Epidemiology and survival outcomes for liposarcoma patients in England: An observational cohort study using real world data

<b>Purpose:</b> This real-world data study evaluates demographic and clinical characteristics and survival in patients with liposarcoma to inform our understanding of treatment patterns and associated outcomes in this rare cancer. <b>Materials and methods:</b> A retrospective cohort study was conducted using existing data available through the Clinical Practice Research Datalink. Male and female patients aged 18 years or older who had their first ever record of liposarcoma between 1998 and 2018 were included in the study. The demographic and tumour characteristics were presented (overall, by first line treatment and for dedifferentiated liposarcoma only) as proportions (percentages) while continuous variables were presented as means with standard deviation and interquartile ranges. Survival rates from diagnosis date and first line treatment (with 95% confidence intervals) were also calculated. <b>Results:</b> 1,315 patients were included, of which 46% (611) had a treatment recorded. Most patients were male and over the age of 60 years. Surgery was the most frequent treatment received following diagnosis (34% of all patients), followed by radiotherapy (8%) and chemotherapy (2.4%) with the remaining patients having no record of treatment available. Overall, there was a 77% probability of survival after diagnosis at 5 years. <b>Conclusions:</b> Findings from this study help advance our understanding of real world patient characteristics, treatment patterns and survival outcomes in a rare and heterogeneous cancer, which may be useful for guiding clinical management. This study also identified challenges with using real world data, which can be minimised through improving data collection and standardisation.

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Publication Details

Journal
Rare Tumors
Published
2025-07-26
DOI
https://doi.org/10.1177/20363613251346621
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
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article

Epidemiology and survival outcomes for liposarcoma patients in England: An observational cohort study using real world data

Monika Frysz, Rachael Williams, Eleanor Yelland, Robin L. Jones et al.
Rare Tumors
Sarcoma Diagnosis and Treatment
article

Epidemiology and survival outcomes for liposarcoma patients in England: An observational cohort study using real world data

Monika Frysz, Rachael Williams, Eleanor Yelland, Robin L. Jones, Jessie O. Oyinlola, Amy Walker, Mounia Beloueche-Babari
article en

Abstract

<b>Purpose:</b> This real-world data study evaluates demographic and clinical characteristics and survival in patients with liposarcoma to inform our understanding of treatment patterns and associated outcomes in this rare cancer. <b>Materials and methods:</b> A retrospective cohort study was conducted using existing data available through the Clinical Practice Research Datalink. Male and female patients aged 18 years or older who had their first ever record of liposarcoma between 1998 and 2018 were included in the study. The demographic and tumour characteristics were presented (overall, by first line treatment and for dedifferentiated liposarcoma only) as proportions (percentages) while continuous variables were presented as means with standard deviation and interquartile ranges. Survival rates from diagnosis date and first line treatment (with 95% confidence intervals) were also calculated. <b>Results:</b> 1,315 patients were included, of which 46% (611) had a treatment recorded. Most patients were male and over the age of 60 years. Surgery was the most frequent treatment received following diagnosis (34% of all patients), followed by radiotherapy (8%) and chemotherapy (2.4%) with the remaining patients having no record of treatment available. Overall, there was a 77% probability of survival after diagnosis at 5 years. <b>Conclusions:</b> Findings from this study help advance our understanding of real world patient characteristics, treatment patterns and survival outcomes in a rare and heterogeneous cancer, which may be useful for guiding clinical management. This study also identified challenges with using real world data, which can be minimised through improving data collection and standardisation.

Rare TumorsVol. 17
Institute of Cancer Research (GB), Royal Ottawa Mental Health Centre (CA), Clinical Practice Research Datalink (GB), Boehringer Ingelheim (United Kingdom) (GB), Royal Marsden Hospital (GB), Boehringer Ingelheim (Egypt) (EG)
Good health and well-being
Openalex Percentile: Top 71%
Sarcoma Diagnosis and Treatment
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