Periampullary malignant neoplasms are among the most lethal gastrointestinal tumors. They are usually diagnosed at advanced stages and require complex surgical treatment. Pancreaticoduodenectomy, the standard procedure for resectable cases, significantly impacts nutritional status, pancreatic function, and the structural integrity of the remaining pancreas. However, there are still significant knowledge gaps regarding the volumetric and molecular changes that occur postoperatively and how these changes interact with body composition, resting energy expenditure, and biochemical markers. This prospective, controlled, cohort study aims to integrate clinical, nutritional, metabolic, molecular, and imaging data to investigate changes in the remnant pancreas and their associations with postoperative outcomes. The study is expected to provide novel insights to support personalized, evidence-based nutritional and metabolic care for patients undergoing pancreaticoduodenectomy.
Periampullary malignant neoplasms are lethal gastrointestinal tumors that are often diagnosed at advanced stages and require complex surgical intervention. Pancreaticoduodenectomy, the gold standard for resectable disease, has profound effects on nutritional status, exocrine pancreatic function, and the structural integrity of the remaining pancreas. Despite recent advances, significant gaps remain in our understanding of the volumetric and molecular alterations that occur postoperatively and how these alterations interact with body composition, resting energy expenditure, and biochemical markers. This is a prospective, longitudinal, controlled, clinical-translational cohort study. Data on clinical, nutritional, biochemical, and plasma parameters will be collected at three time points for the experimental group (preoperatively and 3 and 6 months after hospital discharge) and one time point for the control group. Plasma samples will be stored at -80 °C and analyzed using validated techniques, including multiplex assays, spectrophotometry, ELISA, and tandem mass spectrometry (LC-MS/MS) to detect inflammatory biomarkers (IL-1β, , IL-6, TNF-α, and MCP-1; oxidative markers (MDA, GSH, TAC, and FRAP); proteomic targets (HSP70, fibronectin, and laminin); and lipidomic profiles (ceramides, sphingolipids, and cardiolipins). Abdominal imaging (CT and/or MRI) will be processed using 3D Slicer software to estimate the volume of the remnant pancreas via three-dimensional segmentation. Statistical analyses will be conducted in RStudio. We will apply mixed linear models (MLM and MLMG), incorporating fixed and random effects to account for intra- and inter-individual variability. Missing not-at-random data will be addressed using multiple imputation by chained equations (MICE), and pooled estimates will be calculated according to Rubin's rules. We will set statistical significance at p \< 0.05 with Holm-Bonferroni correction for multiple comparisons. This integrative approach ensures methodological rigor, bias control, and robust inference. It has the potential to guide personalized, evidence-based nutritional strategies in the context of pancreatic cancer.
Study Type
OBSERVATIONAL
Enrollment
44
Pancreaticoduodenectomy (classic Whipple or pylorus-preserving) performed as part of standard clinical care for patients with periampullary malignant neoplasms. This procedure is not assigned by the study protocol, but is the exposure of interest. The study observes nutritional, metabolic, molecular, and imaging outcomes at baseline (preoperative), and at 3 and 6 months after hospital discharge.
Ribeirão Preto Medical School University of São Paulo
Ribeirão Preto, São Paulo, Brazil
Resting Energy Expenditure (REE) in kcal/day
Resting energy expenditure will be measured using indirect calorimetry (Quark RMR®) following standardized protocols. Results will be expressed in kcal/day, and normalized to body weight and fat-free mass. Results will be compared with predictive equations (Harris-Benedict, Mifflin-St Jeor, FAO/WHO).
Time frame: Day 0 (preoperative), 3 months post-discharge, and 6 months post-discharge
Fat-Free Mass (kg) measured by multifrequency bioimpedance analysis
Fat-free mass will be assessed using multifrequency bioimpedance (SECA mBCA 525®). Values will be reported in kilograms and normalized by body surface area.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Fat Mass (kg) measured by multifrequency bioimpedance analysis
Fat mass will be measured using SECA mBCA 525® bioimpedance. Results will be expressed in kilograms and monitored across study visits.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Hydration Status (%) assessed by bioimpedance analysis
Percentage of total body water will be determined by SECA mBCA 525® device using multifrequency bioimpedance.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Phase Angle (°) assessed by bioimpedance analys
Phase angle will be derived from resistance and reactance using multifrequency BIA with SECA mBCA 525®, as a proxy of cell membrane integrity.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Total Serum Protein (g/dL)
Measured using colorimetric assay with spectrophotometric reading at 540 nm. Reference range: 6.0-8.3 g/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Albumin (g/dL)
Quantified using specific colorimetric method with reading at 625 nm. Normal range: 3.5-5.0 g/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum C-Reactive Protein - CRP (mg/L)
Systemic inflammation marker measured via immunoturbidimetric assay with latex particles. Reference value: \<3 mg/L.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Fasting Glucose (mg/dL)
Measured by enzymatic colorimetric method. Reference range: 70-99 mg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Hemoglobin (g/dL)
Determined by automated hematology analyzer (ABX Pentra DX120), using impedance, photometry, and fluorescence. Reference: 13-17.5 g/dL (men), 12-15.5 g/dL (women).
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Absolute Lymphocyte Count (×10³/mm³)
Analyzed using automated hematology analyzer. Normal range: 1.0-4.0 ×10³/mm³.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Iron (µg/dL)
Determined by direct colorimetric method. Normal range: 65-175 µg/dL (men), 50-170 µg/dL (women).
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Ferritin (ng/mL)
Measured by chemiluminescence (Immulite 2000). Normal: 30-300 ng/mL (men), 15-150 ng/mL (women).
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Latent Iron-Binding Capacity - LIBC (µg/dL)
Assessed via direct colorimetric method. Reference: 240-450 µg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Transferrin (mg/dL)
Calculated using Vannucchi et al. (1996): Transferrin = ((LIBC + Iron) × 0.8) - 43. Reference: 200-360 mg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Transferrin Saturation (%)
Calculated by serum iron / LIBC ratio. Normal range: 20-50%.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Urea (mg/dL)
Measured using kinetic method and spectrophotometric reading at 340 nm. Reference: 10-40 mg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Creatinine (mg/dL)
Quantified by kinetic method with reading at 500 nm. Reference: 0.7-1.3 mg/dL (men), 0.6-1.1 mg/dL (women).
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
AST (U/L)
Aspartate aminotransferase assessed via optimized UV method. Normal range: 10-40 U/L.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
ALT (U/L)
Alanine aminotransferase determined by UV method at 340 nm. Reference: 7-56 U/L.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Folate - Vitamin B9 (ng/mL)
Measured by chemiluminescence (Immulite 2000). Reference: 3.0-17.0 ng/mL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Serum Vitamin B12 (pg/mL)
Cobalamin levels determined by chemiluminescence. Normal range: 200-900 pg/mL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Vitamin A - Retinol (µg/dL)
Determined by HPLC. Reference: 30-80 µg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Vitamin E - Alpha-tocopherol (mg/dL)
Assessed by HPLC. Normal range: 0.5-2.0 mg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Copper (µg/dL)
Measured by atomic absorption spectroscopy at 327.4 nm. Reference: 70-140 µg/dL (men), 80-155 µg/dL (women).
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Zinc (µg/dL)
Determined via atomic absorption spectroscopy at 213.9 nm. Reference: 60-120 µg/dL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Sudan III Stool Test (qualitative)
Microscopic evaluation of Sudan III-stained stool samples for detection of steatorrhea. Reported as positive or negative.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Interleukin 1 beta (IL-1β), pg/mL
Plasma concentrations will be quantified using a multiplex immunoassay with magnetic beads (MagPix®, Luminex Corporation), following manufacturer's specifications.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Interleukin 4 (IL-4), pg/mL
Quantified via bead-based multiplex fluorescence assay using the MagPix® system (Luminex®), allowing simultaneous detection of multiple cytokines.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Interleukin 6 (IL-6), pg/mL
Measured by high-sensitivity magnetic bead-based immunoassay (Luminex® MagPix®), using standard calibration curves.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Interleukin 8 (IL-8), pg/mL
Determined using multiplex fluorescence-based immunoassay with magnetic bead differentiation and spectral laser detection.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Interleukin 10 (IL-10), pg/mL
Plasma levels will be assessed using a validated multiplex Luminex® panel, enabling parallel cytokine detection.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Tumor Necrosis Factor Alpha (TNF-α), pg/mL
Measured by multiplex immunoassay with magnetic beads on the Luminex® platform; assay sensitivity \<1 pg/mL.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Interferon Gamma (INF-γ), pg/mL
Quantified using bead-based multiplex immunoassay with MagPix® system and fluorophore-labeled secondary antibodies.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Vascular Endothelial Growth Factor (VEGF), pg/mL
Determined by multiplex immunoassay using magnetic beads, with detection by Luminex® MagPix® laser-based fluorescence reader.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Monocyte Chemoattractant Protein 1 (MCP-1), pg/mL
Assessed using a Luminex®-based multiplex immunoassay with internal controls and duplicate sampling.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Free Plasma Amino Acids (HPLC), nmol/mL
Quantified by high-performance liquid chromatography (HPLC) with pre-column derivatization using o-phthaldialdehyde (OPA) and fluorescence detection (excitation: 340 nm; emission: 450 nm).
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Malondialdehyde (MDA), nmol/mL
Measured by the thiobarbituric acid reactive substances (TBARS) assay, with spectrophotometric reading at 532 nm.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Reduced Glutathione (GSH), µmol/L
Quantified by spectrophotometric method using DTNB (5,5'-dithiobis-(2-nitrobenzoic acid)), with absorbance measured at 412 nm.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Total Hydroperoxides (FOX), µmol/L
Measured using the Ferrous Oxidation-Xylenol Orange (FOX) method with absorbance at 560 nm.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Total Antioxidant Capacity (TAC), mmol/L
Assessed using the ABTS+ radical cation decolorization assay with spectrophotometric analysis.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Ferric Reducing Ability of Plasma (FRAP), mmol/L
Quantified using the FRAP assay, based on the reduction of Fe3+ to Fe2+, measured at 593 nm.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Heat Shock Protein 70 (HSP70), ng/mL
Plasma concentrations will be measured using sandwich-type enzyme-linked immunosorbent assay (ELISA), with detection at 450 nm after chromogenic substrate reaction.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Fibronectin, µg/mL
Quantified by high-sensitivity ELISA using monoclonal antibodies specific for fibronectin. Detection will be performed at 450 nm, using manufacturer-calibrated standard curves.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Laminin, µg/mL
Determined by validated ELISA sandwich assay with photometric quantification at 450 nm. Assay will be conducted in duplicate with quality controls and external calibrators.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Ceramides, ng/mL
Quantified using liquid chromatography-tandem mass spectrometry (LC-MS/MS) after lipid extraction via the Folch method. Identification and quantification will be based on retention times and certified external standards.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Sphingolipids, ng/mL
Plasma concentrations will be determined using validated LC-MS/MS protocols with external calibrators, after sample preparation by chloroform/methanol extraction.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Cardiolipins, ng/mL
Quantified by LC-MS/MS using C18 chromatographic separation and tandem MS detection, with identification based on spectral patterns and standard curves.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Prostaglandins, pg/mL
Determined by LC-MS/MS with high-sensitivity detection and external calibration for absolute quantification. Sample preparation follows established lipidomic protocols.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Plasma Leukotrienes, pg/mL
Measured using targeted LC-MS/MS following Folch lipid extraction. Identification and quantification will be conducted against authentic leukotriene standards.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
Pancreatic Remnant Volume, cm³
The remnant pancreatic volume will be measured using computed tomography (CT) and/or magnetic resonance imaging (MRI). Volumetric analysis will be performed through three-dimensional segmentation using 3D Slicer software.
Time frame: Day 0 (preoperative), 3 months post-discharge, 6 months post-discharge
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