Are Calculated Immune Markers with or Without Comorbidities Good Predictors of Colorectal Cancer Survival? The Results of a Longitudinal Study
- Zoltan Herold 1, Magdolna Herold 1, Gyongyver Szentmartoni 1, Reka Szalasy 1, Julia Lohinszky 2, Aniko Somogyi 2, Attila Marcell Szasz 1,3,4, Magdolna Dank 1,3,4
- 1Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1082 Budapest, Hungary.
- 2Department of Internal Medicine and Hematology, Semmelweis University, 1088 Budapest, Hungary.
- 3Department of Medical Oncology, Semmelweis University, 1122 Budapest, Hungary.
- 4National Institute of Oncology, 1122 Budapest, Hungary.
- 0Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1082 Budapest, Hungary.
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View abstract on PubMed
Summary
This summary is machine-generated.Longitudinal evaluation of Pan-immune inflammation value (PIV), prognostic nutritional index (PNI), and systemic immune-inflammation index (SII) in colorectal cancer (CRC) patients reveals their prognostic value. Pathological alterations in these markers over time indicate poor prognosis and aid in early detection.
Area Of Science
- Oncology
- Biomarker Research
- Clinical Pathology
Background
- Prognostic biomarkers for colorectal cancer (CRC) are numerous, yet longitudinal evaluations are scarce.
- Routine laboratory markers offer potential for developing dynamic prognostic tools.
Purpose Of The Study
- To investigate longitudinal changes in biomarkers derived from routine lab tests in CRC patients.
- To assess the relationship between these biomarker changes and comorbidities.
Main Methods
- Retrospective longitudinal observational study of 817 CRC patients with 4542 measurements.
- Calculation of Pan-immune inflammation value (PIV), prognostic nutritional index (PNI), and systemic immune-inflammation index (SII) from complete blood count and albumin data.
Main Results
- Survivors showed stable PIV and SII, and slowly decreasing PNI. Patients with CRC-related death exhibited significantly higher PIV/SII and lower PNI (p < 0.0001).
- Changes in PIV, SII, and PNI towards pathological values were identified as poor prognostic indicators (p < 0.0001).
- Metastasis, chemotherapy, and hypertension significantly influenced these biomarker values.
Conclusions
- PIV, PNI, and SII are suitable for longitudinal monitoring in CRC patients.
- Pathological alterations in these markers over time are valuable prognostic indicators.
- These markers may aid in the early detection of clinicopathological parameters.
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