Tomislav Dragovich

ORCID: 0000-0002-1569-2172
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About
Contact & Profiles
Research Areas
  • Pancreatic and Hepatic Oncology Research
  • Colorectal Cancer Treatments and Studies
  • Cancer Genomics and Diagnostics
  • Cancer Immunotherapy and Biomarkers
  • Radiomics and Machine Learning in Medical Imaging
  • Neuroendocrine Tumor Research Advances
  • Cancer Treatment and Pharmacology
  • Glioma Diagnosis and Treatment
  • Lung Cancer Treatments and Mutations
  • Genetic factors in colorectal cancer
  • Cancer Research and Treatments
  • Gastric Cancer Management and Outcomes
  • Renal cell carcinoma treatment
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Click Chemistry and Applications
  • Advanced Breast Cancer Therapies
  • Esophageal Cancer Research and Treatment
  • Radiopharmaceutical Chemistry and Applications
  • Cancer therapeutics and mechanisms
  • Heat shock proteins research
  • Inflammatory mediators and NSAID effects
  • Cancer, Hypoxia, and Metabolism
  • Redox biology and oxidative stress
  • Neuroblastoma Research and Treatments
  • Lung Cancer Research Studies

Banner MD Anderson Cancer Center
2015-2024

The University of Texas MD Anderson Cancer Center
2015-2024

Banner Health
2012-2020

Brigham and Women's Hospital
2017

Dana-Farber Brigham Cancer Center
2017

Smilow Cancer Hospital
2017

Yale Cancer Center
2017

University of Arizona
2004-2014

Threshold Pharmaceuticals (United States)
2006-2014

University of Arizona Cancer Center
2007-2014

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

A phase II trial of the oral epidermal growth factor receptor (EGFR) inhibitor erlotinib in patients with gastroesophageal adenocarcinomas stratified according to primary tumor location into two groups: junction (GEJ)/cardia and distal gastric adenocarcinomas.Patients a histologically proven diagnosis adenocarcinoma GEJ or stomach (ST) that was unresectable metastatic; presence measurable disease; no prior chemotherapy for advanced metastatic cancer; Zubrod performance status (PS) 0 1;...

10.1200/jco.2006.07.1316 article EN Journal of Clinical Oncology 2006-10-18

PURPOSE Nivolumab received US Food and Drug Administration approval as a single agent or in combination with ipilimumab patients microsatellite instability-high/mismatch repair-deficient (MSI-H/dMMR) metastatic colorectal cancer (mCRC) that progressed following treatment fluoropyrimidine, oxaliplatin, irinotecan based on CheckMate 142. Presented are results of nivolumab plus low-dose the first-line therapy cohort from phase II 142 study. PATIENTS AND METHODS Patients no prior setting for...

10.1200/jco.21.01015 article EN Journal of Clinical Oncology 2021-10-12

TH-302 is an investigational hypoxia-activated prodrug that releases the DNA alkylator bromo-isophosphoramide mustard in hypoxic settings. This phase II study (NCT01144455) evaluated gemcitabine plus patients with previously untreated, locally advanced or metastatic pancreatic cancer.

10.1200/jco.2014.55.7504 article EN Journal of Clinical Oncology 2014-12-16

Purpose After curative resection of gastric or gastroesophageal junction adenocarcinoma, Intergroup Trial 0116 (Phase III trial postoperative adjuvant radiochemotherapy for high risk and adenocarcinoma: Demonstrated superior survival patients who received chemoradiotherapy with bolus fluorouracil (FU) leucovorin (LV) compared surgery alone. CALGB 80101 (Alliance; Phase Adjuvant Chemoradiation Resection Gastric Gastroesophageal Adenocarcinoma) assessed whether a regimen that replaced FU plus...

10.1200/jco.2017.74.2130 article EN Journal of Clinical Oncology 2017-10-04

Abstract Purpose: The purpose of the study was to evaluate stability phosphoprotein as a marker signaling activity in human tumors using clinical samples and xenografts. Experimental Design: expression phospho-Ser473-Akt (p-Akt) assessed by immunohistochemistry paraffin-embedded from patients enrolled Southwest Oncology Group trial gastroesophageal junction Western blotting colon tumor xenografts at various times after removal animal. Results: Clinical had evaluable p-Akt staining only when...

10.1158/1078-0432.ccr-05-0422 article EN Clinical Cancer Research 2005-06-15

4003 Background: Following curative resection of gastric or GEJ adenocarcinoma, INT-0116 demonstrated superior survival for pts who received postoperative bolus 5-FU and leucovorin (LV) before after concomitant RT compared to surgery alone. We assessed whether a chemoRT regimen that replaces 5-FU/LV with potentially more active systemic therapy (ECF) improves overall (OS). Methods: Patients resected adenocarcinoma were randomly assigned either: Arm A: 1 cycle 425 mg/m2/day plus LV20 5...

10.1200/jco.2011.29.15_suppl.4003 article EN Journal of Clinical Oncology 2011-05-20

11 Background: In the phase 2 CheckMate 142 trial, nivolumab plus low-dose ipilimumab provided robust and durable clinical benefit was well tolerated as first-line therapy for microsatellite instability-high/DNA mismatch repair deficient (MSI-H/dMMR) metastatic colorectal cancer (mCRC) (Lenz et al. Ann Oncol 2018;29:LBA18). Longer follow-up data will be presented. Methods: Patients with MSI-H/dMMR mCRC no prior treatment disease received 3 mg/kg every weeks 1 6 until progression or...

10.1200/jco.2020.38.4_suppl.11 article EN Journal of Clinical Oncology 2020-02-01

Abstract Purpose: Thioredoxin-1 (Trx-1) is a cellular redox protein that promotes tumor growth, inhibits apoptosis, and up-regulates hypoxia-inducible factor-1α vascular endothelial growth factor. Objectives of this study were to determine safety, tolerability, pharmacodynamics, pharmacokinetics PX-12, small-molecule inhibitor Trx-1. Experimental Design: Thirty-eight patients with advanced solid tumors received PX-12 at doses 9 300 mg/m2, as 1- or 3-h i.v. infusion on days 1 5, repeated...

10.1158/1078-0432.ccr-06-2250 article EN Clinical Cancer Research 2007-04-01

4040 Background: In the phase 2 CheckMate 142 trial, NIVO + low-dose IPI had robust, durable clinical benefit and was well tolerated as 1L therapy for MSI-H/dMMR mCRC (median follow-up 13.8 months [mo; range, 9–19]; Lenz et al. Ann Oncol 2018;29:LBA18). Longer is presented here. Methods: Patients (pts) with no prior treatment metastatic disease received 3 mg/kg Q2W 1 Q6W until progression or discontinuation. The primary endpoint investigator-assessed (INV) objective response rate (ORR) per...

10.1200/jco.2020.38.15_suppl.4040 article EN Journal of Clinical Oncology 2020-05-20

Background: In this international multicenter study, we aimed to determine the independent risk factors associated with increased 30 day mortality and impact of cancer novel treatment modalities in a large group patients without COVID-19 from multiple countries. Methods: We retrospectively collected de-identified data on cohort diagnosed between January November 2020 16 centers. Results: analyzed 3966 confirmed patients, 1115 2851 patients. Patients were more likely be pancytopenic have...

10.7554/elife.81127 article EN cc-by eLife 2023-01-30

Objectives: Cycloxygenase-2 (COX-2) is overexpressed in pancreatic tumors where it may be involved inflammation, carcinogenesis, and the regulation of neoangiogenesis. The purpose this trial was to evaluate combination intravenous gemcitabine with selective COX-2 inhibitor, celecoxib for effect on survival, disease progression, tolerability patients advanced cancer. In addition, limited pharmacokinetic pharmacodynamic analyses were preformed. Materials Methods: Eligible included those...

10.1097/coc.0b013e31815878c9 article EN American Journal of Clinical Oncology 2008-03-31

Abstract Purpose: The aim of the study was to determine safety, antitumor activity, and pharmacodynamic profile mogamulizumab, an anti-CCR4 monoclonal antibody targeting effector regulatory T cells (Treg) in combination with checkpoint inhibitor nivolumab patients locally advanced or metastatic solid tumors. Patients Methods: This a multicenter, dose-finding (phase I), dose expansion II) (NCT02705105) There were no dose-limiting toxicities phase I mogamulizumab 1 mg/kg every week for cycle...

10.1158/1078-0432.ccr-21-2781 article EN cc-by-nc-nd Clinical Cancer Research 2021-11-09

97 Background: NIVO + IPI demonstrated robust, durable clinical benefit and was well tolerated as a 1L therapy in pts with MSI-H/dMMR mCRC the phase 2 CheckMate 142 study (NCT02060188), leading to inclusion of NCCN guidelines an initial option for these pts. At 52-mo median follow-up, continued demonstrate benefit, no new safety signals were identified. Here we report longer follow-up results. Methods: Pts prior treatment metastatic disease received 3 mg/kg Q2W 1 Q6W until progression or...

10.1200/jco.2024.42.3_suppl.97 article EN Journal of Clinical Oncology 2024-01-20

Purpose Imexon, a pro-oxidant small molecule, has antitumor activity in preclinical models. The drug induces apoptosis through accumulation of reactive oxygen species. purpose this trial was to define the maximum-tolerated dose (MTD), toxicities, pharmacokinetics, and pharmacodynamics imexon patients with advanced cancers. Patients Methods Forty-nine metastatic cancer received intravenous over 30 45 minutes for 5 consecutive days (one course) every other week (days 1 15 19) monthly. Doses...

10.1200/jco.2006.08.9672 article EN Journal of Clinical Oncology 2007-04-30
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