Published December 5, 2025
| Version v1
Journal article
Open
VEGF Signaling Pathway Germline Polymorphisms as Prognostic Pharmacogenetic Biomarkers in Localized High-Grade Osteosarcoma Patients from the GEIS-33 Protocol.
Authors/Creators
- 1. Translational Medical Oncology Laboratory, Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain
- 2. Research Laboratory Unit, Fundació Docència i Recerca Mútua Terrassa, 08221 Terrassa, Spain
- 3. Medical Oncology Department, Hospital Universitario Fundación Jiménez Díaz, 28040 Madrid, Spain
- 4. Osteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies Unit, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy
- 5. Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USA; Osteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies Unit, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy
- 6. Medical Oncology Department, Hospital Universitario Virgen de la Arrixaca, 30120 El Palmar, Spain
- 7. Pediatric Oncology and Hematology Unit, Hospital Universitario y Politécnico La Fe de Valencia, 46026 Valencia, Spain
- 8. Pediatric Hematology and Oncology Department, Hospital Niño Jesús, 28009 Madrid, Spain
- 9. Medical Oncology Department, University Hospital Miguel Servet, 50009 Zaragoza, Spain
- 10. Hospital Regional Universitario de Málaga, 29010 Málaga, Spain
- 11. Pediatric Oncology Group, Pediatrics Department, Hospital Universitario Cruces, 48940 Barakaldo, Spain
- 12. Medical Oncology Department, Hospital Universitario Ramón y Cajal, 28034 Madrid, Spain
- 13. Medical Oncology Department, Complejo Hospitalario Universitario de Santiago de Compostela, 15706 Santiago de Compostela, Spain
- 14. Medical Oncology Department, Hospital Universitario Gregorio Marañón, 28007 Madrid, Spain
- 15. Medical Oncology Department, Vall d'Hebrón Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebrón, 08035 Barcelona, Spain
- 16. Medical Oncology Department, Hospital Universitari Son Espases, 07120 Palma, Spain
- 17. Medical Oncology Department, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain
- 18. Translational Medical Oncology Laboratory, Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain; Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain
Description
Background/Objective: 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. Methods: 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 VEGFA (rs1570360, rs2010963 and rs699947), FLT1 (VEGFR1; rs7993418, rs9513070 and rs9582036), and KDR (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. Results: The analyses showed nominally significant associations between the FLT1 variants rs7993418 and rs9582036 and survival. Patients carrying the rs7993418(C) allele had worse RFS (p = 0.01) and OS (p = 0.01). Carriers of the minor rs9582036(C) allele also had worse RFS (p = 0.02) and OS (p = 0.03). Additionally, patients harboring the TT genotype of the KDR rs1551641 variant had significantly worse RFS (p = 0.002). These polymorphisms remained statistically significant in the multivariate Cox regression analyses that included surgical margins and pathological response as covariates. Conclusions: 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 FLT1 rs7993418 and rs9582036 variants.