TY - JOUR
T1 - Early Mortality in Patients With Muscle-Invasive Bladder Cancer Undergoing Cystectomy in the United States
AU - Marqueen, Kathryn E.
AU - Waingankar, Nikhil
AU - Sfakianos, John P.
AU - Mehrazin, Reza
AU - Niglio, Scot A.
AU - Audenet, François
AU - Jia, Rachel
AU - Mazumdar, Madhu
AU - Ferket, Bart S.
AU - Galsky, Matthew D.
N1 - Funding Information:
This work was supported by the National Cancer Institute at the National Institutes of Health (P30 CA196521–01 to MDG, BSF, MM, RJ); the Biostatistics Shared Resource Facility, Icahn School of Medicine at Mount Sinai (MM, RJ, BSF); the American Heart Association (#16MCPRP31030016 to BSF); and the Alpha Omega Alpha Honor Medical Society (2017 Carolyn L. Kuckein Student Research Fellowship to KEM).
Publisher Copyright:
© The Author(s) 2019.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Background: Although radical cystectomy (RC) is a standard treatment for muscle-invasive bladder cancer (MIBC), for many patients the risks versus benefits of RC may favor other approaches. We sought to define the landscape of early postcystectomy mortality in the United States and identify patients at high risk using pretreatment variables. Methods: We identified patients with MIBC (cT2-T4aN0M0) who underwent RC without perioperative chemotherapy within the National Cancer Database (2003–2012). Using multistate multivariable modeling, we calculated time spent in three health states: hospitalized, discharged, and death more than 90 days postcystectomy. Cross-validation was performed by geographic region. Time spent in each state was weighted by utility to determine 90-day quality-adjusted life days (QALDs). Results: Among 7922 patients, 90-day mortality was 7.6% (8.0% for lower and 6.7% for higher volume hospitals). Increasing age, clinical T stage, Charlson Comorbidity Index, and lower volume were associated with higher 90-day mortality and were included in the model. Cross-validation revealed appropriate performance (C-statistics of 0.53–0.74; calibration slopes of 0.50–1.67). The model predicted 25% of patients had a 90-day mortality risk higher than 10%, and observed 90-day mortality in this group was 14.0% (95% CI = 12.5% to 15.6%). Mean quality-adjusted life days (QALDs) was 63 (range = 44–68). Conclusions: RC is associated with relatively high early mortality risk. Pretreatment variables may identify patients at particularly high risk, which may inform clinical trial design, facilitate shared decision making, and enhance quality improvement initiatives.
AB - Background: Although radical cystectomy (RC) is a standard treatment for muscle-invasive bladder cancer (MIBC), for many patients the risks versus benefits of RC may favor other approaches. We sought to define the landscape of early postcystectomy mortality in the United States and identify patients at high risk using pretreatment variables. Methods: We identified patients with MIBC (cT2-T4aN0M0) who underwent RC without perioperative chemotherapy within the National Cancer Database (2003–2012). Using multistate multivariable modeling, we calculated time spent in three health states: hospitalized, discharged, and death more than 90 days postcystectomy. Cross-validation was performed by geographic region. Time spent in each state was weighted by utility to determine 90-day quality-adjusted life days (QALDs). Results: Among 7922 patients, 90-day mortality was 7.6% (8.0% for lower and 6.7% for higher volume hospitals). Increasing age, clinical T stage, Charlson Comorbidity Index, and lower volume were associated with higher 90-day mortality and were included in the model. Cross-validation revealed appropriate performance (C-statistics of 0.53–0.74; calibration slopes of 0.50–1.67). The model predicted 25% of patients had a 90-day mortality risk higher than 10%, and observed 90-day mortality in this group was 14.0% (95% CI = 12.5% to 15.6%). Mean quality-adjusted life days (QALDs) was 63 (range = 44–68). Conclusions: RC is associated with relatively high early mortality risk. Pretreatment variables may identify patients at particularly high risk, which may inform clinical trial design, facilitate shared decision making, and enhance quality improvement initiatives.
UR - http://www.scopus.com/inward/record.url?scp=85070701917&partnerID=8YFLogxK
U2 - 10.1093/JNCICS/PKY075
DO - 10.1093/JNCICS/PKY075
M3 - Article
C2 - 30734024
AN - SCOPUS:85070701917
SN - 2515-5091
VL - 2
JO - JNCI Cancer Spectrum
JF - JNCI Cancer Spectrum
IS - 4
M1 - pky075
ER -