High-dose dexamethasone fails to improve dyspnea in cancer patients: Lancet

Written By :  Jacinthlyn Sylvia
Medically Reviewed By :  Dr. Kamal Kant Kohli
Published On 2022-09-18 14:30 GMT   |   Update On 2022-09-18 14:31 GMT

USA: A new study published in The Lancet Oncology showed that high-dose dexamethasone was linked to increased adverse events and did not significantly improve dyspnea in cancer patients.Despite the lack of evidence supporting their effectiveness, systemic corticosteroids are frequently recommended to cancer patients to relieve their dyspnea. In order to compare the impact of...

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USA: A new study published in The Lancet Oncology showed that high-dose dexamethasone was linked to increased adverse events and did not significantly improve dyspnea in cancer patients.

Despite the lack of evidence supporting their effectiveness, systemic corticosteroids are frequently recommended to cancer patients to relieve their dyspnea. In order to compare the impact of high-dose dexamethasone to placebo on cancer-related dyspnea, David Hui and colleagues carried out this study.

The University of Texas MD Anderson Cancer Center and the general oncology clinic at Lyndon B. Johnson General Hospital both participated in the randomized, controlled experiment. Dexamethasone 8 mg orally every 12 hours for 7 days, followed by 4 mg orally every 12 hours for 7 days, or identical placebo capsules for 14 days were randomly assigned (2:1) to ambulatory cancer patients, with an average or higher dyspnea intensity score on an 11-point numerical rating scale. To determine group assignments, patients, researchers, and doctors were concealed. The main result was the change in dyspnea NRS intensity from baseline to day 7 (around two days) throughout the previous 24 hours. 

The key findings of this study were:

1. 2867 people were examined between January 11, 2018, and April 23, 2021, 128 participants were recruited and randomly allocated to receive dexamethasone (n = 85) or a placebo (n = 43).

2. There was no statistically significant between-group difference in the mean change in dyspnea NRS intensity from baseline to day 7 (2 days), which was -16 in the dexamethasone group and -16 in the placebo group.

3. Infections, sleeplessness, and neuropsychiatric symptoms were the most frequent all-cause grade 3–4 adverse events.

4. Three (7%) of the 43 patients in the placebo group and 24 (28%) of the 85 patients who received dexamethasone reported experiencing serious side effects, all of which required hospital hospitalization.

'High-dose dexamethasone shouldn't be regularly administered to cancer patients to treat dyspnea due to the dangers involved. This research does not rule out the possibility that some advantages might accrue to a subpopulation of patients, though. To optimize the risk-benefit ratio, more research on corticosteroids for symptom management is required to find the proper dose in the appropriate individuals," said the PI in conclusion. 

Reference: 

Hui, D., Puac, V., Shelal, Z., Dev, R., Hanneman, S. K., Jennings, K., Ma, H., Urbauer, D. L., Shete, S., Fossella, F., Liao, Z., Blumenschein, G., Gandhi, S. J., Tsao, A., Mahler, D. A., & Bruera, E. (2022). Effect of dexamethasone on dyspnoea in patients with cancer (ABCD): a parallel-group, double-blind, randomised, controlled trial. In The Lancet Oncology. Elsevier BV. https://doi.org/10.1016/s1470-2045(22)00508-3

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Article Source : The Lancet Oncology

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