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Clinical Trial
. 2009 Jul;182(1):317-23.
doi: 10.1016/j.juro.2009.02.105. Epub 2009 May 17.

Phase II trial of capecitabine and weekly docetaxel for metastatic castrate resistant prostate cancer

Affiliations
Clinical Trial

Phase II trial of capecitabine and weekly docetaxel for metastatic castrate resistant prostate cancer

Ulka N Vaishampayan et al. J Urol. 2009 Jul.

Abstract

Purpose: Synergy is observed with the combination of capecitabine and docetaxel due to docetaxel mediated up-regulation of thymidine phosphorylase. A phase II trial was performed with the combination for metastatic, castrate resistant prostate cancer.

Materials and methods: Eligible patients had metastatic, castrate resistant prostate cancer, no prior chemotherapy for metastatic disease and normal organ function. Docetaxel (36 mg/m(2) per week intravenously) on days 1, 8 and 15, and capecitabine (1,250 mg/m(2) per day in 2 divided doses) on days 5 to 18 were administered in 28-day cycles. The response was assessed every 2 cycles. Biomarker correlative studies were performed on blood dihydropyrimidine dehydrogenase, and the thymidine phosphorylase-to-dihydropyrimidine dehydrogenase and thymidine synthase-to-dihydropyrimidine dehydrogenase ratios in available prostate tumor tissue.

Results: A total of 30 patients with a median age of 69 years were enrolled in the study. We noted bone pain in 21 patients (70%), Gleason score 8 or higher in 18 (60%), measurable disease progression in 9, bone scan progression in 18 and prostate specific antigen progression in 22. Grade 3 or 4 neutropenia was seen in 3 patients and grade 3 hand-foot syndrome was found in 2. No treatment related deaths occurred. A prostate specific antigen response of 50% or greater decrease was observed in 22 patients (73%), of whom 9 (30%) had 90% or greater decrease. A partial response was noted in 5 of 9 patients (56%) with measurable disease. Median time to progression was 6.7 months (90% CI 4.2-7.7) and median overall survival was 22.0 months (90% CI 18.4-25.3).

Conclusions: The combination was well tolerated and it demonstrated favorable response rates with durable remission and survival outcomes.

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Figures

Figure 1
Figure 1
Waterfall plot demonstrates PSA response data, that is percent change from baseline, in all 30 patients (vertical lines). Four patients had no PSA change with 0% change. Rank 1, most negative percent change in PSA.
Figure 2
Figure 2
Kaplan-Meier graph shows 30 patients with metastatic CRPC treated with docetaxel and capecitabine. Tick marks represent 10 censored survivors. Dashed lines indicate 90% CI at successive time points.
Figure 3
Figure 3
Kaplan-Meier graph reveals TTP in 22 patients with metastatic AIPC by median dichotomized tumor tissue TP/DPD ratio. Tick mark represents 1 censored survivor who was progression free. Low, 0.58 or less. High, greater than 0.58. TTP differed significantly between these 2 subgroups (log rank test p = 0.0132).

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