Publication:
Bintrafusp Alfa, a Bifunctional Fusion Protein Targeting TGF-β and PD-L1, in Second-Line Treatment of Patients With NSCLC: Results From an Expansion Cohort of a Phase 1 Trial.

dc.contributor.authorPaz-Ares, Luis
dc.contributor.authorKim, Tae Min
dc.contributor.authorVicente, David
dc.contributor.authorFelip, Enriqueta
dc.contributor.authorLee, Dae Ho
dc.contributor.authorLee, Ki Hyeong
dc.contributor.authorLin, Chia-Chi
dc.contributor.authorFlor, Maria Jose
dc.contributor.authorDi Nicola, Massimo
dc.contributor.authorAlvarez, Rosa Maria
dc.contributor.authorDussault, Isabelle
dc.contributor.authorHelwig, Christoph
dc.contributor.authorOjalvo, Laureen S
dc.contributor.authorGulley, James L
dc.contributor.authorCho, Byoung Chul
dc.date.accessioned2023-02-08T14:43:17Z
dc.date.available2023-02-08T14:43:17Z
dc.date.issued2020-03-13
dc.description.abstractThe safety and efficacy of bintrafusp alfa, a first-in-class bifunctional fusion protein composed of the extracellular domain of the transforming growth factor β (TGF-β) receptor II (a TGF-β "trap") fused to a human immunoglobulin G1 antibody blocking programmed death-ligand 1 (PD-L1), was evaluated in patients with advanced NSCLC. This expansion cohort of NCT02517398, an ongoing, phase 1, open-label trial, includes 80 patients with advanced NSCLC that progressed after platinum doublet therapy or after platinum-based adjuvant or neoadjuvant treatment and those who also have not received previous immunotherapy. Patients were randomized at a one-to-one ratio to receive either bintrafusp alfa 500 mg or the recommended phase 2 dosage of 1200 mg every 2 weeks. The primary end point was the best overall response (by Response Evaluation Criteria in Solid Tumors 1.1 as adjudicated by independent review committee) and was assessed by the objective response rate (ORR). A total of 80 patients were randomized to receive bintrafusp alfa 500 or 1200 mg (n = 40 each). Median follow-up was 51.9 weeks (IQR, 19.6-74.0). The ORR in all patients was 21.3% (17 of 80). The ORR was 17.5% (seven of 40) and 25.0% (10 of 40) for the 500 mg dose and the 1200 mg dose (recommended phase 2 dose), respectively. At the 1200 mg dose, patients with PD-L1-positive and PD-L1-high (≥80% expression on tumor cells) had ORRs of 36.0% (10 of 27) and 85.7% (six of seven), respectively. Treatment-related adverse events occurred in 55 of the 80 patients (69%) and were graded as greater than or equal to 3 in 23 of the 80 patients (29%). Of the 80 patients, eight (10%) had a treatment-related adverse event that led to treatment discontinuation; no treatment-related deaths occurred. Bintrafusp alfa had encouraging efficacy and manageable tolerability in patients with NSCLC previously treated with platinum.
dc.identifier.doi10.1016/j.jtho.2020.03.003
dc.identifier.essn1556-1380
dc.identifier.pmcPMC8210474
dc.identifier.pmid32173464
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210474/pdf
dc.identifier.unpaywallURLhttp://www.jto.org/article/S1556086420301957/pdf
dc.identifier.urihttp://hdl.handle.net/10668/15241
dc.issue.number7
dc.journal.titleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
dc.journal.titleabbreviationJ Thorac Oncol
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationHospital Universitario Virgen Macarena
dc.page.number1210-1222
dc.pubmedtypeClinical Trial, Phase I
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subjectBintrafusp alfa
dc.subjectM7824
dc.subjectNSCLC
dc.subjectPD-L1
dc.subjectTGF-β
dc.subject.meshAntibodies, Monoclonal
dc.subject.meshB7-H1 Antigen
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshTransforming Growth Factor beta
dc.titleBintrafusp Alfa, a Bifunctional Fusion Protein Targeting TGF-β and PD-L1, in Second-Line Treatment of Patients With NSCLC: Results From an Expansion Cohort of a Phase 1 Trial.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number15
dspace.entity.typePublication

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