Background: mTOR inhibitors are now approved by regulatory agencies for the treatment of a variety of malignancies. The risk of metabolic complications with these agents is not well characterized. Methods: PubMed was searched for articles published from 2001 until 2011. Eligible studies included prospective randomized trials evaluating temsirolimus, everolimus, and ridaforolimus in patients with all solid tumor malignancies. Sixteen eligible phase II clinical trials and 8 randomized controlled clinical trials were included in a systematic review and meta-analysis and the number of metabolic related AEs (hyperglycemia, hypercholesterolemia, and hypertriglyceridemia) was extracted. Incidence rates and incident rate ratios were calculated. Findings: Twenty-four trials, including 4261 patients, were included in the calculation of the incidence rate. The average incidence rate of all grade metabolic related events was 0.70 (95% CI, 0.47, 0.93). The average incidence rate of serious (grade 3 and 4) metabolic related adverse events was 0.11 (95% CI, 0.08, 0.15). The incidence rate ratio (IRR) of a metabolic adverse event with mTOR inhibitor therapy compared with control was 2.93 (95% CI, 2.33, 3.70) and of serious grade 3 and 4 metabolic adverse events was 4.58 (95% CI, 2.86, 7.34). The IRR of all grade hyperglycemia was 2.95 (95% CI, 2.14, 4.05) and of grade 3-4 hyperglycemia was 5.25 (95% CI, 3.07, 9.00). The IRR of all grade hypertriglyceridemia was 2.49 (95% CI, 1.76, 3.52) and of grade 3-4 hypertriglyceridemia was 2.01 (95% CI, 0.65, 6.27). The IRR of all grade hypercholesterolemia was 3.35 (95% CI, 2.17, 5.18) and of grade 3-4 hypercholesterolemia was 6.51 (95% CI, 1.48, 28.59). These findings suggest a statistically significant increase in the risk of hyperglycemia, hypercholesterolemia (all grades and grade 3 and 4), and all grade hypertriglyceridemia associated with mTOR therapy when compared with control. Interpretation: The risk of all grade and grade 3-4, hyperglycemia, hypercholesterolemia, and hypertriglyceridemia, are increase in patients treated with mTOR inhibitors compared with control. (C) 2013 Elsevier Ltd. All rights reserved.
机构:
Great North Childrens Hosp, Dept Paediat Nephrol, Newcastle Upon Tyne, England
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Newcastle Upon Tyne Hosp NHS Fdn Trust, Paediat Immunol & Infect Dis, Newcastle Upon Tyne, Turkiye
Newcastle Univ, Populat Hlth Sci Inst, Newcastle Upon Tyne, TurkiyeGreat North Childrens Hosp, Dept Paediat Nephrol, Newcastle Upon Tyne, England
Owens, Stephen
Sayer, John
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Newcastle Univ, Inst Genet Med, Newcastle Upon Tyne, England
NIHR Newcastle Biomed Res Ctr, Newcastle Upon Tyne, TurkiyeGreat North Childrens Hosp, Dept Paediat Nephrol, Newcastle Upon Tyne, England
Sayer, John
ARCHIVES OF DISEASE IN CHILDHOOD-EDUCATION AND PRACTICE EDITION,
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Sungkyunkwan Univ, Sch Med, Div Hematol Oncol, Dept Med,Samsung Med Ctr, Seoul 06351, South Korea
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Sungkyunkwan Univ, Sch Med, Dept Urol, Samsung Med Ctr, Seoul 06351, South KoreaSungkyunkwan Univ, Sch Med, Div Hematol Oncol, Dept Med,Samsung Med Ctr, Seoul 06351, South Korea
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Sungkyunkwan Univ, Sch Med, Dept Urol, Samsung Med Ctr, Seoul 06351, South KoreaSungkyunkwan Univ, Sch Med, Div Hematol Oncol, Dept Med,Samsung Med Ctr, Seoul 06351, South Korea
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Sungkyunkwan Univ, Sch Med, Div Hematol Oncol, Dept Med,Samsung Med Ctr, Seoul 06351, South KoreaSungkyunkwan Univ, Sch Med, Div Hematol Oncol, Dept Med,Samsung Med Ctr, Seoul 06351, South Korea
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Guangdong Med Univ, Guangdong Key Lab Res & Dev Nat Drugs, Zhanjiang, Peoples R China
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Guangdong Med Univ, Guangdong Key Lab Res & Dev Nat Drugs, Zhanjiang, Peoples R China
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Univ Calif Los Angeles, Dept Med, Div Infect Dis, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Med, Div Infect Dis, Los Angeles, CA 90095 USA