Drug intelligence / Profile preview

estramustine + docetaxel + carboplatin

Development stage
Phase 2
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

A multi-agent chemotherapy regimen combining the small molecules estramustine, docetaxel, and carboplatin, used investigationally for castration-resistant/hormone-refractory prostate cancer. Estramustine is an estradiol–nitrogen mustard conjugate that disrupts microtubule dynamics and has antiandrogenic/estrogenic effects; docetaxel is a taxane that stabilizes microtubules and inhibits depolymerization; carboplatin is a platinum compound causing DNA crosslinks and apoptosis. The combination (often termed DEC) has shown PSA declines and objective responses with acceptable toxicity when supported with G-CSF in phase II settings for hormone-refractory prostate carcinoma, with reported median time to progression around 8–12 months and overall survival around 19–26 months in earlier-line studies, and shorter outcomes in later-line use.[1][2][5]

Other names
estramustine phosphate + docetaxel + carboplatin
02

Targets

DNAER (Estrogen receptor)TUBB (Tubulin (alpha and beta subunits))

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