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Combined Hyperthermic Intraperitoneal Chemotherapy and Normothermic Intraperitoneal Chemotherapy Long-Term After Interval Cytoreduction in Ovarian Cancer: A Phase I Clinical Trial (BICOV1)

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dc.contributor.author González-Gil, Alida
dc.contributor.author Gil-Gómez, Elena
dc.contributor.author Olivares-Ripoll, Vicente
dc.contributor.author Cerezuela-Fernández-de-Palencia, Álvaro
dc.contributor.author Martínez-García, Jerónimo
dc.contributor.author Sánchez-Martínez, Domingo-Antonio
dc.contributor.author Guijarro-Campillo, Alberto-Rafael
dc.contributor.author Cascales-Campos, Pedro-Antonio
dc.date.accessioned 2026-03-09T08:37:06Z
dc.date.available 2026-03-09T08:37:06Z
dc.date.issued 2025-06-12
dc.identifier.citation González-Gil A, Gil-Gómez E, Olivares-Ripoll V, Cerezuela Fernández De Palencia Á, Martínez-García J, Sánchez-Martínez D, et al. Combined Hyperthermic Intraperitoneal Chemotherapy and Normothermic Intraperitoneal Chemotherapy Long-Term After Interval Cytoreduction in Ovarian Cancer: A Phase I Clinical Trial (BICOV1). Cancers. 12 de junio de 2025;17(12):1957. doi:10.3390/cancers17121957
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/25028
dc.description.abstract Backgroud: Ovarian cancer is the deadliest gynecologic malignancy, with most patients presenting with peritoneal dissemination at diagnosis. Complete cytoreduction and sensitivity to platinum-based systemic chemotherapy remain the most significant prognostic factors. However, even after optimal first-line management, over half of patients relapse due to residual microscopic disease. Intraperitoneal chemotherapy aims to target this component, with normothermic intraperitoneal chemotherapy long-term (NIPEC-LT) and hyperthermic intraperitoneal chemotherapy (HIPEC) being the most studied approaches. While NIPEC-LT has demonstrated improved survival in select trials, concerns regarding toxicity and catheter-related complications have limited its adoption as standard care. Conversely, HIPEC has shown survival benefits, particularly in patients undergoing interval cytoreductive surgery (iCRS) after neoadjuvant chemotherapy, leading to its inclusion in clinical guidelines. However, HIPEC is administered as a single intraoperative treatment, limiting its prolonged effect. Objectives and Method: This study investigates the combination of HIPEC and postoperative NIPEC-LT in the BICOV-1 trial, a prospective, non-randomized phase I study evaluating the feasibility, safety, and oncologic outcomes. The primary objective is to assess the treatment completion rates and morbidity. The secondary endpoints include disease-free survival (DFS), overall survival (OS), and quality-of-life measures. Combining HIPEC and NIPEC-LT is a rational approach, as both have shown independent benefits and do not overlap in toxicity. HIPEC-induced biological changes may enhance the effectiveness of subsequent intraperitoneal chemotherapy. This trial will provide essential data for future phase II/III studies assessing the role of intensified intraperitoneal treatment in ovarian cancer management.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es
dc.title Combined Hyperthermic Intraperitoneal Chemotherapy and Normothermic Intraperitoneal Chemotherapy Long-Term After Interval Cytoreduction in Ovarian Cancer: A Phase I Clinical Trial (BICOV1)
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 40563606
dc.relation.publisherversion https://www.mdpi.com/2072-6694/17/12/1957
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.3390/cancers17121957
dc.journal.title Cancers
dc.identifier.essn 2072-6694


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