VEGF Signaling Pathway Germline Polymorphisms as Prognostic Pharmacogenetic Biomarkers in Localized High-Grade Osteosarcoma Patients from the GEIS-33 Protocol

<b>Background/Objective:</b> The vascular endothelial growth factor (VEGF) signaling pathway induces angiogenesis, which impacts tumor progression and clinical outcomes in patients with localized osteosarcoma. This study evaluates whether genetic polymorphisms in the VEGF signaling pathway are associated with survival outcomes in these patients. <b>Methods:</b> Sixty-nine patients with localized high-grade osteosarcoma enrolled in the GEIS-33 protocol and treated with MAP (methotrexate, doxorubicin, cisplatin) chemotherapy, surgery, and subsequent adjuvant treatment were included. Nine variants of interest in the <i>VEGFA</i> (rs1570360, rs2010963 and rs699947), <i>FLT1</i> (VEGFR1; rs7993418, rs9513070 and rs9582036), and <i>KDR</i> (VEGFR2; rs1551641 and rs1870377 and rs2071559) genes were genotyped from peripheral blood samples using TaqMan Assay technology. Genetic data were correlated with relapse-free survival (RFS) and overall survival (OS) considering clinical variables as covariates. <b>Results:</b> The analyses showed nominally significant associations between the <i>FLT1</i> variants rs7993418 and rs9582036 and survival. Patients carrying the rs7993418(C) allele had worse RFS (<i>p</i> = 0.01) and OS (<i>p</i> = 0.01). Carriers of the minor rs9582036(C) allele also had worse RFS (<i>p</i> = 0.02) and OS (<i>p</i> = 0.03). Additionally, patients harboring the TT genotype of the <i>KDR</i> rs1551641 variant had significantly worse RFS (<i>p</i> = 0.002). These polymorphisms remained statistically significant in the multivariate Cox regression analyses that included surgical margins and pathological response as covariates. <b>Conclusions:</b> Pharmacogenetics may contribute to precision medicine in oncology. Germline polymorphisms in the VEGF pathway may be useful as predictors of survival in high-grade localized osteosarcoma patients treated with chemotherapy, following validation in a large cohort of patients. Current treatment strategies aimed at improving outcomes for osteosarcoma patients may benefit from the identification of new biomarkers, such as these <i>FLT1</i> rs7993418 and rs9582036 variants.

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Pharmaceuticals
Published
2025-12-05
DOI
https://doi.org/10.3390/ph18121855
Primary Topic
Angiogenesis and VEGF in Cancer
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article

VEGF Signaling Pathway Germline Polymorphisms as Prognostic Pharmacogenetic Biomarkers in Localized High-Grade Osteosarcoma Patients from the GEIS-33 Protocol

Ana Sebio, Maitane Andión Catalán, Claudia Valverde, Alexandra Regueiro et al.
Pharmaceuticals
Angiogenesis and VEGF in Cancer
article

VEGF Signaling Pathway Germline Polymorphisms as Prognostic Pharmacogenetic Biomarkers in Localized High-Grade Osteosarcoma Patients from the GEIS-33 Protocol

Ana Sebio, Maitane Andión Catalán, Claudia Valverde, Alexandra Regueiro, Javier Martínez‐Trufero, Javier Martín‐Broto, Massimo Serra, Maria Jesús Arranz, Juliana Salazar, Pilar Blay, Aizpea Echebarria-Barona, Guadalupe Gutierrez, Rosa Álvarez, Jerónimo Martínez, Antonio Juan Ribelles, Emanuela Palmerini, Pablo Luna, María Ángeles Vaz Salgado
article en

Abstract

<b>Background/Objective:</b> The vascular endothelial growth factor (VEGF) signaling pathway induces angiogenesis, which impacts tumor progression and clinical outcomes in patients with localized osteosarcoma. This study evaluates whether genetic polymorphisms in the VEGF signaling pathway are associated with survival outcomes in these patients. <b>Methods:</b> Sixty-nine patients with localized high-grade osteosarcoma enrolled in the GEIS-33 protocol and treated with MAP (methotrexate, doxorubicin, cisplatin) chemotherapy, surgery, and subsequent adjuvant treatment were included. Nine variants of interest in the <i>VEGFA</i> (rs1570360, rs2010963 and rs699947), <i>FLT1</i> (VEGFR1; rs7993418, rs9513070 and rs9582036), and <i>KDR</i> (VEGFR2; rs1551641 and rs1870377 and rs2071559) genes were genotyped from peripheral blood samples using TaqMan Assay technology. Genetic data were correlated with relapse-free survival (RFS) and overall survival (OS) considering clinical variables as covariates. <b>Results:</b> The analyses showed nominally significant associations between the <i>FLT1</i> variants rs7993418 and rs9582036 and survival. Patients carrying the rs7993418(C) allele had worse RFS (<i>p</i> = 0.01) and OS (<i>p</i> = 0.01). Carriers of the minor rs9582036(C) allele also had worse RFS (<i>p</i> = 0.02) and OS (<i>p</i> = 0.03). Additionally, patients harboring the TT genotype of the <i>KDR</i> rs1551641 variant had significantly worse RFS (<i>p</i> = 0.002). These polymorphisms remained statistically significant in the multivariate Cox regression analyses that included surgical margins and pathological response as covariates. <b>Conclusions:</b> Pharmacogenetics may contribute to precision medicine in oncology. Germline polymorphisms in the VEGF pathway may be useful as predictors of survival in high-grade localized osteosarcoma patients treated with chemotherapy, following validation in a large cohort of patients. Current treatment strategies aimed at improving outcomes for osteosarcoma patients may benefit from the identification of new biomarkers, such as these <i>FLT1</i> rs7993418 and rs9582036 variants.

PharmaceuticalsVol. 18(12)
Hebron University (PS), University of Miami (US), Hospital de Sant Pau (ES), Hospital General Universitario Gregorio Marañón (ES), Hospital Universitari i Politècnic La Fe (ES), Complejo Hospitalario Universitario de Santiago (ES), University Hospital Mútua de Terrassa (ES), Hospital Regional Universitario de Málaga (ES), Hospital Infantil Universitario Niño Jesús (ES), Hospital Universitario Miguel Servet (ES), Istituto Ortopedico Rizzoli (IT), Vall d'Hebron Hospital Universitari (ES), Hospital Universitario Fundación Jiménez Díaz (ES), Hospital Universitario Central de Asturias (ES), Hospital de Cruces (ES), Hospital Universitario Virgen de la Arrixaca (ES), Hospital Universitario Son Espases (ES), Sylvester Comprehensive Cancer Center (US), Hospital Universitario Ramón y Cajal (ES), Institut de Recerca Sant Pau (ES)
Openalex Percentile: Top 65%
Angiogenesis and VEGF in Cancer
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