Sarcopenia Clinical Trial
Official title:
Influence of Body Composition, Nutritional Status and Inflammatory Markers on Survival and Postoperative Outcome in Patients Operated on for Primary Retroperitoneal Sarcoma: Report From Institute of Oncology Ljubljana
This is a retrospective, observational study in consecutive patients operated on for primary RPS in the Institute of Oncology Ljubljana (Slovenia) between September 1999 and June 2020. This study aims to investigate the impact of preoperatively assessed body composition parameters on the perioperative outcomes of patients operated on for primary RPS. The impact of preoperative malnutrition, sarcopenia, sarcopenic obesity and myosteatosis to the oncologic and postoperative outcome in patients operated on for primary RPS will be examined. Additionally, the aim is to evaluate the prognostic role of preoperative immune and inflammatory markers (serum albumin level, C-reactive protein, neutrophil to lymphocyte ratio, platelet to lymphocyte ratio, high-sensitivity modified Glasgow prognostic score) and prognostic nutritional index in primary RPS patients undergoing surgery. Patient outcome will be evaluated in terms of overall survival (OS), local-recurrence free survival (LRFS), postoperative intrahospital length of stay, overall and major postoperative morbidity.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | December 2023 |
Est. primary completion date | January 2023 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients aged above 18 years old - Patients with primary localized RPS or pelvic sarcoma operated at Surgical Department of Institute of Oncology in Ljubljana Exclusion Criteria: - Patients with Gastrointestinal Stromal Tumors (GISTs) and Retroperitoneal desmoid-type fibromatosis (DF) - Patients with visceral sarcomas (arising from visceral organ i.e., gastrointestinal, and genitourinary tracts sarcoma) - Patients with benign retroperitoneal / pelvic tumors - Patients with residual RPS operated at another hospital - Patients with present recurrent, secondary, and metastatic RPS - Unable to access patients' data |
Country | Name | City | State |
---|---|---|---|
Slovenia | Institute of Oncology Ljubljana | Ljubljana |
Lead Sponsor | Collaborator |
---|---|
Institute of Oncology Ljubljana |
Slovenia,
Arends J, Baracos V, Bertz H, Bozzetti F, Calder PC, Deutz NEP, Erickson N, Laviano A, Lisanti MP, Lobo DN, McMillan DC, Muscaritoli M, Ockenga J, Pirlich M, Strasser F, de van der Schueren M, Van Gossum A, Vaupel P, Weimann A. ESPEN expert group recommendations for action against cancer-related malnutrition. Clin Nutr. 2017 Oct;36(5):1187-1196. doi: 10.1016/j.clnu.2017.06.017. Epub 2017 Jun 23. Review. — View Citation
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Postoperative complications | Complications graded by Clavien-Dindo Complication Classification System | within 30 days after surgery | |
Primary | Local recurrence rate | A postoperative local recurrence will be defined by biopsy-proven or radiographic evidence of local recurrent disease | From date of surgery until the date of first documented local progression assessed until June 2020 | |
Primary | Mortality | Overall survival (OS) will be defined as the time between the date of the operation to the date of death from any cause or last follow-up (according to medical records and using telephone contacts) | Length of survival after surgery until June 2020 (up to 130 months) | |
Secondary | Length of hospital stay | Time interval from the date of operation to the date of discharge. Body composition parameters may predict the length of hospital stay | up to 90 days after surgery | |
Secondary | Major postoperative morbidity | Complication grade 3 or higher according to Clavien-Dindo Complication Classification System | within 90 days after surgery | |
Secondary | Prevalence of preoperative malnutrition in primary RPS patients | A prevalent case of malnutrition will be considered if a patient fulfills the Global Leadership Initiative on Malnutrition (GLIM) criteria. GLIM proposed 5 diagnostic criteria to assess malnutrition and includes 3 phenotypic (weight loss, low body mass index and reduced muscle mass) and 2 etiologic (reduced food intake/assimilation, and inflammation/disease burden) criteria. To diagnose malnutrition at least 1 phenotypic criterion and 1 etiologic criterion should be present | within 30 days before surgery | |
Secondary | Prevalence of preoperative sarcopenia in primary RPS patients | A prevalent case of sarcopenia will be considered if a patient fulfills the diagnostic criteria defined by European Working Group on Sarcopenia in Older People (EWGSOP2) | within 30 days before surgery | |
Secondary | To evaluate the impact of skeletal muscle area (SMA) on the prognosis of patients with primary RPS | Skeletal muscle area (SMA) area will be measured by using preoperative computed tomography (CT) scans at lumbar (L3) vertebral level and recorded as cm^2 using standard Hounsfield Unit thresholds of - 29 to + 150. SMA at the third lumbar spine level has been established as a good indicator of whole-body muscle mass. | through study completion, an average of 6 months | |
Secondary | To evaluate the impact of the muscle radiation attenuation (MRA) on the prognosis of patients with primary RPS | Muscle radiation attenuation (MRA) will be assessed using CT scans at lumbar (L3) vertebral level and recorded as mean Hounsfield unit (HU) of each pixel within a region of interest. MRA reflects muscle composition, including the degree of intramuscular fat accumulation, important to define the presence of myosteatosis | through study completion, an average of 6 months | |
Secondary | To evaluate the impact of visceral adipose tissue (VAT) on the prognosis of patients with primary RPS | Visceral adipose tissue (VAT) area will be measured by using preoperative computed tomography (CT) scans at lumbar (L3) vertebral level and recorded as cm^2 using standard Hounsfield Unit thresholds of -150 to -50 | through study completion, an average of 6 months | |
Secondary | To evaluate the impact of subcutaneous adipose tissue (SAT) on the prognosis of patients with primary RPS | Subcutaneous adipose tissue (SAT) area will be measured by using preoperative computed tomography (CT) scans at lumbar (L3) vertebral level and recorded as cm^2 using standard Hounsfield Unit thresholds of -190 to -30. | through study completion, an average of 6 months | |
Secondary | To evaluate the impact of visceral-to-subcutaneous adipose tissue area ratio (VSR) on the prognosis of patients with primary RPS | Visceral-to-subcutaneous adipose tissue ratio will be calculated by dividing the visceral adipose tissue area by the subcutaneous adipose tissue area. | through study completion, an average of 6 months | |
Secondary | To assess the impact of complete blood count based systemic inflammatory markers: NLR, PLR and SII on the prognosis of patients with primary RPS | Neutrophil to lymphocyte ratio (NLR): calculated as the absolute neutrophil count divided by the absolute lymphocyte count.
Platelet to Lymphocyte Ratio (PLR): calculated as the absolute platelet count divided by the absolute lymphocyte count. Systemic immune inflammation index (SII): based on absolute platelet, neutrophil and lymphocyte count and calculated according to following formula: SII =(platelet count×neutrophil count)/(lymphocyte count) |
within 30 days before surgery | |
Secondary | To assess the preoperative high-sensitivity modified Glasgow prognostic score (Hs-mGPS) and prognostic nutrition index (PNI) as prognostic tools in primary RPS patients | The high-sensitivity modified Glasgow prognostic score (Hs-mGPS) will be defined as numeric value 0 - 2 according to following criteria based on C-reactive protein (CRP) and serum albumin levels:
Score 0: CRP level = 0.3 mg/dl and albumin = 3.5 g/dl, Score 1: CRP level > 0.3 mg/dl and albumin = 3.5 g/dl, Score 3: CRP level > 0.3 mg/ dl and albumin < 3.5 g/dl. The prognostic nutrition index (PNI) will be calculated based on previously published and validated formula: PNI =10× serum albumin (g/dl)+0.005× lymphocyte count (per mm^3) |
within 30 days before surgery |
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