TY - JOUR
T1 - Pretreatment neutrophil-to-lymphocyte ratio in metastatic castration-resistant prostate cancer patients treated with ketoconazole
T2 - Association with outcome and predictive nomogram
AU - Keizman, Daniel
AU - Gottfried, Maya
AU - Ish-Shalom, Maya
AU - Maimon, Natalie
AU - Peer, Avivit
AU - Neumann, Avivit
AU - Rosenbaum, Eli
AU - Kovel, Svetlana
AU - Pili, Roberto
AU - Sinibaldi, Victoria
AU - Carducci, Michael A.
AU - Hammers, Hans
AU - Eisenberger, Mario A.
AU - Sella, Avishay
PY - 2012
Y1 - 2012
N2 - Background. The neutrophil-to-lymphocyte ratio (NLR), an inflammation marker, is prognostic in several cancers. We assessed the association between the pretreatment NLR and outcome of patients with metastatic castration-resistant prostate cancer (mCRPC) treated with the CYP17 inhibitor ketoconazole. Methods. This was an international, retrospective study of 156 mCRPC patients treated with ketoconazole. The independent effect of the pretreatment NLR and factors associated with treatment outcome were determined by multivariate analysis. Results. Seventy-eight patients (50%) had a ≥50% decline in prostate-specific antigen (PSA). The median progression-free survival (PFS) time was 8 months. Excluded from the analysis were 23 patients without available data on their NLR and those with a recent health event or treatment associated with a blood count change. Sixty-two patients (47%) had a pretreatment NLR >3. Risk factors associated with the PFS outcome were a pretreatment NLR >3 and PSA doubling time (PSADT) <3 months and a prior response to a gonadotropin-releasing hormone agonist of <24 months or to an antiandrogen of <6 months. The number of risk factors was used to form a predictive nomogram by patient categorization into favorable (zero or one factor), intermediate (two factors), and poor (three or four factors) risk groups. Conclusions. In mCRPC patients treated with ketoconazole, the pretreatment NLR and PSADT, and prior response to androgen-deprivation therapy, may be associated with the PFS time and used to form a risk stratification predictive nomogram.
AB - Background. The neutrophil-to-lymphocyte ratio (NLR), an inflammation marker, is prognostic in several cancers. We assessed the association between the pretreatment NLR and outcome of patients with metastatic castration-resistant prostate cancer (mCRPC) treated with the CYP17 inhibitor ketoconazole. Methods. This was an international, retrospective study of 156 mCRPC patients treated with ketoconazole. The independent effect of the pretreatment NLR and factors associated with treatment outcome were determined by multivariate analysis. Results. Seventy-eight patients (50%) had a ≥50% decline in prostate-specific antigen (PSA). The median progression-free survival (PFS) time was 8 months. Excluded from the analysis were 23 patients without available data on their NLR and those with a recent health event or treatment associated with a blood count change. Sixty-two patients (47%) had a pretreatment NLR >3. Risk factors associated with the PFS outcome were a pretreatment NLR >3 and PSA doubling time (PSADT) <3 months and a prior response to a gonadotropin-releasing hormone agonist of <24 months or to an antiandrogen of <6 months. The number of risk factors was used to form a predictive nomogram by patient categorization into favorable (zero or one factor), intermediate (two factors), and poor (three or four factors) risk groups. Conclusions. In mCRPC patients treated with ketoconazole, the pretreatment NLR and PSADT, and prior response to androgen-deprivation therapy, may be associated with the PFS time and used to form a risk stratification predictive nomogram.
KW - Ketoconazole treatment
KW - Metastatic castration-resistant prostate cancer
KW - Neutrophil-to-lymphocyte ratio
KW - Outcome
KW - Predictive nomogram
UR - http://www.scopus.com/inward/record.url?scp=84871598079&partnerID=8YFLogxK
U2 - 10.1634/theoncologist.2012-0125
DO - 10.1634/theoncologist.2012-0125
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C2 - 22971522
AN - SCOPUS:84871598079
SN - 1083-7159
VL - 17
SP - 1508
EP - 1514
JO - Oncologist
JF - Oncologist
IS - 12
ER -