Incidence, Characteristics and Survival Rates of Bladder Cancer after Rectosigmoid Cancer Radiation

Author:

Angelis Mario de123ORCID,Siech Carolin14ORCID,Di Bello Francesco15ORCID,Peñaranda Natali Rodriguez16ORCID,Goyal Jordan A.1,Tian Zhe1,Longo Nicola5,Chun Felix K. H.4,Puliatti Stefano6,Saad Fred1ORCID,Shariat Shahrokh F.78910,Longoni Mattia23ORCID,Gandaglia Giorgio23,Moschini Marco23,Montorsi Francesco23,Briganti Alberto23,Karakiewicz Pierre I.1

Affiliation:

1. Cancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, QC H2X 3E4, Canada

2. Division of Experimental Oncology, Unit of Urology, URI, IRCCS Ospedale San Raffaele, 20132 Milan, Italy

3. Vita-Salute San Raffaele University, 20132 Milan, Italy

4. Department of Urology, University Hospital, Goethe University Frankfurt, 60590 Frankfurt am Main, Germany

5. Department of Neurosciences, Science of Reproduction and Odontostomatology, University of Naples Federico II, 80131 Naples, Italy

6. Department of Urology, Ospedale Policlinico e Nuovo Ospedale Civile S. Agostino Estense Modena, University of Modena and Reggio Emilia, 41121 Modena, Italy

7. Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, 1090 Vienna, Austria

8. Department of Urology, Weill Cornell Medical College, New York, NY 10065, USA

9. Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

10. Hourani Center of Applied Scientific Research, Al-Ahliyya Amman University, Amman 19328, Jordan

Abstract

Background: Historical external beam radiation therapy (EBRT) for rectosigmoid cancer (RCa) predisposed patients to an increased risk of secondary bladder cancer (BCa). However, no contemporary radiotherapy studies are available. We addressed this knowledge gap. Materials and methods: Within the Surveillance, Epidemiology, and End Results database (2000–2020), we identified non-metastatic RCa patients who either underwent radiotherapy (EBRT+) or did not (EBRT-). Cumulative incidence plots and multivariable competing risk regression models (CRR) were fitted to address rates of BCa after RCa. In the subgroup of BCa patients, the same methodology addressed BCa-specific mortality (BCSM) according to EBRT exposure status. Results: Of the 188,658 non-metastatic RCa patients, 54,562 (29%) were EBRT+ vs. 134,096 (73%) who were EBRT-. In the cumulative incidence plots, the ten-year BCa rates were 0.7% in EBRT+ vs. 0.7% in EBRT- patients (p = 0.8). In the CRR, EBRT+ status was unrelated to BCa rates (multivariable HR: 1.1, p = 0.8). In the subgroup of 1416 patients with BCa after RCa, 443 (31%) were EBRT+ vs. 973 (69%) who were EBRT-. In the cumulative incidence plots, the ten-year BCSM rates were 10.6% in EBRT+ vs. 12.1% in EBRT- patients (p = 0.7). In the CRR, EBRT+ status was unrelated to subsequent BCSM rates (multivariable HR: 0.9, p = 0.9). Conclusion: Although historical EBRT for RCa predisposed patients to higher BCa rates, contemporary EBRT for RCa is not associated with increased subsequent BCa risk. Moreover, in patients with BCa after RCa, exposure to EBRT does not affect BCSM.

Publisher

MDPI AG

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