TY - JOUR
T1 - Characterizations of Clinical and Therapeutic Histories for Men with Prostate Cancer-Specific Mortality
AU - Steinberger, Allie E.
AU - Ledet, Elisa M.
AU - Luk, Eric
AU - Cotogno, Patrick
AU - Stolten, Michael
AU - Desmond, Daniel
AU - Feibus, Allison
AU - Silberstein, Jonathan
AU - Sartor, Oliver
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Background Careful descriptions of men with prostate cancer (PCA)-specific mortality are scant in nontrial settings. The present retrospective review describes the clinical characteristics, timelines, and treatment histories from initial presentation to death in a cohort of men with metastatic, castrate-resistant PCA (mCRPC). Unique to the present study is the unequivocal attribution of PCA death by a single experienced clinician. Patients and Methods A total of 119 patients who had been treated at Tulane Cancer Center and had died of mCRPC from 2008 to 2015 were studied through a retrospective review of the medical records. Results The median age at diagnosis was 65 years (range, 40-85 years), and 34.4% of the patients presented with metastatic disease (stage M1). Of these patients, 56% had received definitive primary therapy, all had received androgen-deprivation therapy, and 52% had received docetaxel. The patients had received a median of 7 (1-14) systemic therapies before death. Most were secondary hormonal manipulations after the diagnosis of mCRPC (median, 4; range, 0-9). The median survival was 69 months (range, 5-270 months) after diagnosis, and the median age at death was 73 years (range, 47-95 years). The presence of metastases at diagnosis was a significant predictor of early death (hazard ratio, 4.33; P <.001), and definitive primary therapy was a significant predictor of longer survival (P <.001). The median survival for patients presenting with metastases was 39 months (range, 5-235 months) compared with 100 months (range, 6-270 months) for those with localized disease (P <.001). The median age at diagnosis between the docetaxel- and non-docetaxel-treated patients was significantly different at 62 and 71 years, respectively (P =.002). Conclusion The present retrospective analysis provides initial views clarifying the clinical characteristics of men dying of mCRPC and the therapies they received before death. Additional data are needed in multi-institutional settings to confirm these findings.
AB - Background Careful descriptions of men with prostate cancer (PCA)-specific mortality are scant in nontrial settings. The present retrospective review describes the clinical characteristics, timelines, and treatment histories from initial presentation to death in a cohort of men with metastatic, castrate-resistant PCA (mCRPC). Unique to the present study is the unequivocal attribution of PCA death by a single experienced clinician. Patients and Methods A total of 119 patients who had been treated at Tulane Cancer Center and had died of mCRPC from 2008 to 2015 were studied through a retrospective review of the medical records. Results The median age at diagnosis was 65 years (range, 40-85 years), and 34.4% of the patients presented with metastatic disease (stage M1). Of these patients, 56% had received definitive primary therapy, all had received androgen-deprivation therapy, and 52% had received docetaxel. The patients had received a median of 7 (1-14) systemic therapies before death. Most were secondary hormonal manipulations after the diagnosis of mCRPC (median, 4; range, 0-9). The median survival was 69 months (range, 5-270 months) after diagnosis, and the median age at death was 73 years (range, 47-95 years). The presence of metastases at diagnosis was a significant predictor of early death (hazard ratio, 4.33; P <.001), and definitive primary therapy was a significant predictor of longer survival (P <.001). The median survival for patients presenting with metastases was 39 months (range, 5-235 months) compared with 100 months (range, 6-270 months) for those with localized disease (P <.001). The median age at diagnosis between the docetaxel- and non-docetaxel-treated patients was significantly different at 62 and 71 years, respectively (P =.002). Conclusion The present retrospective analysis provides initial views clarifying the clinical characteristics of men dying of mCRPC and the therapies they received before death. Additional data are needed in multi-institutional settings to confirm these findings.
KW - Castrate-resistant
KW - Longitudinal
KW - Metastatic
KW - Mortality
KW - Prostate cancer
UR - https://www.scopus.com/pages/publications/84960381948
U2 - 10.1016/j.clgc.2015.11.003
DO - 10.1016/j.clgc.2015.11.003
M3 - Article
C2 - 26703881
AN - SCOPUS:84960381948
SN - 1558-7673
VL - 14
SP - 139
EP - 148
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 2
ER -