The Role of Frailty and Myosteatosis in Predicting All-Cause Mortality in Older Adults with Cancer
2024

Frailty and Myosteatosis in Older Adults with Cancer

Sample size: 115 publication 10 minutes Evidence: moderate

Author Information

Author(s): Papadopoulos Efthymios, Wong Andy Kin On, Law Sharon Hiu Ching, Costa Sarah, Cheung Angela M., Rozenberg Dmitry, Alibhai Shabbir M. H.

Primary Institution: University Health Network, Toronto, Canada

Hypothesis

Does myosteatosis improve the predictive ability of frailty for all-cause mortality in older adults undergoing chemotherapy?

Conclusion

Myosteatosis improves the performance of frailty for predicting all-cause mortality in older adults with cancer.

Supporting Evidence

  • Frailty was a significant predictor of all-cause mortality with an adjusted hazard ratio of 1.68.
  • Myosteatosis was associated with a two-fold risk of all-cause mortality.
  • The combination of frailty and myosteatosis improved predictive performance for mortality.
  • 81.4% of frail participants had myosteatosis.
  • Median survival time was significantly different between frail and non-frail participants.

Takeaway

This study found that older adults with cancer who have both frailty and myosteatosis are at a higher risk of dying, and myosteatosis helps predict this risk better.

Methodology

A retrospective cohort study assessing frailty and myosteatosis in older adults (≥65 years) undergoing chemotherapy, using a frailty index and CT scans.

Potential Biases

Potential biases due to the retrospective design and lack of physical activity data.

Limitations

The study's retrospective nature limits causation inference, and the sample size may affect the generalizability of the results.

Participant Demographics

Mean age of participants was 77.1 years, with 71.3% male.

Statistical Information

P-Value

0.037 for frailty, 0.032 for myosteatosis

Confidence Interval

95% CI = 1.03–2.72 for frailty, 95% CI = 1.07–4.30 for myosteatosis

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.3390/curroncol31120578

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