TY - JOUR
T1 - Localized prostate cancer
T2 - An analysis of the CDC Breast and Prostate Cancer Data Quality and Patterns of Care study (CDC PoC-BP)
AU - Celtik, Kenan
AU - Wallis, Christopher J.D.
AU - Lo, Mary
AU - Lim, Kelvin
AU - Lipscomb, Joseph
AU - Fleming, Steven
AU - Wu, Xiao Cheng
AU - Anderson, Roger T.
AU - Thompson, Trevor D.
AU - Farach, Andrew
AU - Hamilton, Ann S.
AU - Miles, Brian J.
AU - Satkunasivam, Raj
N1 - Funding Information:
We utilized the CDC PoC-BP dataset of 8,229 men diagnosed with histologically confirmed localized PCa in 2004 from seven state cancer registries funded by CDC’s National Program of Cancer Registries. The sampling methods employed have been previously described and included data abstraction from hospitals and non-hospitals (e.g. office and radiation facility) between 2007-2009.12 State cancer registries provided vital status, date of death or last date of contact, and ICD codes for cause of death as of December 31, 2015. Analysis was restricted to patients receiving definitive treatment within 6 months of diagnosis (57% of the cohort) as those receiving treatment after 6 months likely represents management with active surveillance. Further, we excluded patients treated with conservative therapies (active surveillance, expectant management, or primary androgen deprivation therapy), combination brachytherapy +/-IMRT, other forms of EBRT, ablation therapy, and other nonradical extirpative treatments. We identified 3019 patients who underwent RP (open and minimally invasive approaches, which have demonstrably comparable oncologic outcomes13) and 667 patients treated IMRT.
Funding Information:
Funding: The Hamill Foundation. The Breast and Prostate Cancer Data Quality and Patterns of Care study was supported by the Centers for Disease Control and Prevention through cooperative agreements with the California Cancer Registry (Public Health Institute) (1-U01-DP000260), Emory University (1-U01-DP000258), Louisiana State University Health Sciences Center (1-U01-DP000253), Minnesota Cancer Surveillance System (Minnesota Department of Health) (1-U01-DP000259), Medical College of Wisconsin (1-U01-DP000261), University of Kentucky (1-U01-DP000251), and Wake Forest University (1-U01-DP000264). The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.
Publisher Copyright:
© 2022 Canadian Urological Association.
PY - 2022/7
Y1 - 2022/7
N2 - Introduction: Limited evidence exists on the comparative effectiveness of local treatments for prostate cancer (PCa) due to the lack of generalizability. Using granular national data, we sought to examine the association between radical prostatectomy (RP) and intensity-modulated radiation therapy (IMRT) treatment and survival. Methods: Records were abstracted for localized PCa cases diagnosed in 2004 across seven state registries to identify patients undergoing RP (n=3019) or IMRT (n=667). Comorbidity was assessed by the Adult Comorbidity Evaluation-27 (ACE-27). Propensity score matching (PSM) was used to balance covariates between treatment groups. All-cause and PCa-specific mortality were primary endpoints. A subgroup analysis of patients with high-risk PCa (RP, n=89; IMRT, n=95) was conducted. Results: Following PSM, matched patients (n=502 pairs) treated with either RP or IMRT were well-balanced with respect to covariates. With a median followup of 10.5 years (interquartile range [IQR] 9.9-11.0), the 11-year overall survival (OS) was 71.2% (95% confidence interval [CI] 66.9-75.8) for RP and 62.3% (95% CI 57.4-67.6) for IMRT. IMRT was associated with a 41% increased risk of all-cause mortality (hazard ratio [HR] 1.41, 95% CI 1.13-1.76) but not PCa-specific mortality (HR 1.75, 95% CI 0.84-3.64), as compared to RP. In patients with highrisk PCa, IMRT, as compared to RP, was not associated with statistically significant difference in all-cause (HR 1.53, 95% CI 0.97-2.42) or PCa-specific mortality (HR 1.92, 95% CI 0.69- 5.36). Conclusions: Despite a low mortality rate at 10 years and possible residual confounding, we found a significantly increased risk of all-cause mortality, but no PCa-specific mortality associated with IMRT as compared to RP in this population-based study.
AB - Introduction: Limited evidence exists on the comparative effectiveness of local treatments for prostate cancer (PCa) due to the lack of generalizability. Using granular national data, we sought to examine the association between radical prostatectomy (RP) and intensity-modulated radiation therapy (IMRT) treatment and survival. Methods: Records were abstracted for localized PCa cases diagnosed in 2004 across seven state registries to identify patients undergoing RP (n=3019) or IMRT (n=667). Comorbidity was assessed by the Adult Comorbidity Evaluation-27 (ACE-27). Propensity score matching (PSM) was used to balance covariates between treatment groups. All-cause and PCa-specific mortality were primary endpoints. A subgroup analysis of patients with high-risk PCa (RP, n=89; IMRT, n=95) was conducted. Results: Following PSM, matched patients (n=502 pairs) treated with either RP or IMRT were well-balanced with respect to covariates. With a median followup of 10.5 years (interquartile range [IQR] 9.9-11.0), the 11-year overall survival (OS) was 71.2% (95% confidence interval [CI] 66.9-75.8) for RP and 62.3% (95% CI 57.4-67.6) for IMRT. IMRT was associated with a 41% increased risk of all-cause mortality (hazard ratio [HR] 1.41, 95% CI 1.13-1.76) but not PCa-specific mortality (HR 1.75, 95% CI 0.84-3.64), as compared to RP. In patients with highrisk PCa, IMRT, as compared to RP, was not associated with statistically significant difference in all-cause (HR 1.53, 95% CI 0.97-2.42) or PCa-specific mortality (HR 1.92, 95% CI 0.69- 5.36). Conclusions: Despite a low mortality rate at 10 years and possible residual confounding, we found a significantly increased risk of all-cause mortality, but no PCa-specific mortality associated with IMRT as compared to RP in this population-based study.
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U2 - 10.5489/cuaj.7580
DO - 10.5489/cuaj.7580
M3 - Article
AN - SCOPUS:85131053844
VL - 16
JO - Journal of the Canadian Urological Association
JF - Journal of the Canadian Urological Association
SN - 1911-6470
IS - 7
ER -