Copyright
©The Author(s) 2016.
World J Gastroenterol. Jul 21, 2016; 22(27): 6100-6113
Published online Jul 21, 2016. doi: 10.3748/wjg.v22.i27.6100
Published online Jul 21, 2016. doi: 10.3748/wjg.v22.i27.6100
Ref. | Year | Study design | Type of diabetes | Results |
Maynard[43] | 1910 | Case-control | Not differentiated | Cancer mortality increased |
Greenwood and Wood[44] | 1914 | Case-control | Not differentiated | Cancer mortality increased in American cities; no significant correlation was observed in European cities |
Marble[45] | 1934 | Case-control | Not differentiated | Pancreatic cancer incidence increased |
Kessler[46] | 1970 | Case-control | Not differentiated | Pancreatic cancer deaths increased |
Lawson et al[47] | 1986 | Case-control | Not differentiated | HCC incidence increased (HR = 3.9) |
Levine et al[67] | 1990 | Cohort | IGT | HCC deaths increased in men; post-load plasma glucose increased |
Adami et al[48] | 1991 | Cohort | Not differentiated | Incidences of primary liver (RR = 1.5), pancreatic (RR = 1.4) and endometrial (RR = 1.5) cancers increased |
Smith et al[164] | 1992 | Cohort | IGT | Pancreatic cancer increased (RR = 2.25); post-load plasma glucose increased in IGT men. HCC was not analyzed in organ-specific statistics |
La Vecchia et al[51] | 1994 | Case-control | Not differentiated | Liver cancer incidence remained elevated 10 yr after the diagnosis of diabetes (RR = 2.6) |
Adami et al[49] | 1996 | Cohort | Not differentiated | Primary liver cancer incidence increased (SIR = 4.7 in men and 3.4 in women) |
Wideroff et al[50] | 1997 | Cohort | Not differentiated | Primary liver cancer incidence increased (SIR = 4.0 in men and 2.1 in women) |
La Vecchia et al[165] | 1997 | Case-control | Not differentiated | Liver cancer incidence increased (OR = 2.2) for at least 10 yr after the diagnosis of diabetes |
Ikeda et al[54] | 1998 | Cohort | Not differentiated | Recurrence-free survival after hepatic resection decreased in diabetic cases |
Balkau et al[52] | 2001 | Cohort | Not differentiated | HCC incidence increased with fasting hyperinsulinemia (HR = 2.72) and 2-h hyperinsulinemia (HR = 3.41) |
Huo et al[55] | 2003 | Cohort | Not differentiated | HCC recurrence increased in HBV-seropositive cases |
Coughlin et al[58] | 2004 | Cohort | Not differentiated | Liver cancer mortality increased in men (RR = 2.19) |
Batty et al[68] | 2004 | Cohort | IGT | HCC (HR = 2.47) and pancreatic cancer (HR = 1.35) increased; post-load plasma glucose increased in IGT men |
El-Serag et al[60] | 2006 | Meta-analysis | Not differentiated | HCC incidence increased in 9 case-control studies (OR = 2.5) and 7 cohort studies (OR = 2.5) |
Inoue et al[64] | 2006 | Cohort | Not differentiated | HCC incidence increased (HR = 2.24 in men and 1.94 in women) |
Komura et al[56] | 2007 | Cohort | Not differentiated | Postoperative recurrence-free survival decreased in diabetic cases |
Kawamura et al[57] | 2008 | Cohort | Not differentiated | HCC recurrence increased (HR = 4.61) |
Landman et al[59] | 2010 | Cohort | Type 2 | HCC death increased (SMR = 1.47) |
Lee et al[53] | 2011 | Cohort | Type 2 | Incidences of total cancer, HCC and pancreatic cancer increased |
Hense et al[166] | 2011 | Cohort | Type 2 | HCC incidence increased (SIR = 1.94) |
Johnson et al[70] | 2011 | Cohort | Type 2 | After detection biases were excluded, incidences of HCC (HR = 2.53), pancreatic (HR = 1.65) and endometrial (HR = 1.58) cancers increased |
Wang et al[167] | 2012 | Meta-analysis | Type 1 and type 2 | HCC incidence (RR = 2.23) and mortality (RR = 2.43) increased in cohort studies |
Wang et al[168] | 2012 | Meta-analysis | Not differentiated | HCC incidence (RR = 2.01) and mortality (RR = 1.56) increased |
Lai et al[101] | 2012 | Cohort | Not differentiated | HCC incidence increased (HR = 1.73) |
Schlesinger et al[62] | 2013 | Cohort | Not differentiated | HCC incidence increased (RR = 2.17) in HBV/HCV-negative individuals |
Koh et al[63] | 2013 | Cohort | Not differentiated | HCC incidence increased (HR = 2.14), particularly in non-viral cases (HR = 5.15) |
Wang et al[169] | 2014 | Meta-analysis | Not differentiated | HCC in diabetic cases was related to overall survival (RR = 1.46) and disease-free survival (RR = 1.57) |
Harding et al[69] | 2015 | Case-control | Type 1 and type 2 | Incidences of total, liver, pancreatic and endometrial cancer increased in cases involving type 2 diabetes mellitus |
Ref. | Year | Study design | Type of diabetes | Results |
Evans et al[26] | 2005 | Case-control | Type 2 | HCC incidence decreased (OR = 0.79) |
Bowker et al[96] | 2006 | Cohort | Type 2 | Mortality was lower among metformin users than among insulin or sulfonylurea users (HR = 0.77) |
Libby et al[97] | 2009 | Cohort | Type 2 | Total cancer incidence decreased (HR = 0.63) |
Donadon et al[98] | 2009 | Case-control | Type 2 | HCC incidence was lower among metformin users (OR = 0.33) than among insulin users (OR = 2.99) |
Donadon et al[99] | 2010 | Cohort | Type 2 | HCC incidence was lower among metformin users (OR = 0.15) than among insulin or sulfonylurea users |
Hassan et al[100] | 2010 | Case-control | Not differentiated | HCC incidence decreased (OR = 0.30) |
Home et al[107] | 2010 | Randomized controlled trial | Type 2 | Total cancer incidence did not decrease compared with rosiglitazone users |
Landman et al[59] | 2010 | Cohort | Type 2 | HCC deaths decreased (HR = 0.43) |
Hosono et al[119] | 2010 | Randomized controlled trial | Non-diabetic | A surrogate marker of colorectal cancer incidence decreased |
Ferrara et al[104] | 2011 | Cohort | Not differentiated | No decreases in the incidence of any cancer; no data on HCC were available |
Lee et al[53] | 2011 | Cohort | Type 2 | Incidences of total cancer (HR = 0.12), HCC (HR = 0.06) and colorectal cancer (HR = 0.36) decreased |
Hense et al[166] | 2011 | Cohort | Type 2 | HCC incidence did not decrease |
Lai et al[101] | 2012 | Cohort | Not differentiated | HCC incidence was decreased by metformin (HR = 0.49) and thiazolidinedione (HR = 0.56) |
Ruiter et al[170] | 2012 | Cohort | Not differentiated | Incidences of total cancer (HR = 0.90) and HCC (HR = 0.67) were lower among metformin users than among sulfonylurea users |
Stevens et al[108] | 2012 | Meta-analysis | Type 2 and at-risk for diabetes | The summary RR for cancer outcomes was 1.02 across all trials |
Thakkar et al[109] | 2013 | Meta-analysis | Type 2 | Total cancer incidence decreased in case-control studies (RR = 0.90) and cohort studies (RR = 0.70) but did not significantly decrease in randomized controlled trials |
Yin et al[110] | 2013 | Meta-analysis | Type 2 | Overall survival (HR = 0.65) and cancer-specific survival (HR = 0.62) for total cancers were better for metformin than for other glucose-lowering medications |
Tsilidis et al[105] | 2014 | Cohort | Type 2 | Incidences of total cancer and HCC were not significantly lower among metformin users than among sulfonylurea users |
Gandini et al[106] | 2014 | Meta-analysis | Not differentiated | After adjusting for time-related biases, total cancer incidence decreased (RR = 0.90), but this decrease became insignificant after adjusting for BMI in addition to time-related biases. Total cancer mortality and HCC incidence did not decrease after adjusting for time-related biases |
Higurashi et al[120] | 2016 | Randomized controlled trial | Non-diabetic | Incidences of metachronous colorectal adenomas (HR = 0.60) and total polyps (HR = 0.67) decreased |
- Citation: Fujita K, Iwama H, Miyoshi H, Tani J, Oura K, Tadokoro T, Sakamoto T, Nomura T, Morishita A, Yoneyama H, Masaki T. Diabetes mellitus and metformin in hepatocellular carcinoma. World J Gastroenterol 2016; 22(27): 6100-6113
- URL: https://www.wjgnet.com/1007-9327/full/v22/i27/6100.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i27.6100