Abstract
Patients with cancer are often treated with glucocorticoids (gcs) as part of therapy, which may cause hyperglycemia. We sought to define the prevalence of, and risk factors for, hyperglycemia in this setting. Adult patients taking gc as part of therapy protocols for primary brain tumour or metastasis, for lymphoma, or for bone marrow transplant (bmt) were screened with random glucometer measurements taken at least 3 hours after the last dose gcs. We screened 90 patients [44.4% women, 55.6% men; mean age: 59.6 years (range: 25-82 years); mean body mass index (bmi): 26.4 kg/m(2) (range: 15.8-45.3 kg/m(2))] receiving gc as part of cancer treatment. Mean total daily gc dose in the group was 238.5 mg (range: 30-1067 mg) hydrocortisone equivalents. Hyperglycemia (glucose ≥ 8.0 mmol/L) was found in 58.9% (53 of 90), and diabetes mellitus (dm)-range hyperglycemia (glucose ≥ 11.1 mmol/L) in 18.9% (17 of 90). The mean time from gc ingestion to glucometer testing was 5.5 hours (range: 3-20 hours). Presence of hyperglycemia did not correlate with traditional dm risk factors such as age, sex, bmi, and personal or family history of dm. A longer interval from gc dose to testing (p < 0.05), a higher gc dose (p = 0.04), and a shorter interval between the preceding meal and testing (p = 0.02) were risk factors for hyperglycemia in some patient groups. Glucocorticoid-induced hyperglycemia is common in patients undergoing cancer treatment and cannot be predicted by traditional risk factors for dm. We recommend that all cancer patients receiving gc be screened for hyperglycemia at least 4-6 hours after gc administration.
Highlights
Hyperglycemia is emerging as a potential risk factor for the development of cancer, and it may be associated with poor cancer treatment outcomes
Presence of hyperglycemia did not correlate with traditional dm risk factors such as age, sex, bmi, and personal or family history of dm
Glucocorticoid-induced hyperglycemia is common in patients undergoing cancer treatment and cannot be predicted by traditional risk factors for dm
Summary
Hyperglycemia is emerging as a potential risk factor for the development of cancer, and it may be associated with poor cancer treatment outcomes. In a cohort of 278 adults undergoing induction therapy for acute lymphocytic leukemia (all) combined with glucocorticoid (gc) therapy, Weiser et al 13 reported diabetes-range hyperglycemia (≥11.1 mmol/L 14) in 37% of the patients—a condition that was associated with a lesser duration of complete all remission, decreased overall survival, and increased rates of infection and sepsis 15 Another retrospective cohort study of 283 hospitalized patients with acute myeloid leukemia demonstrated increased rates of hospital mortality and sepsis associated with blood glucose levels of 6.1 mmol/L or more 16, and a study of patients with newly diagnosed glioblastoma reported a significantly lesser overall survival duration in the presence of blood glucose levels greater than 7.6 mmol/L regardless of gc dose 17. We sought to define the prevalence of, and risk factors for, hyperglycemia in this setting
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