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. Author manuscript; available in PMC: 2016 Dec 16.
Published in final edited form as: Am J Obstet Gynecol. 2011 Jun 24;205(6):535.e1–535.e5. doi: 10.1016/j.ajog.2011.06.067

Table 1.

Participant characteristics at time of random assignment for women with an intact uterus at entry in the NSABP STAR/P-2 trial

Participant Characteristic Tamoxifen (n = 4739) Raloxifene (n = 4717)


No. % No. % P
Age (years)
 ≤ 49 237 5.0 233 4.9 0.99
 50–59 2592 54.7 2584 54.8
 60–69 1516 32.0 1515 32.1
 ≥ 70 394 8.3 385 8.2
Mean (SD) 58.8 (6.8) 58.8 (6.8)
Parity
 ≤ 1 1252 26.4 1211 25.7 0.41
 ≥ 2 3487 73.6 3506 74.3
History of oral contraceptive use
 No 1501 31.7 1540 32.6 0.31
 Yes 3238 68.3 3177 67.4
History of estrogen therapy
 No 1763 37.2 1823 38.6 0.15
 Yes 2976 62.8 2894 61.4
No. of relatives with breast cancer
 0 1489 31.4 1446 30.7 0.22
 1 2399 50.6 2404 51.0
 2 710 15.0 752 15.9
 3 or more 141 3.0 115 2.4
History of diabetes
 Yes 241 5.1 227 4.8 0.54
 No 4498 94.9 4490 95.2
History of hypertension
 Yes 1417 29.9 1383 29.3 0.54
 No 3322 70.1 3334 70.7
Smoking status
 Never 2414 50.9 2448 51.9 0.29
 Former 1860 39.2 1780 37.7
 Current 443 9.3 458 9.7
 Unknown 22 0.5 31 0.7
BMI*
 <25.0 1619 34.2 1576 33.4 0.74
 25.0 – 29.9 1638 34.6 1646 34.9
 ≥ 30.0 1481 31.3 1494 31.7
Mean (SD) 28.1(6.0) 28.2 (6.1)
*

BMI was unavailable for one person in the tamoxifen group and one person in the raloxifene group.