<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-07-21T08:08:49Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/26367" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/26367</identifier><datestamp>2025-12-18T12:56:55Z</datestamp><setSpec>com_20.500.12105_19586</setSpec><setSpec>com_20.500.12105_2202</setSpec><setSpec>col_20.500.12105_19587</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Marta Gómez de Cedrón</subfield>
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      <subfield code="a">Juan Moreno-Rubio</subfield>
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      <subfield code="a">Victor de la O Pascual</subfield>
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      <subfield code="a">Beatriz Alvarez</subfield>
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      <subfield code="a">Marta Villarino</subfield>
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      <subfield code="a">María Sereno</subfield>
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      <subfield code="a">César Gómez-Raposo</subfield>
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      <subfield code="a">Silvia Roa</subfield>
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      <subfield code="a">Miriam López Gómez</subfield>
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      <subfield code="a">María Merino-Salvador</subfield>
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      <subfield code="a">Ana Jiménez-Gordo</subfield>
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      <subfield code="a">Sandra Falagán</subfield>
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      <subfield code="a">Cristina Aguayo</subfield>
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      <subfield code="a">Francisco Zambrana</subfield>
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      <subfield code="a">Beatriz Tabarés</subfield>
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      <subfield code="a">Beatriz Garrido</subfield>
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      <subfield code="a">Silvia Cruz-Gil</subfield>
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      <subfield code="a">Cristina M. Fernández Díaz</subfield>
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      <subfield code="a">Lara P. Fernández</subfield>
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      <subfield code="a">Susana Molina</subfield>
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      <subfield code="a">María Carmen Crespo</subfield>
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      <subfield code="a">Youness Ouahid</subfield>
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      <subfield code="a">Juan José Montoya</subfield>
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      <subfield code="a">Ricardo Ramos Ruíz</subfield>
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      <subfield code="a">Guillermo Reglero</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Ana Ramírez de Molina</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Enrique Casado</subfield>
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      <subfield code="c">2025-02-17</subfield>
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      <subfield code="a">Background
Nutrients, including bioactive natural compounds, have been demonstrated to affect key metabolic processes implicated in tumor growth and progression, both in preclinical and clinical trials. Although the application of precision nutrition as a complementary approach to improve cancer treatments is still incipient in clinical practice, the development of powerful “omics” techniques has opened new possibilities for delivering nutritional advice to cancer patients. Precision nutrition may contribute to improving the plasticity and function of antitumor immune responses.

Objectives
Herein, we present the results of a randomized, prospective, longitudinal, double-blind, and parallel clinical trial (NCT05080920) in cancer patients to explore the immune-metabolic effects of a bioactive formula based on diterpenic phenols from rosemary, formulated with bioactive alkylglycerols (Lipchronic© WO/2017/187000). The trial involved cancer patients, including those with lung cancer (LC), colorectal cancer (CRC), and breast cancer (BC), undergoing chemotherapy, targeted biological therapy, and/or immunotherapy. The main readouts of the study were the analysis of Lip on systemic inflammation, hemogram profile, anthropometry, lipid and glucose profiles, and tolerability. Additionally, a deep immune phenotyping of peripheral blood mononuclear cells (PBMCs) was performed to identify the functional effects of Lip on key mediators of the immune system.

Results
Lip was well tolerated. The lung cancer subgroup of patients showed a reduction in biomarkers of systemic inflammation, including the neutrophil-to-lymphocyte ratio (NLR). Furthermore, modulation of key players in the immune system associated with the experimental treatment Lip compared to the control placebo (Pla) treatment was revealed, with particularities among the distinct subgroups of patients. Our results encourage further research to apply molecular nutrition-based strategies as a complementary tool in the clinical management of cancer patients, particularly in the current era of novel immunotherapies.

Clinical trial registration
ClinicalTrials.gov, identifier NCT05080920</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Front Immunol. 2025, 17 Feb</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.3389/fimmu.2025.1519978</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">1664-3224</subfield>
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      <subfield code="a">Frontiers in Immunology</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://hdl.handle.net/20.500.12105/26367</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Randomized clinical trial in cancer patients shows immune metabolic effects exerted by formulated bioactive phenolic diterpenes with potential clinical benefits</subfield>
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