Metabolic complications with the use of mTOR inhibitors for cancer therapy

被引:61
|
作者
Sivendran, Shanthi [1 ]
Agarwal, Neeraj [2 ,3 ]
Gartrell, Benjamin [4 ]
Ying, Jian [3 ]
Boucher, Kenneth M. [3 ]
Choueiri, Toni K. [5 ]
Sonpavde, Guru [6 ]
Oh, William K. [7 ]
Galsky, Matthew D. [7 ]
机构
[1] Lancaster Gen Hlth, Lancaster, PA USA
[2] Univ Utah, Sch Med, Div Hematol Oncol, Salt Lake City, UT 84112 USA
[3] Huntsman Canc Inst, Salt Lake City, UT USA
[4] Albert Einstein Coll Med, Montefiore Med Ctr, Dept Med Oncol, Bronx, NY 10467 USA
[5] Dana Farber Canc Inst, Boston, MA USA
[6] Univ Alabama Birmingham, Birmingham Comprehens Canc Ctr, Birmingham, AL USA
[7] Mt Sinai Sch Med, Tisch Canc Inst, Div Hematol Oncol, New York, NY USA
关键词
Cancer; mTOR inhibitor; Metabolic; Temsirolimus; Everolimus; Ridaforolimus; Adverse events; PHASE-II TRIAL; MAMMALIAN TARGET; TEMSIROLIMUS CCI-779; RAPAMYCIN INHIBITOR; CELL CARCINOMA; DOSE LEVELS; EVEROLIMUS; RAD001;
D O I
10.1016/j.ctrv.2013.04.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:190 / 196
页数:7
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