TY - JOUR
T1 - Clinical Stage Migration and Survival for Renal Cell Carcinoma in the United States
AU - Patel, Hiten D.
AU - Gupta, Mohit
AU - Joice, Gregory A.
AU - Srivastava, Arnav
AU - Alam, Ridwan
AU - Allaf, Mohamad E.
AU - Pierorazio, Phillip M.
N1 - Publisher Copyright:
© 2018 European Association of Urology
PY - 2019/7
Y1 - 2019/7
N2 - Background: The rising incidence of renal cell carcinoma (RCC) since the 1980s has been accompanied by stage migration toward early-stage (stage I) cancers. Stage migration drove an apparent increase in survival for RCC since the 1980s, but it is unclear whether it remains a contributor more recently. Objective: To determine whether clinical stage migration has persisted and the relative impact of stage migration versus improvements in treatment on survival for RCC. Design, setting, and participants: An epidemiologic assessment of stage migration and survival for 262 597 patients at diagnosis of RCC (2004–2015) across >1500 facilities in the National Cancer Database. Outcome measurements and statistical analysis: Proportion of patients over time was assessed by clinical stage at diagnosis via Cochran-Armitage chi-square tests and linear regression. Mortality data were assessed with the Kaplan-Meier method for 5-yr overall survival, Cox proportional hazards regression, and propensity score matching to differentiate the impact of treatment including systemic therapy from stage migration. Results and limitations: Greater diagnosis of clinical stage I disease (70%; p < 0.001) was observed, with decreased diagnosis of stage III (8%; p < 0.001) and stage IV (11%; p < 0.001) up to 2007 followed by stabilization through 2015. Tumor size continues to decrease for localized tumors (mean–0.22 cm stage I and–1.24 cm stage II, 2004–2015). Histology demonstrated significant associations with stage. Five-year overall survival improved (67.9% [2004] to 72.3% [2010]) with gains in advanced RCC but not localized tumors. Models confirmed improved survival in recent years for stage IV patients. Systemic therapy was associated with improved survival (hazard ratio 0.811 [0.786–0.837], p < 0.001). National Cancer Database limitations apply. Conclusions: The proportion of patients presenting with stage I RCC has stabilized (70%), suggesting that stage migration may have ended. Localized tumors are detected with decreasing size, while advanced cancers have remained stable. Only 11% of patients now present with distant metastatic disease, but 5-yr overall survival is improving in recent years due to improved treatments rather than stage migration. Patient summary: In this study, we found that stage migration toward early-stage cancers has ended for renal cell carcinoma (RCC). However, improved treatment for advanced RCC appears to be responsible for improved survival in recent years.
AB - Background: The rising incidence of renal cell carcinoma (RCC) since the 1980s has been accompanied by stage migration toward early-stage (stage I) cancers. Stage migration drove an apparent increase in survival for RCC since the 1980s, but it is unclear whether it remains a contributor more recently. Objective: To determine whether clinical stage migration has persisted and the relative impact of stage migration versus improvements in treatment on survival for RCC. Design, setting, and participants: An epidemiologic assessment of stage migration and survival for 262 597 patients at diagnosis of RCC (2004–2015) across >1500 facilities in the National Cancer Database. Outcome measurements and statistical analysis: Proportion of patients over time was assessed by clinical stage at diagnosis via Cochran-Armitage chi-square tests and linear regression. Mortality data were assessed with the Kaplan-Meier method for 5-yr overall survival, Cox proportional hazards regression, and propensity score matching to differentiate the impact of treatment including systemic therapy from stage migration. Results and limitations: Greater diagnosis of clinical stage I disease (70%; p < 0.001) was observed, with decreased diagnosis of stage III (8%; p < 0.001) and stage IV (11%; p < 0.001) up to 2007 followed by stabilization through 2015. Tumor size continues to decrease for localized tumors (mean–0.22 cm stage I and–1.24 cm stage II, 2004–2015). Histology demonstrated significant associations with stage. Five-year overall survival improved (67.9% [2004] to 72.3% [2010]) with gains in advanced RCC but not localized tumors. Models confirmed improved survival in recent years for stage IV patients. Systemic therapy was associated with improved survival (hazard ratio 0.811 [0.786–0.837], p < 0.001). National Cancer Database limitations apply. Conclusions: The proportion of patients presenting with stage I RCC has stabilized (70%), suggesting that stage migration may have ended. Localized tumors are detected with decreasing size, while advanced cancers have remained stable. Only 11% of patients now present with distant metastatic disease, but 5-yr overall survival is improving in recent years due to improved treatments rather than stage migration. Patient summary: In this study, we found that stage migration toward early-stage cancers has ended for renal cell carcinoma (RCC). However, improved treatment for advanced RCC appears to be responsible for improved survival in recent years.
KW - Kidney cancer
KW - Renal cell carcinoma
KW - Small renal mass
KW - Stage migration
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U2 - 10.1016/j.euo.2018.08.023
DO - 10.1016/j.euo.2018.08.023
M3 - Article
C2 - 31277771
AN - SCOPUS:85065958444
SN - 2588-9311
VL - 2
SP - 343
EP - 348
JO - European Urology Oncology
JF - European Urology Oncology
IS - 4
ER -