dc.rights.license | open | en_US |
hal.structure.identifier | Institut Bergonié [Bordeaux] | |
hal.structure.identifier | Université de Bordeaux [UB] | |
dc.contributor.author | ITALIANO, Antoine | |
hal.structure.identifier | Explicyte Immuno-Oncology [Bordeaux] | |
dc.contributor.author | GUEGAN, Jean-Philippe | |
hal.structure.identifier | Institut Universitaire du Cancer de Toulouse - Oncopole [IUCT Oncopole - UMR 1037] | |
dc.contributor.author | VALENTIN, Thibaud | |
hal.structure.identifier | Département d’Innovation Thérapeutique et essais précoces [Gustave Roussy] [DITEP] | |
dc.contributor.author | BAHLEDA, Rastilav | |
hal.structure.identifier | Hôpital Morvan - CHRU de Brest [CHU - BREST ] | |
dc.contributor.author | METGES, Jean Philippe | |
hal.structure.identifier | Centre Léon Bérard [Lyon] | |
dc.contributor.author | CASSIER, Philippe Alexandre | |
hal.structure.identifier | Institut Bergonié [Bordeaux] | |
dc.contributor.author | TOULMONDE, Maud | |
hal.structure.identifier | Institut Bergonié [Bordeaux] | |
dc.contributor.author | SPALATO-CERUSO, Mariella | |
hal.structure.identifier | Institut Bergonié [Bordeaux] | |
hal.structure.identifier | Université de Bordeaux [UB] | |
dc.contributor.author | PEYRAUD, Florent | |
hal.structure.identifier | Institut Bergonié [Bordeaux] | |
dc.contributor.author | PALUSSIÈRE, Jean | |
hal.structure.identifier | Institut Bergonié [Bordeaux] | |
dc.contributor.author | KIND, Michèle | |
hal.structure.identifier | Bordeaux population health [BPH] | |
dc.contributor.author | CANTAREL, Coralie | |
hal.structure.identifier | Bordeaux population health [BPH] | |
dc.contributor.author | BELLERA, Carine | |
hal.structure.identifier | ImmuSmol | |
dc.contributor.author | BESSEDE, Alban | |
dc.date.accessioned | 2024-09-17T12:38:36Z | |
dc.date.available | 2024-09-17T12:38:36Z | |
dc.date.created | 2024-06-01 | |
dc.date.conference | 2024-05-31 | |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/201626 | |
dc.description.abstractEn | 11516 Background: Vascular Endothelial Growth Factor (VEGF)-driven angiogenesis is a pivotal factor in creating an immunosuppressive tumor microenvironment. Approximately 80% of Soft Tissue Sarcomas (STS) are characterized by a 'cold' microenvironment, lacking tertiary lymphoid structures (TLS). While the efficacy of VEGF pathway and PD-1/PD-L1 axis blockade has been established in various tumor types, their impact on 'cold' STS remains unexplored. This study aims to evaluate the synergistic effect of anti-angiogenesis and PD-1 blockade in altering the microenvironment of cold STS, potentially enhancing immune response and therapeutic efficacy. Methods: In this phase II, single-arm, open-label, multicentric trial, we explored the efficacy and safety of combining regorafenib (R) and avelumab (A) in advanced TLS-negative STS patients. Patients were administered 160 mg of R daily for 3 weeks in a 4-week cycle, alongside 10 mg/kg of A biweekly. Endpoints included high-throughput analysis of tumor and plasma samples, response rate, progression-free survival (PFS), overall survival (OS), and safety, as per the NCI-CTCAE v5.0 guidelines. Results: From May 2019 to August 2021, 49 TLS-negative STS patients were enrolled, including leiomyosarcoma (45%), synovial sarcoma (18%), and other subtypes. The median age was 57.1 years, with patients having undergone an average of 2 prior treatment lines. High-throughput analysis of sequential plasma samples indicated an upregulation of immune-inducing protein biomarkers such as CXCL10 and soluble CD8 antigen. Multiplex immunofluorescence analysis of sequential tumor samples revealed significant increase in CD8 T cell infiltration on-treatment. The most common severe adverse events were grade 1 or 2 palmar-plantar erythrodysesthesia, fatigue, and diarrhea. The median follow-up was 7.1 months, with 32.6% of patients experiencing tumor shrinkage, and a clinical benefit rate of 48.8%. The 6-month PFS was 22.1%, with a median OS of 15.1 months. Conclusions: The combination of regorafenib and avelumab demonstrates a marked mobilization of antitumor immunity in patients with TLS-negative STS. The observed efficacy appears superior to that of single-agent immune checkpoint inhibition in 'cold' STS, and higher than the 6-month PFS benchmark of 14% set by EORTC. This indicates the potential effectiveness of this treatment combination in managing advanced cold STS, marking a significant stride in precision immunotherapy for this group of tumors. Clinical trial information: NCT03475953 . | |
dc.language.iso | EN | en_US |
dc.title.en | Reshaping the tumor microenvironment of cold soft-tissue sarcomas with anti-VEGFR targeted therapy: A Phase 2 Trial of Regorafenib combined with avelumab. | |
dc.type | Poster | en_US |
dc.identifier.doi | 10.1200/JCO.2024.42.16_suppl.11516 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Cancer | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Immunologie/Immunothérapie | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Médecine humaine et pathologie | en_US |
bordeaux.hal.laboratories | Bordeaux Population Health Research Center (BPH) - UMR 1219 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.conference.title | American society of clinical oncology Annual meeting 2024 | en_US |
bordeaux.country | us | en_US |
bordeaux.team | EPICENE_BPH | en_US |
bordeaux.conference.city | Chicago | en_US |
bordeaux.import.source | hal | |
hal.identifier | hal-04694549 | |
hal.version | 1 | |
hal.invited | non | en_US |
hal.conference.organizer | American Society of Clinical Oncology (ASCO) | en_US |
hal.conference.end | 2024-06-04 | |
hal.popular | non | en_US |
hal.audience | Internationale | en_US |
hal.export | false | |
workflow.import.source | hal | |
dc.rights.cc | Pas de Licence CC | en_US |
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