Mary J. Fidler

ORCID: 0009-0004-9180-8626
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Lung Cancer Treatments and Mutations
  • Cancer Immunotherapy and Biomarkers
  • Lung Cancer Diagnosis and Treatment
  • Lung Cancer Research Studies
  • Head and Neck Cancer Studies
  • Inflammatory Biomarkers in Disease Prognosis
  • Colorectal Cancer Treatments and Studies
  • Radiomics and Machine Learning in Medical Imaging
  • Nutrition and Health in Aging
  • Peptidase Inhibition and Analysis
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Diagnosis and Treatment
  • Gastric Cancer Management and Outcomes
  • Cancer Genomics and Diagnostics
  • Salivary Gland Tumors Diagnosis and Treatment
  • Pancreatic and Hepatic Oncology Research
  • RNA modifications and cancer
  • HER2/EGFR in Cancer Research
  • Ferroptosis and cancer prognosis
  • Cancer, Lipids, and Metabolism
  • Immunotherapy and Immune Responses
  • Multiple and Secondary Primary Cancers
  • Glycosylation and Glycoproteins Research
  • Head and Neck Surgical Oncology
  • Colorectal and Anal Carcinomas

Rush University Medical Center
2016-2025

Rush University
2014-2025

Memorial Sloan Kettering Cancer Center
2022

Genomics England
2020

RELX Group (United States)
2020

University of Chicago
2007-2018

Carolinas Healthcare System
2015

Levine Cancer Institute
2015

Georgetown University
2014

Providence Portland Medical Center
2014

Ezra E.W. Cohen Denis Soulières Christophe Le Tourneau José Dinis Lisa Licitra and 95 more Myung‐Ju Ahn Ainara Soria Jean‐Pascal Machiels Nicolas Mach Ranee Mehra Barbara Burtness Pingye Zhang Jonathan D. Cheng Ramona F. Swaby Kevin J. Harrington Mirelis Acosta-Rivera Douglas R. Adkins Morteza Aghmesheh Myung‐Ju Ahn Mario Airoldi Eduardas Aleknavičius Yousuf Al-Farhat Alain P. Algazi Salah Almokadem Anna Alyasova Jessica R. Bauman Marco Benasso Alfonso Berrocal Victoria Bray Barbara Burtness Francesco Caponigro Ana Castro Terrence P. Cescon Kelvin Chan Arvind Chaudhry Bruno Chauffert Ezra E.W. Cohen Tibor Csöszi Jan Paul de Boer Jean‐Pierre Delord Andreas Dietz José Dinis Charlotte Dupuis Laurence Digue József Erfán Yolanda Escobar Mererid Evans Mary J. Fidler Martin Förster Signe Friesland Apar Kishor Ganti Lionnel Geoffrois Clíona Grant Viktor Gruenwald Kevin J. Harrington Thomas K. Hoffmann Geza Horvai Arturas Inčiūra Raymond Woo-Jun Jang Petra Jankowska Antonio Jimeno Mano Joseph Alejandro Juárez Ramiro Bogusława Karaszewska Andrzej Kawecki Ulrich Keilholz Ulrich Keller Sung‐Bae Kim Judit Kocsis Nuria Kotecki Mark Kozloff J. Lambea László Landherr Yuri Lantsukhay Sergey Lazarev Lip Way Lee Christophe Le Tourneau Lisa Licitra Igor Lifirenko Nicolas Mach Danko Martincic О. В. Маторин Margaret McGrath Jean‐Pascal Machiels Ranee Mehra Krzysztof Misiukiewicz John C. Morris Ф. Ф. Муфазалов Jiaxin Niu Devraj Srinivasan Pedro Pérez Segura Daniel Rauch Maria Leonor Ribeiro Cristina P. Rodriguez Frédéric Rolland Antonio Russo Ágnes Ruzsa Frederico Sanches Sangwon Shin Mikhail Shtiveland

10.1016/s0140-6736(18)31999-8 article EN The Lancet 2018-11-30

Significance Immunotherapy has revolutionized cancer treatment, yielding unprecedented long-term responses and survival. However, a significant proportion of patients remain refractory, which correlates with the absence immune-infiltrated (“hot”) tumors. Here, we observed that FDA-approved unadjuvanted seasonal influenza vaccines administered via intratumoral injection not only provide protection against active virus lung infection, but also reduce tumor growth by increasing antitumor CD8 +...

10.1073/pnas.1904022116 article EN cc-by Proceedings of the National Academy of Sciences 2019-12-30

Abstract Background Recurrent head and neck squamous cell carcinoma (rHNSCC) represents a significant global health burden with an unmet medical need. In this study we determined the safety efficacy of RM‐1929 photoimmunotherapy in patients heavily pretreated rHNSCC. Methods (anti‐EGFR–IR700 dye conjugate) was infused, followed by tumor illumination. We evaluated safety, response, pharmacokinetics. Results Nine were enrolled Part 1 (dose‐finding) 30 2 (safety efficacy). No dose‐limiting...

10.1002/hed.26885 article EN Head & Neck 2021-10-09

BackgroundIn KEYNOTE-010, pembrolizumab versus docetaxel improved overall survival (OS) in patients with programmed death-1 protein (PD)-L1-positive advanced non-small-cell lung cancer (NSCLC). A prespecified exploratory analysis compared outcomes based on PD-L1 expression archival newly collected tumor samples using recently updated data.Patients and methodsPD-L1 was assessed centrally by immunohistochemistry (22C3 antibody) or samples. Patients received 2 10 mg/kg Q3W 75 mg/m2 for 24...

10.1093/annonc/mdy545 article EN publisher-specific-oa Annals of Oncology 2019-01-10

Praluzatamab ravtansine (CX-2009) is a conditionally activated Probody drug conjugate (PDC) comprising an anti-CD166 mAb conjugated to DM4, with protease-cleavable linker and peptide mask that limits target engagement in normal tissue circulation. The tumor microenvironment enriched for proteases capable of cleaving the linker, thereby releasing mask, allowing localized binding CX-2009 CD166. was evaluated phase I/II clinical trial patients advanced solid tumors.Eligible had metastatic...

10.1158/1078-0432.ccr-21-3656 article EN cc-by-nc-nd Clinical Cancer Research 2022-02-11

Immune checkpoint inhibitors (ICIs) have uncommon associations with cardiotoxicity, yet these cardiotoxic effects are associated high mortality. An accurate assessment of risk for cardiotoxicity is essential clinical decision-making, but data from randomized controlled trials often differ real-world observational studies.

10.1161/jaha.123.032620 article EN cc-by-nc-nd Journal of the American Heart Association 2024-05-18

PURPOSE Preclinical studies demonstrated that dual inhibition of epidermal growth factor receptor (EGFR) and vascular endothelial (VEGF) pathways delay the emergence resistance to EGFR tyrosine kinase inhibitors (TKIs), in trials with first-generation TKIs, combination VEGF pathway prolonged progression-free survival (PFS). METHODS The RAMOSE trial (ClinicalTrials.gov identifier: NCT03909334 , HCRN LUN-18-335) is a randomized, open-label multicenter phase II study comparing osimertinib...

10.1200/jco.24.00533 article EN Journal of Clinical Oncology 2024-10-08

The primary objective of this study is to identify prognostic site-specific epigenetic changes in surgically treated Stage I and II nonsmall cell lung cancer (NSCLC) patients by quantifying methylation levels at multiple CpG sites within each gene promoter. Paraffin-embedded tumors from stage Ib, IIa IIb training validation groups 75 57 NSCLC patients, respectively, were analyzed for p16, MGMT, RASSF1, RASSF5, CDH1, LET7, DAPK PTEN promoter hypermethylation. Hypermethylation status was...

10.1002/ijc.24896 article EN International Journal of Cancer 2009-09-30

There is emerging evidence showing a significant relationship between overall survival (OS) in non-small cell lung cancer NSCLC patients and weight change during chemotherapy or chemoradiation. A high neutrophil/lymphocyte ratio (NLR) at baseline follow-up associated with shorter may be surrogate for ongoing inflammation, implicated cachexia tumor progression. The objective of this study to explore potential relationships OS, serial weights, NLRs advanced receiving chemotherapy. One hundred...

10.1186/s12885-017-3122-y article EN cc-by BMC Cancer 2017-02-16

In ADAURA, adjuvant osimertinib significantly improved disease-free survival versus placebo in resected stage IB to IIIA EGFR-mutated NSCLC. We report in-depth analyses of three-year safety, tolerability, and health-related quality life (HRQoL) from ADAURA.Patients were randomized 1:1 80 mg or once daily for up 3 years. Safety assessments performed at baseline, week 2, 4, 12, every 12 weeks until treatment completion discontinuation, 28 days after was stopped. The SF-36 survey measured HRQoL...

10.1016/j.jtho.2023.05.015 article EN cc-by Journal of Thoracic Oncology 2023-05-24

The insulin-like growth factor (IGF) pathway is a complex involving interactions between membrane-bound receptors, ligands, binding proteins, downstream effectors, and other receptor tyrosine kinase signaling cascades. IGF has been identified as potential therapeutic target in non-small cell lung cancer (NSCLC) based on the following provocative factors. Preclinical observations NSCLC have shown that this involved tumor proliferation, survival, invasiveness. In addition, IGF-1R protein...

10.1177/1758834011427576 article EN Therapeutic Advances in Medical Oncology 2011-11-10

The VeriStrat test is a serum proteomic signature originally discovered in non-responders to second line gefitinib treatment and subsequently used predict differential benefit from erlotinib versus chemotherapy previously treated advanced non-small cell lung cancer (NSCLC). Multiple studies highlight the clinical utility of test, however, mechanistic connection between VeriStrat-poor classification poor prognosis untreated patients still an active area research. aim this study was correlate...

10.1186/s12885-018-4193-0 article EN cc-by BMC Cancer 2018-03-20

8509 Background: The PACIFIC trial demonstrated that a year of consolidation PD-(L)1 inhibition following concurrent chemoradiation (CRT) for unresectable stage III NSCLC improves overall survival (OS). optimal duration IO therapy in this setting is undefined. Studies metastatic demonstrate combination PD-(L)1/CTLA-4 OS over chemotherapy alone. This evaluated the use Nivolumab (N) plus Ipilimumab (IPI) or N alone up to 6 months after CRT. Methods: randomized phase II, multicenter 105 pts...

10.1200/jco.2022.40.16_suppl.8509 article EN Journal of Clinical Oncology 2022-06-01

Celecoxib, a cyclooxygenase-2 (COX-2) inhibitor, potentiates antitumor effects of erlotinib in preclinical studies, and COX-2 is frequently expressed non-small cell lung cancer (NSCLC). With these observations, we designed phase II trial to evaluate the efficacy safety plus celecoxib advanced NSCLC.Previously treated stage IIIB/IV NSCLC patients were given at 400 mg orally twice daily 150 until disease progression. Planned accrual was 40 patients. Tissue collected for epidermal growth factor...

10.1158/1078-0432.ccr-07-4013 article EN Clinical Cancer Research 2008-04-01

Definitive chemoradiotherapy is a core treatment modality for patients with stage III non-small cell lung cancer (NSCLC). Although radiotherapy (RT) technologies have advanced dramatically, to the authors' knowledge relatively little known regarding importance of irradiation technique on outcome, particularly given competing risk distant metastasis. The National Cancer Data Base was used determine predictors overall survival (OS) in AJCC NSCLC who were treated chemoradiotherapy, focusing...

10.1002/cncr.28677 article EN Cancer 2014-04-01

First-line treatment for patients with non-small cell lung cancer (NSCLC) a sensitizing epidermal growth factor receptor (EGFR) mutation is tyrosine kinase inhibitor (TKI). Despite higher response rates and prolonged progression free survival (PFS) compared platinum doublet chemotherapy, subset of these do not receive benefit from agents. We investigate if the neutrophil-to-lymphocyte ratio (NLR) other markers cachexia chronic inflammation correlate worse outcomes in patients.This study...

10.3390/cancers13061426 article EN Cancers 2021-03-20
Alessio Cortellini Leonardo Brunetti Giuseppina Rita Di Fazio Edoardo Garbo David J. Pinato and 95 more Jarushka Naidoo Artur Katz Matthew J. Loza Joel W. Neal Carlo Genova Scott Gettinger So Yeon Kim Ritujith Jayakrishnan Talal El Zarif Marco Russano Federica Pecci Alessandro Di Federico Mark M. Awad Joao V. Alessi Michele Montrone Dwight H. Owen Diego Signorelli Mary J. Fidler Mingjia Li Andrea Camerini Andrea De Giglio Lauren Young Bruno Vincenzi Giulio Metro Francesco Passiglia Sai Yendamuri Annalisa Guida Michele Ghidini Nichola Awosika Andrea Napolitano Claudia A M Fulgenzi Salvatore Grisanti Francesco Grossi Armida D’Incecco Eleni Josephides Mieke Van Hemelrijck Alessandro Russo Alain Gelibter Gianpaolo Spinelli Monica Verrico Bartłomiej Tomasik Raffaele Giusti Thomas Newsom-Davis Emilio Bria Martin Sebastian Maximilian Rost Martin Förster Uma Mukherjee Lorenza Landi Francesca Mazzoni Avinash Aujayeb Madeleine Dupont Alessandra Curioni‐Fontecedro Rita Chiari Francesco Pantano Alessandro Morabito Alessandro Leonetti Alex Friedlaender Alfredo Addeo Federica Zoratto Michele De Tursi Luca Cantini Elisa Roca Giannis Mountzios Luigi Della Gravara Sukumar Kalvapudi Alessandro Inno Paolo Bironzo Rita Barros David O’Reilly Jack Bell Eleni Karapanagiotou Isabelle Monnet Javier Baena Preysler Marianna Macerelli Margarita Majem Francesco Agustoni Diego Cortinovis Giuseppe Tonini Gabriele Minuti Chiara Bennati Laura Mezquita Teresa Gorría Alberto Servetto Teresa Beninato Giuseppe Lo Russo Jacobo Rogado Laura Moliner Federica Biello Frank Aboubakar Nana Anne‐Marie C. Dingemans Joachim G.J.V. Aerts Roberto Ferrara Valter Torri Taher Abu Hejleh

Background Pembrolizumab monotherapy is an established front-line treatment for advanced non-small cell lung cancer (NSCLC) with programmed death-ligand 1 (PD-L1) tumor proportion score (TPS)≥50%. However, real-world data on its long-term efficacy remains sparse. Methods This study assessed 5-year outcomes of first-line pembrolizumab in a large, multicenter, cohort patients NSCLC and PD-L1 TPS≥50%, referred to as Pembro-real 5Y. Individual patient-level (IPD) from the experimental arm...

10.1136/jitc-2024-010674 article EN cc-by-nc-nd Journal for ImmunoTherapy of Cancer 2025-02-01

Abstract Approximately 30% of patients (pts) with non-small cell lung cancer (NSCLC) have alterations in the KRAS oncogene. In NSCLC mutational variants are diverse and therapeutically relevant. However, it is unclear how each variant associated tumor biology, including lipid metabolism immune microenvironment. Since perturbed infiltration linked to outcomes, we evaluated characterized association infiltration. Using Tempus Database, 5, 925 de-identified records from pts (G12A (n=464), G12C...

10.1158/1538-7445.am2025-2766 article EN Cancer Research 2025-04-21
Coming Soon ...