G. Bodoky

ORCID: 0000-0002-5659-2020
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About
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Research Areas
  • Colorectal Cancer Treatments and Studies
  • Gastric Cancer Management and Outcomes
  • Pancreatic and Hepatic Oncology Research
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Cancer Treatment and Pharmacology
  • Lung Cancer Treatments and Mutations
  • Cancer Genomics and Diagnostics
  • Genetic factors in colorectal cancer
  • Neuroendocrine Tumor Research Advances
  • Gastrointestinal Tumor Research and Treatment
  • Colorectal Cancer Surgical Treatments
  • Colorectal and Anal Carcinomas
  • Diet and metabolism studies
  • Esophageal Cancer Research and Treatment
  • Economic and Financial Impacts of Cancer
  • Renal cell carcinoma treatment
  • Clinical Nutrition and Gastroenterology
  • Cancer, Lipids, and Metabolism
  • Lung Cancer Research Studies
  • Pancreatitis Pathology and Treatment
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Multiple and Secondary Primary Cancers
  • Cancer Immunotherapy and Biomarkers
  • Helicobacter pylori-related gastroenterology studies
  • PI3K/AKT/mTOR signaling in cancer

Unified Szent István and Szent László Hospital
2015-2025

Országos Pszichiátriai és Neurológiai Intézet
2022

Roche (Switzerland)
2021

University of Szeged
2021

National Health Research Institutes
2019

Centrum Onkologii
2019

Hungarian Academy of Sciences
2014

Semmelweis University
1989-2014

University of Verona
2014

KU Leuven
2009-2013

We investigated the efficacy of cetuximab plus irinotecan, fluorouracil, and leucovorin (FOLFIRI) as first-line treatment for metastatic colorectal cancer sought associations between mutation status KRAS gene in tumors clinical response to cetuximab.We randomly assigned patients with epidermal growth factor receptor-positive unresectable metastases receive FOLFIRI either alone or combination cetuximab. The primary end point was progression-free survival.A total 599 received FOLFIRI, alone....

10.1056/nejmoa0805019 article EN New England Journal of Medicine 2009-04-01

Patients with metastatic colorectal cancer that harbors KRAS mutations in exon 2 do not benefit from anti–epidermal growth factor receptor (EGFR) therapy. Other activating RAS may also be negative predictive biomarkers for anti-EGFR

10.1056/nejmoa1305275 article EN New England Journal of Medicine 2013-09-11

Panitumumab, a fully human anti-epidermal growth factor receptor (EGFR) monoclonal antibody that improves progression-free survival (PFS), is approved as monotherapy for patients with chemotherapy-refractory metastatic colorectal cancer (mCRC). The Panitumumab Randomized Trial in Combination With Chemotherapy Metastatic Colorectal Cancer to Determine Efficacy (PRIME) was designed evaluate the efficacy and safety of panitumumab plus infusional fluorouracil, leucovorin, oxaliplatin (FOLFOX4)...

10.1200/jco.2009.27.4860 article EN Journal of Clinical Oncology 2010-10-05

Mutations within the KRAS proto-oncogene have predictive value but are of uncertain prognostic in treatment advanced colorectal cancer. We took advantage PETACC-3, an adjuvant trial with 3,278 patients stage II to III colon cancer, evaluate and BRAF tumor mutation status this setting.Formalin-fixed paraffin-embedded tissue blocks (n = 1,564) were prospectively collected DNA was extracted from sections 1,404 cases. Planned analysis exon 2 15 mutations performed by allele-specific real-time...

10.1200/jco.2009.23.3452 article EN Journal of Clinical Oncology 2009-12-15

10.1016/s0140-6736(15)00986-1 article EN The Lancet 2015-11-29

This phase III trial compared the efficacy and safety of gemcitabine (Gem) plus capecitabine (GemCap) versus single-agent Gem in advanced/metastatic pancreatic cancer.Patients were randomly assigned to receive GemCap (oral 650 mg/m2 twice daily on days 1 14 1,000 by 30-minute infusion 8 every 3 weeks) or (1,000 weekly for 7 weeks, followed a 1-week break, then weeks 4 weeks). Patients stratified according center, Karnofsky performance score (KPS), presence pain, disease extent.A total 319...

10.1200/jco.2006.09.0886 article EN Journal of Clinical Oncology 2007-05-30

BackgroundThe Panitumumab Randomized trial In combination with chemotherapy for Metastatic colorectal cancer to determine Efficacy (PRIME) demonstrated that panitumumab–FOLFOX4 significantly improved progression-free survival (PFS) versus FOLFOX4 as first-line treatment of wild-type (WT) KRAS metastatic (mCRC), the primary end point study.Patients and methodsPatients were randomized 1:1 panitumumab 6.0 mg/kg every 2 weeks + (arm 1) or 2). This prespecified final descriptive analysis efficacy...

10.1093/annonc/mdu141 article EN publisher-specific-oa Annals of Oncology 2014-04-10

Purpose Patients with advanced gastric or gastroesophageal adenocarcinoma need more efficacious and safer treatments than established today. S-1, a contemporary oral fluoropyrimidine, can provide that advantage. Methods This study was conducted in 24 countries 146 centers. One thousand fifty-three patients were stratified (center, number of metastatic sites, prior adjuvant therapy, measurable cancer) randomly assigned. received either S-1 at 50 mg/m 2 divided two daily doses for 21 days...

10.1200/jco.2009.25.4706 article EN Journal of Clinical Oncology 2010-02-17

PURPOSE The primary objective of this randomized, multicenter, phase III trial was to investigate whether the addition irinotecan de Gramont infusional fluorouracil (FU)/leucovorin (LV) adjuvant regimen (LV5FU2) would improve disease-free survival (DFS) in patients with stage colon cancer. PATIENTS AND METHODS After curatively intentioned surgery, II and cancer were randomly allocated surgery receive LV5FU2 (LV 200 mg/m(2) as a 2-hour infusion, followed by FU; 400 bolus then 600 continuous...

10.1200/jco.2008.21.6663 article EN Journal of Clinical Oncology 2009-05-19
Charles S. Fuchs Kohei Shitara Maria Di Bartolomeo Sara Lonardi Salah‐Eddin Al‐Batran and 95 more Eric Van Cutsem David H. Ilson María Alsina Ian Chau Jill Lacy Michel Ducreux Guillermo Ariel Mendez Alejandro Molina Alavez Daisuke Takahari Wasat Mansoor Peter C. Enzinger Vera Gorbounova Zev A. Wainberg Susanna Hegewisch‐Becker David Ferry Ji Lin Roberto Carlesi Mayukh Das Manish A. Shah Alexander Luft Nina Karaseva Rubén Dario Kowalyszyn Carlos Alberto Hernández Tibor Csöszi Ferdinando De Vita Per Pfeiffer Naotoshi Sugimoto Judit Kocsis Andràs Csilla G. Bodoky Georgina Garnica Jaliffe Светлана Проценко Ayman Madi Elżbieta Wójcik Baruch Brenner Gunnar Folprecht Tomasz Sarosiek Katriina Peltola Peter Bono Hubert Ayala Giuseppe Aprile Cardellino Giovanni Gerardo Fidel David Huitzil Melendez Alfredo Falcone Francesco Di Costanzo Moustapha Tehfe Laurent Mineur Pilar Alfonso Radka Obermannová Hélène Senellart Russell Petty Leslie Samuel Péter Ács Maen Hussein M. Nechaeva Frans Erdkamp Elizabeth Won Johanna C. Bendell Javier Gállego Sylvie Lorenzen Bohuslav Melichar Miguel Angel Escudero Denis Pezet Jean-Marc Phélip Diego Kaen James A. Reeves Federico Longo Muñoz Srinivasan Madhusudan Carlo Barone Luis Fein Ángel Gómez Villanueva Mohamed Hebbar Jana Prausová L. Visa Turmo J. Vidal Barrull Mette Yilmaz Alex Beny Hanneke W.M. van Laarhoven Brian DiCarlo Taito Esaki Kazumasa Fujitani Karen Geboes Ravit Geva Shigenori Kadowaki Stephen Leong Nozomu Machida Moses S. Raj Francisco Javier Ramirez Godinez Ágnes Ruzsa Hugo Ford William Lawler Nicolas Robert Maisey Jiřı́ Petera Einat Shacham‐Shmueli Isabelle Sinapi

10.1016/s1470-2045(18)30791-5 article EN The Lancet Oncology 2019-02-01
Margaret A. Tempero Uwe Pelzer Eileen M. O’Reilly Jordan M. Winter Do‐Youn Oh and 95 more Chung‐Pin Li Giampaolo Tortora Heung-Moon Chang Charles D. Lopez Tanios Bekaii‐Saab Andrew H. Ko Armando Santoro Joon Oh Park Marcus Smith Noel Giovanni Luca Frassineti Yan‐Shen Shan Andrew Dean Hanno Riess Eric Van Cutsem Jordan Berlin Philip Philip Malcolm J. Moore David Goldstein Josep Tabernero Mingyu Li Stefano Ferrara Yvan Le Bruchec George Zhang Brian Lu Andrew V. Biankin Michele Reni Richard A. Epstein Paul L. Vasey Jeremy Shapiro Matthew Burge Yu Jo Chua Marion Harris Nick Pavlakis Niall C. Tebbutt Gerald W. Prager Christian Dittrich Alois Lang Kathrin Philipp‐Abbrederis Richard Greil Herbert Stöger Michael Girschikofsky Thomas Kuehr Jean–Luc Van Laethem Stéphanie Laurent Neesha C. Dhani Yoo Joung Ko Scot Dowden Petr Kavan Mustapha Édouard Tehfe Eugen Kubala Milan Kohoutek Per Pfeiffer Mette Yilmaz Vibeke Parner Tapio Salminen Leena‐Maija Soveri Eija Korkeila Pia Österlund Julien Taı̈eb David Tougeron Pascal Artru François‐Xavier Caroli‐Bosc Rosine Guimbaud Anthony Turpin Thomas Walter Jean‐Baptiste Bachet Volker Kunzmann Florian Kreth Andreas De Block Marino Venerito Helmut Oettle Meinolf Karthaus Jörg Trojan Gunnar Folprecht Markus M. Lerch Frank Kullmann Marcel Reiser Volker Heinemann Marcus‐Alexander Wörns H. Schulz Benjamin Garlipp Thomas Yau Lam Stephen Chan Balázs Juhász László Landherr Tamàs Pintér G. Bodoky Zsuzsanna Kahán Ray McDermott Derek G. Power Luca Gianni Salvatore Siena Michèle Milella Alfredo Falcone Rossana Berardi

This randomized, open-label trial compared the efficacy and safety of adjuvant

10.1200/jco.22.01134 article EN cc-by-nc-nd Journal of Clinical Oncology 2022-12-15

LBA3 Background: PTK787/ZK 222584 (PTK/ZK) is a novel, oral, small molecule, anti-angiogenesis compound that blocks tyrosine kinase signaling from all known vascular endothelial growth factor (VEGF) receptors. Phase I/II studies of PTK/ZK as single agent showed it safe and well tolerated. Dose response was observed by DCE-MRI. An expanded phase study evaluating escalating doses in combination with oxaliplatin/5-FU/LV first-line therapy metastatic colorectal cancer (CRC) demonstrated...

10.1200/jco.2005.23.16_suppl.lba3 article EN Journal of Clinical Oncology 2005-06-01

To compare the efficacy of cediranib (a vascular endothelial growth factor receptor tyrosine kinase inhibitor [VEGFR TKI]) with that bevacizumab (anti-VEGF-A monoclonal antibody) in combination chemotherapy as first-line treatment for advanced metastatic colorectal cancer (mCRC).HORIZON III [Cediranib Plus FOLFOX6 Versus Bevacizumab Patients With Untreated Metastatic Colorectal Cancer] had an adaptive phase II/III design. randomly assigned 1:1:1 received mFOLFOX6 [oxaliplatin 85 mg/m(2) and...

10.1200/jco.2012.42.5355 article EN Journal of Clinical Oncology 2012-09-11
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