Research Article

Incidence of Second Primary Malignancies in Patients with Castration-Resistant Prostate Cancer: An Observational Retrospective Cohort Study in the United States

Table 1

Cohort selection.

Reason for exclusionNo. of patients ()Remaining sample

Initial sample of prostate cancer cases from SEER-Medicare data564,491 (100)564,491
No record of surgical or biologic castration383,713 (67.98)180,778
No record of second-line systemic therapy after castration date168,388 (29.83)12,390
Castration was on or before prostate cancer diagnosis date376 (0.07)12,014
Diagnosis of any cancer other than prostate cancer or nonmelanoma skin cancer on or before potential cohort entry date5,543 (0.98)6,471
Diagnostic code for exclusionary metastases (197X or 198X with exception of 198.2-skin or 198.5-bone) on or before potential cohort entry date1,767 (0.31)4,704
Not aged at least 65 years on potential cohort entry date246 (0.04)4,458
Not continuously enrolled in both Parts A and B Medicare coverage between the earlier of (1) 12 months before cohort entry or (2) the month of prostate cancer diagnosis and cohort entry date1,293 (0.23)3,165
Enrolled in HMO either (1) in year before potential cohort entry date, or (2) at some time between diagnosis date of initial prostate cancer identified in SEER and potential cohort entry date931 (0.16)2,234

SEER, Surveillance, Epidemiology, and End Results program of the US National Cancer Institute; HMO, health maintenance organization.
Abiraterone, cabazitaxel, docetaxel, enzalutamide, mitoxantrone, or sipuleucel-T.