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 session1874P - Time to vomiting after chemotherapy in association with number of emetic risk factors among breast cancer patients receiving highly emetogenic chemotherapyPresenter: Winnie Yeo Session: Poster session 12 1875P - Real-world evidence of ribociclib induced liver toxicity in patients with breast cancer: A multi-center experiencePresenter: Onur Bas Session: Poster session 12 1877P - Adverse effects (AEs) of trastuzumab deruxtecan (T-DXd) in solid tumours: A meta-analysisPresenter: Neha Pathak Session: Poster session 12 1878P - Efficacy of surgical gloves (SG) as compression therapy to prevent oxaliplatin-induced peripheral neuropathy (PN): The ELEGANT trialPresenter: Aurélia JOUREAU-CHABERT Session: Poster session 12 1879P - Effectiveness of intravenous fosnetupitant & palonosetron for cinv prophylaxis in patients receiving highly emetogenic chemotherapy regimens: Subgroup analysis from a phase IV Indian studyPresenter: Arun Kumar Verma Session: Poster session 12 1880P - Antiemetic prophylaxis during chemoradiation: Sub-study of the GAND-emesis trial identifying dosimetric predictors for vomitingPresenter: Anika Johannsdottir Session: Poster session 12 1881P - Enhancing chemotherapy-induced nausea and vomiting management: Insights into guideline adherence and patient outcomesPresenter: Suresh Attili Session: Poster session 12 1882P - Awareness of chemotherapy induced nausea and vomiting and adherence to guidelines: A multinational and multicenter surveyPresenter: Ricardo Caponero Session: Poster session 12 1883P - Impact of geriatrician-implemented Interventions on chemotherapy (CT) delivery in vulnerable elderly patients with early or advanced solid tumors: The GIVE trialPresenter: Emanuela Risi Session: Poster session 12 1884P - Development and validation of a prediction tool for severe treatment-related toxicities in older cancer patients on systemic treatment (TR-TRM)Presenter: Wendy Chan 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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