dc.contributor
Institut Català de la Salut
dc.contributor
[Sánchez-Iglesias JL, Pérez-Benavente A, Gil-Moreno A] Unitat de Ginecologia Oncològica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca Biomèdica en Ginecologia, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Morales-Coma C] Unitat de Patologia Mamària, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Minig L] Department of Gynecologic Oncology, IMED Hospital, Valencia, Spain. Department of Gynecology, CEU Cardenal Herrera University, Valencia, Spain. [Lago V] Department of Gynecology, CEU Cardenal Herrera University, Valencia, Spain. Department of Gynecologic Oncology, La Fe University Hospital, Valencia, Spain. [Domingo S] Department of Gynecologic Oncology, La Fe University Hospital, Valencia, Spain. [Mancebo G] Gynecological Cancer Multidisciplinary Unit, Hospital del Mar, Barcelona, Spain. Department of Gynecology, Universitat Pompeu Fabra, Barcelona, Spain. [Gómez-Hidalgo NR, Acosta Ú, Bradbury M] Unitat de Ginecologia Oncològica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Ferrer-Costa R] Servei de Bioquímica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.contributor
Vall d'Hebron Barcelona Hospital Campus
dc.contributor.author
Minig, Lucas
dc.contributor.author
Mancebo Moreno, Gemma
dc.contributor.author
Acosta, Úrsula
dc.contributor.author
Bradbury, Melissa
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Sanchez Iglesias, Jose Luis
dc.contributor.author
Morales Comas, Clara
dc.contributor.author
LAGO, VICTOR
dc.contributor.author
Domingo, Santiago
dc.contributor.author
Rodriguez Gomez-Hidalgo, Natalia
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Ferrer Costa, Roser
dc.contributor.author
PEREZ BENAVENTE, ASUNCION
dc.contributor.author
Gil-Moreno, Antonio
dc.date.accessioned
2024-06-18T14:05:21Z
dc.date.available
2024-06-18T14:05:21Z
dc.date.issued
2024-06-17T06:21:20Z
dc.date.issued
2024-06-17T06:21:20Z
dc.identifier
Sánchez-Iglesias JL, Morales-Coma C, Minig L, Lago V, Domingo S, Mancebo G, et al. Procalcitonin and C-reactive protein as early markers of anastomotic leakage in intestinal resections for advanced ovarian cancer (EDMOCS). Acta Obstet Gynecol Scand. 2024 Jul;103(7):1302–10.
dc.identifier
https://hdl.handle.net/11351/11593
dc.identifier
10.1111/aogs.14834
dc.identifier
001190903900001
dc.identifier.uri
http://hdl.handle.net/11351/11593
dc.description.abstract
Anastomotic leakage; Colorectal resection; Ovarian cancer
dc.description.abstract
Fuga anastomòtica; Resecció colorectal; Càncer d'ovaris
dc.description.abstract
Fuga anastomótica; Resección colorrectal; Cáncer de ovarios
dc.description.abstract
Introduction
Serum levels of procalcitonin and C-reactive protein (CRP) have been used to predict anastomotic leakage after colorectal surgery, but information is scarce in advanced ovarian cancer (AOC) surgery with bowel resection. This study aimed to assess the predictive value of procalcitonin and CRP in detecting anastomotic leakage after AOC surgery with bowel resection. The study also aimed to determine the optimal postoperative reference values and the best day for evaluating these markers.
Material and methods
This prospective, observational and multicentric trial included 92 patients with AOC undergoing debulking surgery with bowel resection between 2017 and 2020 in 10 reference hospitals in Spain. Procalcitonin and CRP levels were measured at baseline and on postoperative days 1–6. Receiver operating characteristic analysis was performed to evaluate the predictive value of procalcitonin and CRP at each postoperative day. Sensitivity, specificity, positive and negative predictive values were calculated.
Results
Anastomotic leakage was detected in six patients (6.5%). Procalcitonin and CRP values were consistently higher in patients with anastomotic leakage at all postoperative days. The maximum area under the curve (AUC) for procalcitonin was observed at postoperative day 1 (AUC = 0.823) with a cutoff value of 3.8 ng/mL (83.3% sensitivity, 81.3% specificity). For CRP, the maximum AUC was found at postoperative day 3 (AUC = 0.833) with a cutoff level of 30.5 mg/dL (100% sensitivity, 80.4% specificity).
Conclusions
Procalcitonin and C-reactive protein are potential biomarkers for early detection of anastomotic leakage after ovarian cancer surgery with bowel resection. Further prospective studies with a larger sample size are needed to confirm these findings.
dc.description.abstract
The study received funding from Vall d'Hebron Research Institute (VHIR) for statistical analysis and medical writing support that was provided by Francisco López de Saro (Trialance SCCL).
dc.format
application/pdf
dc.relation
Acta Obstetricia et Gynecologica Scandinavica;103(7)
dc.relation
https://doi.org/10.1111/aogs.14834
dc.rights
Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Marcadors bioquímics
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Ovaris - Càncer - Cirurgia
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Proteïna C reactiva
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Hormones peptídiques
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DISEASES::Neoplasms::Neoplasms by Site::Endocrine Gland Neoplasms::Ovarian Neoplasms
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Other subheadings::Other subheadings::Other subheadings::/surgery
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CHEMICALS AND DRUGS::Amino Acids, Peptides, and Proteins::Proteins::Albumins::C-Reactive Protein
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CHEMICALS AND DRUGS::Hormones, Hormone Substitutes, and Hormone Antagonists::Hormones::Peptide Hormones::Procalcitonin
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CHEMICALS AND DRUGS::Biological Factors::Biomarkers
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ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de las glándulas endocrinas::neoplasias ováricas
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Otros calificadores::Otros calificadores::Otros calificadores::/cirugía
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COMPUESTOS QUÍMICOS Y DROGAS::aminoácidos, péptidos y proteínas::proteínas::albúminas::proteína C reactiva
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COMPUESTOS QUÍMICOS Y DROGAS::hormonas, sustitutos de hormonas y antagonistas de hormonas::hormonas::hormonas peptídicas::procalcitonina
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COMPUESTOS QUÍMICOS Y DROGAS::factores biológicos::biomarcadores
dc.title
Procalcitonin and C-reactive protein as early markers of anastomotic leakage in intestinal resections for advanced ovarian cancer (EDMOCS)
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion