Abstract 1822P
Background
The incidence and economic burden of cancer cachexia are not well described. Study objective: estimate cachexia incidence and compare HRU in patients with solid tumors with and without cachexia.
Methods
This retrospective study was conducted using the Optum Market Clarity database. Patients had breast, colorectal, lung, pancreatic, or prostate cancer between 10/1/2016-9/30/2022 and ≥2 weight measurements 150-210 days apart with ≥1 measurement after cancer index date. Cachexia cases had ≥5% weight loss between measurements (Fearon criteria); date of second measurement was designated the cachexia index date. Controls had <5% weight loss; index dates imputed as the second of 2 weight measurements 150-210 days apart. Inverse probability of treatment weights were used to balance both groups at cachexia index date. Primary outcome: number of healthcare visits/patient/month (PPPM) during the 12 months after cachexia index date, categorized as hospital inpatient (IP) admissions, hospital outpatient (OP), office, home/telehealth, and other visits. T-tests were used to compare HRU in cachexia cases vs controls by tumor type.
Results
27679 patients with breast (N=9660), colorectal (N=3080), lung (N=3116), pancreatic (N=449), or prostate (N=8650) cancer were included. 12 months after cancer diagnosis, 34%, 51%, 55%, 73%, and 29% of patients, respectively, had cachexia. Across tumor types, significantly more hospital OP visits PPPM occurred in cachexia vs controls (Table). Differences in hospital IP, office, home/telehealth, and other visits were observed, with statistical significance varying by tumor type. Table: 1822P
PPPM claims by tumor type in cachexia cases vs controls
Breast | Colorectal | Lung | Pancreatic | Prostate | |||||||||||
Cachexia Cases (n=3289) | Controls (n=6371) | p | Cachexia Cases (n=1576) | Controls (n=1504) | p | Cachexia Cases (n=1725) | Controls (n=1391) | p | Cachexia Cases (n=326) | Controls (n=123) | p | Cachexia Cases (n=2536) | Controls (n=6114) | p | |
Hospital IP | 0.57 | 0.49 | .197 | 1.71 | 1.42 | .190 | 4.10 | 3.48 | .164 | 5.10 | 7.01 | .236 | 0.90 | 0.41 | ConclusionsIncidence of cachexia was highest in pancreatic followed by lung and colorectal, and lowest in breast and prostate cancers. Patients with cachexia used more health resources than controls, collectively highlighting clinical and economic burden in this population. Clinical trial identificationEditorial acknowledgementLegal entity responsible for the studyPfizer. FundingPfizer. DisclosureI. Ali: Financial Interests, Personal, Full or part-time Employment: Icahn School of Medicine at Mount Sinai. S. Dagenais,I. Jacobs, F. Dai, O. Dina: Financial Interests, Personal, Full or part-time Employment: Pfizer; Financial Interests, Personal, Stocks/Shares: Pfizer. S. Corman, T. Adesoba: Financial Interests, Personal, Full or part-time Employment: PRECISIONheor; Financial Interests, Institutional, Other, Consulting fees to PRECISIONheor: Pfizer. Resources from the same session1843P - Safety of immunotherapy in cancer patients with comorbidities: Results of the phase IV Italian immuno-special trialPresenter: Davide Smussi Session: Poster session 12 1844P - 3-year experience of the Belgian multidisciplinary immunotoxicity board (BITOX): A nationwide initiative of the Belgian Society of Medical Oncology (BSMO)Presenter: Marthe Verhaert Session: Poster session 12 1845P - The impact of body mass index (BMI) on immune-related adverse events (irAEs) and acute care use among patients receiving immune checkpoint inhibitors (ICIs): A population-based studyPresenter: Zac Coyne Session: Poster session 12 1846P - Social determinants of health in studies assessing toxicities associated with immune checkpoint inhibitor treatment: A systematic reviewPresenter: Sofia Georgopoulou Session: Poster session 12 1847P - Safety and efficacy of immune checkpoint inhibitors in patients over 85 years: ICIPO85 studyPresenter: MYRTILLE THOMAS Session: Poster session 12 1848P - Safety and efficacy of immune checkpoint inhibitors in patients with cancer and hepatitis B: Multicentre experiencePresenter: Onur Bas Session: Poster session 12 1849P - Clinical predictors of long-term responses to immune checkpoint inhibitors (ICI) in a multi-tumor cohortPresenter: Víctor Albarrán Fernández Session: Poster session 12 1850P - Management and potential factors of immunotoxicity in patients with metastatic non-small cell lung cancer receiving first-line treatment with immune checkpoint inhibitorsPresenter: Jesús Peña-Lopez Session: Poster session 12 1851P - Prognostic impact of myosteatosis on survival with immune checkpoint inhibitors: A systematic review and meta-analysisPresenter: Taha Koray Sahin Session: Poster session 12 1852P - The use of patient-reported outcome measures to assess toxicities and quality of life associated with immune checkpoint inhibitor therapy: A systematic reviewPresenter: Poorni Jaganathan Session: Poster session 12 This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used. For more detailed information on the cookies we use, please check our Privacy Policy.
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