arkadius Polasik ◽  
Thomas W. P. Friedl ◽  
Amelie Schramm ◽  
Fabienne Schochter ◽  
Jens Huober ◽  
...  


2016 ◽  
Vol 49 (9) ◽  
pp. 680-684
Author(s):  
Arkadius Polasik ◽  
Thomas W. P. Friedl ◽  
Amelie Schramm ◽  
Fabienne Schochter ◽  
Jens Huober ◽  
...  


Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1488
Author(s):  
Alessandra Ammazzalorso ◽  
Mariangela Agamennone ◽  
Barbara De Filippis ◽  
Marialuigia Fantacuzzi

The inhibition of cyclin dependent kinases 4 and 6 plays a role in aromatase inhibitor resistant metastatic breast cancer. Three dual CDK4/6 inhibitors have been approved for the breast cancer treatment that, in combination with the endocrine therapy, dramatically improved the survival outcomes both in first and later line settings. The developments of the last five years in the search for new selective CDK4/6 inhibitors with increased selectivity, treatment efficacy, and reduced adverse effects are reviewed, considering the small-molecule inhibitors and proteolysis-targeting chimeras (PROTACs) approaches, mainly pointing at structure-activity relationships, selectivity against different kinases and antiproliferative activity.





2019 ◽  
Vol 43 (5) ◽  
pp. 438-442 ◽  
Author(s):  
Manish Sharma ◽  
Ajay Gogia ◽  
Suryanarayana S.V. Deo ◽  
Sandeep Mathur




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