| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Babiker, Hani M. |
| dc.contributor.author | Picozzi, Vincent J. |
| dc.contributor.author | Chandana, Sreenivasa R |
| dc.contributor.author | Melichar, Bohuslav |
| dc.contributor.author | Kasi, Anup |
| dc.contributor.author | Gang, Jin |
| dc.contributor.author | Macarulla, Teresa |
| dc.date.accessioned | 2025-08-11T06:53:29Z |
| dc.date.available | 2025-08-11T06:53:29Z |
| dc.date.issued | 2025-07-20 |
| dc.identifier.citation | Babiker 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.issn | 1527-7755 |
| dc.identifier.uri | http://hdl.handle.net/11351/13513 |
| dc.description | Gemcitabine; Locally advanced pancreatic adenocarcinoma |
| dc.description.abstract | Purpose
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.iso | eng |
| dc.publisher | American Society of Clinical Oncology |
| dc.relation.ispartofseries | Journal of Clinical Oncology;43(21) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Adenocarcinoma - Tractament |
| dc.subject | Pàncrees - Càncer - Tractament |
| dc.subject | Quimioteràpia combinada |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
| dc.subject.mesh | Adenocarcinoma |
| dc.subject.mesh | Pancreatic Neoplasms |
| dc.subject.mesh | /drug therapy |
| dc.title | Tumor Treating Fields With Gemcitabine and Nab-Paclitaxel for Locally Advanced Pancreatic Adenocarcinoma: Randomized, Open-Label, Pivotal Phase III PANOVA-3 Study |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1200/JCO-25-00746 |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
| dc.subject.decs | adenocarcinoma |
| dc.subject.decs | neoplasias pancreáticas |
| dc.subject.decs | /farmacoterapia |
| dc.relation.publishversion | https://doi.org/10.1200/JCO-25-00746 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 40448572 |
| dc.identifier.wos | 001525905900001 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |