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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorBabiker, Hani M.
dc.contributor.authorPicozzi, Vincent J.
dc.contributor.authorChandana, Sreenivasa R
dc.contributor.authorMelichar, Bohuslav
dc.contributor.authorKasi, Anup
dc.contributor.authorGang, Jin
dc.contributor.authorMacarulla, Teresa
dc.date.accessioned2025-08-11T06:53:29Z
dc.date.available2025-08-11T06:53:29Z
dc.date.issued2025-07-20
dc.identifier.citationBabiker HM, Picozzi V, Chandana SR, Melichar B, Kasi A, Gang J, et al. Tumor Treating Fields With Gemcitabine and Nab-Paclitaxel for Locally Advanced Pancreatic Adenocarcinoma: Randomized, Open-Label, Pivotal Phase III PANOVA-3 Study. J Clin Oncol. 2025 Jul 20;43(21):2350-60.
dc.identifier.issn1527-7755
dc.identifier.urihttp://hdl.handle.net/11351/13513
dc.descriptionGemcitabine; Locally advanced pancreatic adenocarcinoma
dc.description.abstractPurpose Tumor treating fields (TTFields) use alternating electric fields to disrupt cancer cell proliferation. Feasibility of TTFields therapy with gemcitabine/nab-paclitaxel was previously demonstrated in patients with advanced pancreatic adenocarcinoma. PANOVA-3 was designed to confirm safety and efficacy of TTFields in patients with unresectable locally advanced pancreatic adenocarcinoma (LA-PAC). Methods In this global phase III trial, 571 patients with newly diagnosed LA-PAC were randomly assigned to receive gemcitabine 1,000 mg/m2 and nab-paclitaxel 125 mg/m2 by intravenous infusion once a day on days 1, 8, and 15 of a 28-day cycle with or without TTFields. The primary end point was overall survival (OS). Secondary end points included progression-free survival (PFS), local PFS, pain-free survival, and overall response rate (ORR). Distant PFS was analyzed post hoc. Results OS was significantly prolonged using TTFields with gemcitabine/nab-paclitaxel versus gemcitabine/nab-paclitaxel (median, 16.2 months [95% CI, 15.0 to 18.0] v 14.2 months [95% CI, 12.8 to 15.4]; hazard ratio [HR], 0.82 [95% CI, 0.68 to 0.99]; P = .039). PFS, local PFS, and ORR were not improved. Pain-free survival was significantly prolonged with TTFields with gemcitabine/nab-paclitaxel (median, 15.2 months [95% CI, 10.3 to 22.8] v 9.1 months [95% CI, 7.4 to 12.7]; HR, 0.74 [95% CI, 0.56 to 0.97]; P = .027), as was distant PFS (median, 13.9 months [95% CI, 12.2 to 16.8] v 11.5 months [95% CI, 10.4 to 12.9]; HR, 0.74 [95% CI, 0.57 to 0.96]; P = .022). Device-related skin adverse events (AEs) were experienced by 76.3% of patients. Most device-related skin AEs were mild to moderate, with 7.7% of patients reporting a grade 3 AE. Conclusion This study demonstrated significant OS, pain-free survival, and distant PFS benefits for TTFields with gemcitabine/nab-paclitaxel versus gemcitabine/nab-paclitaxel in patients with unresectable LA-PAC, with no additive systemic toxicity.
dc.language.isoeng
dc.publisherAmerican Society of Clinical Oncology
dc.relation.ispartofseriesJournal of Clinical Oncology;43(21)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectAdenocarcinoma - Tractament
dc.subjectPàncrees - Càncer - Tractament
dc.subjectQuimioteràpia combinada
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshAdenocarcinoma
dc.subject.meshPancreatic Neoplasms
dc.subject.mesh/drug therapy
dc.titleTumor Treating Fields With Gemcitabine and Nab-Paclitaxel for Locally Advanced Pancreatic Adenocarcinoma: Randomized, Open-Label, Pivotal Phase III PANOVA-3 Study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1200/JCO-25-00746
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsadenocarcinoma
dc.subject.decsneoplasias pancreáticas
dc.subject.decs/farmacoterapia
dc.relation.publishversionhttps://doi.org/10.1200/JCO-25-00746
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Babiker HM] Mayo Clinic, Jacksonville, FL. [Picozzi V] Virginia Mason Medical Center, Seattle, WA. [Chandana SR] The Cancer & Hematology Centers, Grand Rapids, MI. [Melichar B] Palacky University and University Hospital Olomouc, Olomouc, Czech Republic. [Kasi A] University of Kansas Cancer Center, Kansas City, KS. [Gang J] Changhai Hospital, Shanghai, People’s Republic of China. [Macarulla T] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid40448572
dc.identifier.wos001525905900001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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