Table 1.
Trial (Reference) | Study Population | Number of Subjects Randomly Assigned | Treatment Groups | Median Treatment Duration (Years) | Primary End Point | RR (95% CI) | |
---|---|---|---|---|---|---|---|
CRC Incidence | CRC-Related Mortality | ||||||
PHS [19] | Male physicians (age 40–84 years) without history of MI, stroke, cancer, liver or renal disease, gout, peptic ulcer or contraindications to aspirin | 22,071 | Placebo versus 325 mg aspirin alternate day | 5.0 | CVD and cancer | 1.03 (0.83–1.28) | Not reported |
WHS [21] | Women (age ≥ 45 years) without history of cancer (except non-melanoma skin cancer), CVD or other major chronic illness | 39,876 | Placebo versus 100 mg aspirin alternate day | 10.1 | CVD and cancer | 0.80 (0.67–0.97) | 0.80 (0.67–0.97) |
BDA [22] | Male physicians without peptic ulcer, stroke or definite MI | 5139 | Placebo versus 500 mg aspirin per day | 6.0 | CVD | 0.70 (0.51–0.97) | 0.73 (0.49–1.10) |
UK-TIA Aspirin Trial [23] | Patients with prior TIA or stroke | 2449 | Placebo versus 300 or 1200 mg aspirin per day | 4.4 | CVD | 0.75 (0.56–0.97), [25] pooled with TPT and SALT | 0.61 (0.43–0.87), [25] pooled with TPT and SALT |
TPT [41] | High risk for IHD | 5085 | Placebo versus 75 mg aspirin per day (alone or with warfarin) | 6.9 | CVD | 0.75 (0.56–0.97), [25] pooled with UK-TIA and SALT | 0.61 (0.43–0.87), [25] pooled with UK-TIA and SALT |
SALT [42] | Prior TIA or stroke or retinal occlusion | 1363 | Placebo versus 75 mg aspirin per day | 2.7 | CVD | 0.75 (0.56–0.97), [25] pooled with TPT and UK-TIA | 0.61 (0.43–0.87), [25] pooled with TPT and UK-TIA |
BDA, British Doctors Aspirin Trial; CI, confidence interval; CRC, colorectal cancer; CVD, cardiovascular disease; IHD, Ischemic heart disease; PHS, Physicians’ Health Study; RR, relative risk; SALT, Swedish Aspirin Low Dose Trial; TIA, Transient Ischaemic Attack; TPT, Thrombosis Prevention Trial; UK-TIA, UK-Transient Ischaemic Attack; WHS, Women’s Health Study.