TY - JOUR
T1 - The impact of squamous histology on survival in patients with muscle-invasive bladder cancer
AU - Matulay, Justin T.
AU - Woldu, Solomon L.
AU - Lim, Amy
AU - Narayan, Vikram M.
AU - Li, Gen
AU - Kamat, Ashish M.
AU - Anderson, Christopher B.
N1 - Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/6
Y1 - 2019/6
N2 - Background: Bladder cancer is the ninth most common noncutaneous malignancy worldwide, though a fraction (2%–5%)are diagnosed as squamous cell carcinoma (SCC)in the Western world. Current understanding is based on small, single-institution studies and SEER-database reviews with conflicting results. We used the National Cancer Database to explore clinical characteristics and outcomes from a large cohort of invasive bladder SCC. Methods: We queried the National Cancer Database for diagnoses of urothelial carcinoma (UC)or SCC using International Classification of Disease-O-3 morphologic codes from cases reported between 2004 and 2015. Primary outcome was overall survival in cT2-4N0M0 bladder cancer. Statistical analysis performed using chi-squared test, Kaplan-Meier survival, binomial logistic regression, and Cox proportional hazards. Results: The final cohort included 394,979 bladder cancer patients, of which 4,783 (1.2%)were classified as SCC histology. In comparison to UC, patients with SCC were more likely female (49% vs. 24%; P < 0.01)and African American (11% vs. 5%; P < 0.01). Patients with SCC presented at a higher stage than UC with muscle-invasive bladder cancer (MIBC)present at diagnosis in 70% vs. 19%. On multivariate analysis, SCC independently predicted poorer prognosis (hazard-ratio [HR]1.79, P < 0.01)when controlling for patient characteristics and treatment modality. Unlike UC, there was no benefit with the use of NAC over radical cystectomy alone (HR 0.93, P = 0.69)for patients with SCC. Conclusions: Invasive SCC of the bladder carries a worse prognosis as compared to UC histology, both overall and on a stage-for-stage basis. As opposed to UC, we did not observe a survival benefit for NAC among SCC patients treated with cystectomy.
AB - Background: Bladder cancer is the ninth most common noncutaneous malignancy worldwide, though a fraction (2%–5%)are diagnosed as squamous cell carcinoma (SCC)in the Western world. Current understanding is based on small, single-institution studies and SEER-database reviews with conflicting results. We used the National Cancer Database to explore clinical characteristics and outcomes from a large cohort of invasive bladder SCC. Methods: We queried the National Cancer Database for diagnoses of urothelial carcinoma (UC)or SCC using International Classification of Disease-O-3 morphologic codes from cases reported between 2004 and 2015. Primary outcome was overall survival in cT2-4N0M0 bladder cancer. Statistical analysis performed using chi-squared test, Kaplan-Meier survival, binomial logistic regression, and Cox proportional hazards. Results: The final cohort included 394,979 bladder cancer patients, of which 4,783 (1.2%)were classified as SCC histology. In comparison to UC, patients with SCC were more likely female (49% vs. 24%; P < 0.01)and African American (11% vs. 5%; P < 0.01). Patients with SCC presented at a higher stage than UC with muscle-invasive bladder cancer (MIBC)present at diagnosis in 70% vs. 19%. On multivariate analysis, SCC independently predicted poorer prognosis (hazard-ratio [HR]1.79, P < 0.01)when controlling for patient characteristics and treatment modality. Unlike UC, there was no benefit with the use of NAC over radical cystectomy alone (HR 0.93, P = 0.69)for patients with SCC. Conclusions: Invasive SCC of the bladder carries a worse prognosis as compared to UC histology, both overall and on a stage-for-stage basis. As opposed to UC, we did not observe a survival benefit for NAC among SCC patients treated with cystectomy.
KW - Invasive bladder cancer
KW - Neoadjuvant chemotherapy
KW - Squamous cell carcinoma
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U2 - 10.1016/j.urolonc.2019.01.020
DO - 10.1016/j.urolonc.2019.01.020
M3 - Article
C2 - 30704959
AN - SCOPUS:85060527564
SN - 1078-1439
VL - 37
SP - 353.e17-353.e24
JO - Urologic Oncology: Seminars and Original Investigations
JF - Urologic Oncology: Seminars and Original Investigations
IS - 6
ER -