2021
DOI: 10.1002/cncr.33956
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Self‐reported quality of life as a predictor of mortality in renal cell carcinoma

Abstract: BACKGROUND:This study evaluated the utility of self-reported quality of life (QOL) metrics in predicting mortality among all-comers with renal cell carcinoma (RCC) and externally tested the findings in a registry of patients with small renal masses. METHODS: The Surveillance, Epidemiology, and End Results-Medicare Health Outcomes Survey (SEER-MHOS) captured QOL metrics composed of mental component summary (MCS) and physical component summary (PCS) scores. Regression models assessed associations of MCS and PCS … Show more

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Cited by 8 publications
(3 citation statements)
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“…A change in PCS or MCS scores of 1 to 2 points or greater has been shown to be predictive of other important health outcomes. For instance, each additional PCS and MCS point decreased the risk of death from any cause by 2.3% and 1.3%, respectively, in patients with renal cell carcinoma (Alam et al, 2022).…”
Section: Applications Of the Vr-12mentioning
confidence: 99%
“…A change in PCS or MCS scores of 1 to 2 points or greater has been shown to be predictive of other important health outcomes. For instance, each additional PCS and MCS point decreased the risk of death from any cause by 2.3% and 1.3%, respectively, in patients with renal cell carcinoma (Alam et al, 2022).…”
Section: Applications Of the Vr-12mentioning
confidence: 99%
“…Additionally, patients who have lower QOL may report more negative clinical and psychological outcomes. Specifically, lower QOL related-indicators were associated with a higher risk of all-cause mortality and unplanned readmission ( 8 , 9 ). Conversely, those outcomes were negatively associated with QOL, creating a vicious cycle that ultimately may lead to a decreased life expectancy ( 10 ).…”
Section: Introductionmentioning
confidence: 99%
“…Although many individual national surveys by patient organisations [4,5] have been conducted over the years, they either focused on one particular aspect of psychological wellbeing (eg, distress or fear of recurrence) or were not peer-reviewed and published in the literature, and no conclusions could be drawn about country-level variations in patient experience or best practice. Other examples of patient-reported surveys in the literature include those that measure physical health and quality of life [6] but these did not prioritise the unmet needs of this group across the care pathway. Here we report on the first global patient survey on the diagnosis, management, and burden of RCC conducted by the International Kidney Coalition (IKCC) and involving its affiliate organisations worldwide.…”
mentioning
confidence: 99%