Megestrol acetate 320 mg/day improved nutritional indices and reduced fatigue in cancer cachexia patients compared to diet alone.
This prospective quasi-experimental study enrolled 97 patients with cancer cachexia. The intervention group received regular diet plus megestrol acetate (MA) 320 mg/day, while the comparator group received regular diet alone. The follow-up period was 2 months. No reported drug-related adverse events or discontinuations were observed, indicating the regimen was well-tolerated in this cohort.
Regarding primary outcomes, the MA group demonstrated significant improvements in body weight, BMI, fat mass, prealbumin, albumin, and hemoglobin compared to baseline. These improvements were significantly greater in the MA group compared to the control group. Skeletal muscle mass was maintained in the MA group, whereas the control group experienced significant loss, resulting in a significant between-group difference.
For secondary outcomes, the MA group showed significant reduction in IL-6 levels compared to baseline and markedly greater reductions compared to the control group. Cancer-related fatigue across all domains decreased significantly in the MA group compared to baseline, with reductions markedly greater than in the control group. Quality of life showed more substantial improvement in the MA group compared to the control group. Conversely, most inflammatory or immune markers, including CD4+ and CD8+ T cells, showed no significant between-group differences.
The study design is a prospective quasi-experimental study, which precludes definitive causal conclusions. As the study phase, publication type, setting, and funding sources were not reported, the generalizability of these findings remains uncertain. Clinicians should interpret these results with caution regarding the specific efficacy of MA for cancer cachexia.