Included Trials | Stagea non-user/ user | Dosage | Duration | Reason | Outcomes |
---|---|---|---|---|---|
gastric cancer | |||||
Spence et al. [11] 2018 | I 28 (1.5%) 12 (2.4%) II 43 (2.3%) 20 (4.0%) III 59 (3.1%) 16 (3.2%) IV 119 (6.3%) 16 (3.2%) Missing 1646 (86.9%) 432 (87.1%) | Low-dose aspirin (75 mg) use | 182, 365, 548 and 730 tablets | Unknown | not associated with increased survival in sophageal or gastric cancer |
Spence et al. [11] 2018 | Unknown | Low-dose aspirin (75 mg) use | 182, 365, 548 and 730 tablets | Unknown | not associated with increased survival in sophageal or gastric cancer |
Frouws et al. [7] 2017 | Unknown | Nonusers were defined as patients who received for less than 30 days or never used aspirin. | Unknown | Unknown | increased survival in cancers |
esophageal cancer | |||||
Macfarlane et al. [13] 2015 | Unknown | Unknown | Unknown | Unknown | improved survival was observed |
Spence et al. [11] 2018 | I 34 (1.6%) 10 (1.8%) II 69 (3.2%) 28 (5.0%) III 183 (8.4%) 47 (8.4%) IV 132 (6.1%) 23 (4.1%) Unknown 1756 (80.8%) 451 (80.7%) | Low-dose aspirin (75 mg) use | 182, 365, 548 and 730 tablets | Unknown | not associated with increased survival in sophageal or gastric cancer |
Spence et al. [11] 2018 | Unknown | Low-dose aspirin (75 mg) use | 182, 365, 548 and 730 tablets | Unknown | not associated with increased survival in sophageal or gastric cancer |
Frouws et al. [7] 2017 | Unknown | Nonusers were defined as patients who received for less than 30 days or never used aspirin. | Unknown | Unknown | increased survival in cancers |
Colorectal cancer | |||||
Chan et al. [17] 2009 | I 228 (32%) 193 (35%) II 260 (36%) 186 (33%) III 231 (32%) 181 (32%) I 218 (30%) 203 (37%) II265 (36%) 181 (33%) III 247 (34%) 165 (30%) | used aspirin 2 or more timesper week | Unknown | Headache, arthritis and other musculoskeletal pain, cardiovascular disease | associated with lower risk of colorectal cancer–specific and overall mortality |
Liao et all [20]. 2012 | I 112 (24%) 102 (30%) II 159 (34%) 87 (26%) III 128 (27%) 99 (29%) IV 31 (7%) 18 (5%) Unknown 36 (8%) 31 (9%) I 19 (20%) 27 (41%) II 36 (38%) 19 (29%) III 23 (24%) 14 (21%) IV 12 (13%) 3 (5%) Unknown 5 (5%) 3 (5%) | as regular use of aspirin duringmost weeks | Unknown | Headache, arthritis and other musculoskeletal pain, cardiovascular disease | associated with longer survival among patients with mutated-PIK3CA colorectal cancer |
Walker et al. [20] 2012 | Unknown | a repeat prescription (> 2) within the period | a fixed period of 1 year post-diagnosis | Unknown | have a potential as anti-neoplastics in diagnosed colorectal cancer |
Domingo et al. [18] 2013 | II 332 (48.7%) 57 (51.4%) III 349 (51.2%) (54 48.6%) II 46 (51.1%) 8 (57.1%) III 44 (48.9%) 6 (42.9%) | taking regularlow-dose aspirin at random assignment or who started during follow-up | Unknown | adjuvant setting of colorectal cancer: | support the prospective evaluation of adjuvant low-dose aspirin in patients with tumor PIK3CA mutation |
McCowan et al. [19] 2013 | Unknown | 28 tablets at one per day gave coverage for that prescription of 28 days. | date of the first prescription post-diagnosis to the end of coverage of the last prescription | Unknown | use post-diagnosis of colorectal cancer may reduce both all cause and colorectal cancer specific mortality |
Kothari et al. [21] 2015 | I 6(4%) 2(4%) II 50(37%) 16(33%) III 45(33%) 22(45%) IV 35(26%) 9(18%) | at least 75 mg of aspirin daily at the time of CRC diagnosis | Unknown | Unknown | significant improvements in survival in PIK3CA-mutated CRC patients |
Reimers et al. [5] 2014 | I 95 (13.8%) 38(21.2%) II 218 (31.9%) 69(38.5%) III 219 (32.0%) 57(31.8%) IV149(21.8%) 15(0.8%) Unknown 3 (0.4%) | given a prescription for aspirin for 14 days or more after a colon cancerdiagnosis | Unknown | Unknown | Increased PTGS2 expression or the presence of mutated PIK3CA did not predict benefit from aspirin |
Cardwell et al. [16] 2014 | I 65 (4.2%) II 283 (18.2%) III 565 (36.2%) IV 187 (12.0%) Missing 459 (29.4%) | low dose if 75 mg(0.3% of prescriptions after cancer diagnosis were 25 mg,98.5% were 75 mg, and 1.2% were 300 mg). | Duration of use was determined from quantity of tablets. | Unknown | low-dose aspirin usage after diagnosis of colorectal cancer did not increase survival time. |
Bains et al. [6] 2016 | I 3600 (21.9%) 1631 (27.7%) II 4840 (29.4%) 2112 (35.9%) III 4829 (29.3%) 1581 (26.8%) IV 3188 (19.4%) 565 (9.6%) | three or more prescriptions of aspirin starting from 30 days after the diagnosis of CRC | Aspirin prescriptions lasted 3 months at a time (100-tablet packets, one tablet once per day), | Unknown | Aspirin use after the diagnosis of CRC is independently associated with improved CSS and OS. |
Frouws et al. [7] 2017 | Unknown | Nonusers were defined as patients who received for less than 30 days or never used aspirin. | Unknown | Unknown | increased survival in cancers |
Newcomb et al. [14] 2017 | I 326 (30%) 311 (36%) II 391 (36%) 259 (30%) III 263 (24%) 225 (26%) IV 106 (10%) 61 7 (%) Unknown 311,166 | using the medications at least twice per week for more than 1 month | Pre-diagnostic use 1 year before diagnosis /post-diagnostic use between baseline and the 5-year follow-up interview | Unknown | regular use of NSAIDs after CRC diagnosis was significantly associated with improved survival in individuals with KRAS wild-type tumors |
Gray et al. [23] 2018 | A 1683(27.0%) 597(27.8%) B 2340(37.5%) 851(39.6%) C 2218(35.5%) 702(32.7%) | Low-dose (75 mg) aspirin exposure was identified from dispensing records within this database | users after a lag of 6 months after their first aspirin prescription | Unknown | either before or after diagnosis, did not prolong survival in this population-based CRC cohort. |
Joseph et al. [24] 2019 | Unknown | no less than 80 mg per day | at least a month | Unknown | lowers risk of both CRC-related mortality and overall mortality |
Zell et al. [15] 2009 | Unknown | taken aspirin regularly at least once a week | the total duration of use in number of years (< 1, 1, 2, 3–4, 5–9, or 10). | Unknown | NSAIDs are associated with decreased mortality among female CRC patients |
Din et al. [4] 2010 | Unknown | reported intake of aspirin | Unknown | Unknown | NSAID use prior to CRC diagnosis does not influence survival of colorectal cancer |
Coghill et al. [14] 2011 | Unknown | at least twice per week for 1 month | first, 0–6 months; second, 6 monthse2.5 years; third, 2.5–7 years; fourth, > 7 years). | Unknown | regular use of NSAIDs prior to diagnosis is associated with improved colorectal cancer survival |