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. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2019 Dec 23;29(2):520–523. doi: 10.1158/1055-9965.EPI-19-1079

Table 1.

Patient characteristics of study population by concomitant hydrochlorothiazide exposure

HCTZ, N (%) No HCTZ, N (%)
Total 581 1555
Age at diagnosis (mean (SD)) 71.5 (4.5) 71.2 (4.4)
Age category
 66-69 years 236 (40.2) 681 (43.8)
 70-74 years 211 (35.7) 539 (34.7)
 75-79 years 97 (17.3) 249 (16.0)
 80+ years 37 (6.4) 86 (5.5)
Race
 White 455 (78.3) 1308 (84.1)
 Black 87 (15.0) 128 (8.2)
 Other 39 (6.7) 119 (7.7)
Stage at diagnosis
 I 133 (22.9) 359 (23.1)
 II 328 (56.5) 826 (53.1)
 III 120 (20.7) 370 (23.8)
Charlson Comorbidity Score
 0 333 (57.3) 970 (62.4)
 1 164 (28.2) 386 (24.8)
 2+ 84 (14.5) 199 (12.8)
Regimen*
 TC 295 (50.8) 824 (53.0)
 AC 54 (9.3) 165 (10.6)
 CMF 48 (8.3) 111 (7.1)
 DD-AC 148 (25.5) 365 (23.5)
 Other 36 (6.2) 90 (5.8)
Colony stimulating factor (CSF)
 No 193 (33.2) 510 (32.8)
 Yes 388 (66.8) 1045 (67.2)
*

Regimens include TC (docetaxel + cyclophosphamide or paclitaxel + cyclophosphamide or paclitaxel + docetaxel + cyclophosphamide), AC (doxorubicin + cyclophosphamide), CMF (cyclophosphamide (oral) + methotrexate + fluorouracil), dose-dense AC (doxorubicin + cyclophosphamide + colony stimulating factor), and Other which includes EC (epirubicin + cyclophosphamide), TAC (docetaxel + doxorubicin + cyclophosphamide), and CEF (cyclophosphamide + epirubicin + fluorouracil).