Journal of Clinical Oncology · 2008 · 21 citations · 0 references
MedicineOncologyPharmacologyChemotherapyMetastasisOncology PharmacotherapyGenitourinary Cancer PharmacotherapyMetastatic Cancer ManagementMetastatic Disease TreatmentProstate CancerResponse AssessmentTherapy Response AssessmentAdvanced Prostate Cancer TherapyChemotherapy For Prostate CancerPharmacodynamics Of AnalgesicsProgressive Disease AssessmentProgressive Disease QuantificationProstate Cancer Hormonal TherapyStudy PhaseTaxane Resistance
5166 Background: Reliably effective chemotherapy for patients (pts) with HRPC who have progressed after docetaxel remains to be identified. Patupilone is an epothilone with broad spectrum pre-clinical activity including in taxane resistant models. Methods: Multi-center, 2-stage design. Pts with metastatic HRPC with progressive disease documented within 6 months of or while receiving docetaxel were eligible. Patupilone was initially given 10 mg/m2 IV every 3 weeks. PSA response (≥50% decline from baseline) was the primary endpoint. Forty-three pts were to be accrued to stage 1 (H0: response rate <15%, H1: PSA response rate > 25%) and continue to stage 2 if > 6 responses seen. Secondary measures of outcome included progression free and overall survival, measurable disease response, and serial pain and analgesics scores. Results: To date, 33 pts have been enrolled with data available on 19 receiving a median of 4 cycles (range 1–7). Baseline characteristics (range): median age 66 (53–78), PSA 248 (17–1170), hemoglobin 114 (94–149), median time from last docetaxel 4.8 months (1.4–15.0), number of prior chemotherapy regimens 1:2:3+ in 5:10:4 pts, ECOG PS 0:1:2 in 3:12:4 pts, disease in bone, lymph nodes and viscera in 18, 13 and 4 pts respectively. Four first cycle gastrointestinal serious adverse events occurred in the first 6 pts (diarrhea and vomiting) and the dose of patupilone was lowered to 8 mg/m2 for subsequent patients with better tolerance. Grade 3/4 related adverse events at the 8 mg/m2 dose (13 pts): fatigue (1 pt), diarrhea (2 pts) and abdominal pain (1 pt). There have been no grade 3/4 hematologic adverse events. Thus far, PSA declines of ≥30% and ≥50% have occurred in 12/19 (63%) and 8/19 (42%) pts with a confirmed PSA response occurring in 5 pts (26%). Three pts (16%) have had PSA progression as best response. Of 8 pts with evaluable measurable disease, 7 (88%) have had stable disease and 1 pt has had progression as best response. Conclusions: In this population, patupilone 8 mg/m2 every 3 weeks is well tolerated. Initial results show encouraging PSA responses in pts with docetaxel resistant/refractory disease and accrual continues. Author Disclosure Employment or Leadership Consultant or Advisory Role Stock Ownership Honoraria Research Expert Testimony Other Remuneration Novartis