Dose‐dependent effect of megestrol acetate supplementation in cancer patients with anorexia–cachexia syndrome: A meta‐analysis

Author:

Talebi Sepide12,Zeraattalab‐Motlagh Sheida3,Barkhordar Maryam45,Vaezi Mohammad65,Ghoreishy Seyed Mojtaba78,Ghavami Abed9,Hosseini Yasaman2,Travica Nikolaj10,Mohammadi Hamed25

Affiliation:

1. Students' Scientific Research Center (SSRC) Tehran University of Medical Sciences Tehran Iran

2. Department of Clinical Nutrition, School of Nutritional Sciences and Dietetics Tehran University of Medical Sciences Tehran Iran

3. Department of Health and Human Performance University of Houston Houston TX USA

4. Cell Therapy and Hematopoietic Stem Cell Transplantation Research Center Tehran University of Medical Sciences Tehran Iran

5. Research Institute for Oncology, Hematology and Cell Therapy Tehran University of Medical Sciences Tehran Iran

6. Hematology, Oncology and Stem Cell Transplantation Research Center Tehran University of Medical Sciences Tehran Iran

7. Department of Nutrition, School of Public Health Iran University of Medical Sciences Tehran Iran

8. Student Research Committee, School of Public Health Iran University of Medical Sciences Tehran Iran

9. Department of Clinical Nutrition, School of Nutrition and Food Science Isfahan University of Medical Sciences Isfahan Iran

10. IMPACT—Institute for Mental and Physical Health and Clinical Translation, Food and Mood Centre, School of Medicine, Barwon Health Deakin University Geelong Australia

Abstract

AbstractThere is inconsistent evidence relating to the effects of megestrol acetate (MA) supplementation on cancer patients suffering from anorexia–cachexia syndrome. This review aimed to examine the dose–response effect of MA supplementation in patients with cancer‐associated anorexia/cachexia. Relevant keywords were searched in PubMed, Scopus and ISI Web of Science from inception to June 2023 for randomized controlled trials (RCTs) examining the effect of MA on pathologies in patients with cancer‐associated cachexia. Our primary outcomes were changes in body weight and appetite. However, fatigue and quality of life were secondary outcomes. The mean difference (MD) and 95% confidence interval (95% CI) were estimated using the random‐effects method. Thirteen trials comprising 1229 participants (mean age 60 years) were identified. The results of our highest versus lowest analysis revealed that MA supplementation was not associated with any increase in body weight (MD: 0.64 kg, 95% CI [−0.11, 1.38], P = 0.093, I2 = 69.1%; GRADE = very low certainty). Twelve trials, including 14 effect sizes derived from 1369 patients (intervention = 689, control = 680), provided data on the effect of MA on body weight. Subgroup analyses showed a significant increase in body weight following short‐term intervention (≤8 weeks) and a combination of radiation/chemotherapy as concurrent treatment. A linear dose–response meta‐analysis indicated that each 200 mg/day increment in MA consumption had a significant increase in weight gain (MD: 0.44; 95% CI [0.13, 0.74], P = 0.005; I2 = 97.1%); however, the magnitude of the effect was small. MA administration significantly affected the quality of life based on pooled effect sizes (MD: 1.15, 95% CI [0.76, 1.54], P < 0.001, I2 = 0%; n = 2 RCTs including 176 patients; GRADE = very low certainty). However, no significant effect of MA supplementation was observed on appetite (MD: 0.29, 95% CI [−0.05, 0.64], P = 0.096, I2 = 18.3%; n = 3 RCTs including 163 patients; GRADE = very low certainty) and fatigue (MD: 0.14, 95% CI [−0.09, 0.36], P = 0.236, I2 = 0%; n = 2 RCTs including 300 patients; GRADE = very low certainty). With very low certainty of the evidence, MA supplementation may not lead to a significantly increased weight gain and other outcomes.

Funder

Tehran University of Medical Sciences and Health Services

Publisher

Wiley

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