Secondary primary malignancies among patients with GU cancer.

Authors

null

Nikita Tripathi

Division of Hematology and Medical Oncology, Mayo Clinic, Phoeniz, AZ

Nikita Tripathi , Ahsan Ayaz , Syed Arsalan Ahmed Naqvi , Muhammad Ali Khan , Akshat Saxena , Arifa Bibi , Aneeta Channar , Mark Tyson , Irbaz Bin Riaz , Ewan Kemar Cobran , Alan Haruo Bryce , Haidar Abdul-Muhsin , Parminder Singh

Organizations

Division of Hematology and Medical Oncology, Mayo Clinic, Phoeniz, AZ, Montefiore St. Luke's Cornwall Hospital, Newburgh, NY, Division of Hematology and Medical Oncology, Mayo Clinic, Phoenix, AZ, Division of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, Mayo Clinic Arizona, Phoenix, AZ, Division of Hematology and Oncology, Mayo Clinic, Scottsdale, AZ, Mayo Clinic College of Medicine and Science, Scottsdale, AZ, Mayo Clinic Arizona, Scottsdale, AZ, Department of Oncology, Mayo Clinic, Phoenix, AZ

Research Funding

No funding sources reported

Background: The risk of secondary primary malignancies (SPM) among the survivors of GU cancer is not well-established. In this study, we attempt to describe the patterns of SPMs in patients diagnosed with GU cancers. Methods: The Surveillance, Epidemiology, and End Results (SEER) database (SEER*Stat 8.4.2) was searched to obtain data on the incidence of SPM in adult patients (age >18 years) diagnosed with GU cancers, including prostate, renal, and bladder cancer. Standardized incidence ratios (SIRs) with a 95% confidence interval (CI) were calculated. SIR was defined as the observed SPMS from each category divided by the expected number of SPMs in the age-matched US population for the same period. The data was further stratified by age (<50y, 50-70y, >70y), race (White, Black, Asian/Pacific Islander), ethnicity (Hispanic, non-Hispanic), chemotherapy, and radiotherapy exposure. Results: A total of 1,041,217 patients were included in this analysis. In patients diagnosed with GU cancer, the incidence of overall SPM was 11%. Particularly, patients with GU cancers were observed to have a high incidence of Endocrine system SPM (1.52; 1.45-1.59), and urinary system SPM (1.51; 1.49-1.53) These results were consistent by different sociodemographic groups. In patients diagnosed with prostate cancer, the incidence of thyroid SPM was increased (1.31; 1.23-1.39). Particularly, prostate cancer patients treated with radiation therapy had increased incidence rates of SPM in the peritoneum, omentum and mesentery (1.57; 0.79-2.81) and urinary bladder (1.36;1.32-1.40) was higher as compared to those with no exposure to radiation therapy (1.11;1.08-1.13 and 1.03;1-1.06 respectively). Bladder cancer patients had an overall increased incidence of SPM in the esophagus (1.21; 1.08-1.35), lung, bronchus, trachea, and other respiratory organs (1.97;1.92-2.01), prostate (3.50;3.4-3.6) and kidney (1.86;1.76-1.97). A higher incidence of renal pelvis, ureter and other urinary organ SPM (11.08;10.48-11.07) was also notable in this population. Similarly, kidney cancer patients had a higher incidence of the endocrine system (3.00;2.74-3.27), prostate (1.24;1.2-1.29) and bladder 1.78;1.68-1.79 SPMs. Conclusions: This population-based study shows an increased risk of SPM development in GU cancer survivors compared to the general population. Clinicians should keep a high index of suspicion for SPMs and initiate appropriate workups at early warning signs.

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Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Prostate Cancer

Track

Prostate Cancer - Advanced,Prostate Cancer - Localized

Sub Track

Quality of Care/Quality Improvement and Real-World Evidence

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 98)

DOI

10.1200/JCO.2024.42.4_suppl.98

Abstract #

98

Poster Bd #

D13

Abstract Disclosures

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