ArticlePloS one2025
Type of pre-existing chronic conditions and their associations with Merkel cell carcinoma (MCC) treatment: Prediction and interpretation using machine learning methods.
Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThis study examined the prevalence of pre-existing chronic conditions and their association with the receipt of specific cancer-directed treatments among older adults with incident primary Merkel Cell Carcinoma (MCC) using novel predictive and interpretable machine learning methods.
methodsWe adopted a retrospective cohort study design with data from linked Surveillance, Epidemiology, and End Results (SEER) registry and Medicare Fee-For-Service claims databases of older adults (≥ 66 years) diagnosed with primary incident MCC between 2008 and 2017. The study cohort consisted of 1,668 older adults with incident MCC and continuous fee-for-service Medicare enrollment for 24 months. Chronic conditions were identified during 12 months before cancer diagnosis date. Type of any MCC treatment (surgery-SRx, radiotherapy-RTx, chemotherapy-CTx, immunotherapy-ITx, and hormonal therapy-HTx) were derived for 12 months following cancer diagnosis. Receipt of any of these treatments and their associations with pre-existing chronic conditions were analyzed using separate eXtreme Gradient Boosting (XGBoost) predictive models and SHapley Additive exPlanations (SHAP) methods.
resultsHigh cholesterol (75.5%), HIV (71.5%), hypertension (67.7%), arthritis (54.9%), coronary artery disease (47.1%), diabetes (43.5%), and hepatitis (37.1%) were some of the highly prevalent pre-existing chronic conditions. MCC treatment varied by type of chronic conditions and treatment modality. For example, a lower percentage of those with hypertension received ITx compared to those without hypertension (5.7% vs. 17.1%). A higher percentage of those with high cholesterol (13.9% vs 10.8%) received HTx compared to those without high cholesterol. XGBoost predictions revealed high predictive accuracy (area under the curve ranged from 0.72 (CTx) to 0.99 (ITx)). Hypertension (ITx), diabetes and thyroid disorders (HTx), congestive heart failure (RTx), and high cholesterol (CTx) were among the top ten predictors of MCC treatment. Congestive heart failure (RTx), hypertension (CTx), heart disease (ITx), thyroid disorders (HTx), and osteoporosis (HTx) positively predicted treatment, whereas high cholesterol (CTx), hypertension (ITx, HTx) and diabetes (ITx, HTx) negatively predicted treatment.
conclusionsPre-existing conditions were highly prevalent among older MCC adults. Cardiovascular and metabolic diseases were the top 10 leading predictors of cancer treatment. However, the associations varied by type of treatment. In spite of the good performance of the model, especially for ITx and HTx, there is a need to replicate these findings using other data sources that provide access to larger population subgroups.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.