Daniel W. Bowles

ORCID: 0000-0003-1406-0963
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About
Contact & Profiles
Research Areas
  • Thyroid Cancer Diagnosis and Treatment
  • Salivary Gland Tumors Diagnosis and Treatment
  • Lung Cancer Treatments and Mutations
  • Colorectal Cancer Treatments and Studies
  • Head and Neck Cancer Studies
  • Melanoma and MAPK Pathways
  • Synthesis and biological activity
  • Tumors and Oncological Cases
  • Cancer, Hypoxia, and Metabolism
  • S100 Proteins and Annexins
  • PI3K/AKT/mTOR signaling in cancer
  • Hedgehog Signaling Pathway Studies
  • Chronic Lymphocytic Leukemia Research
  • Ear and Head Tumors
  • Cancer-related Molecular Pathways
  • Cancer Cells and Metastasis
  • Biochemical and Molecular Research
  • Oral and Maxillofacial Pathology
  • COVID-19 and healthcare impacts
  • BRCA gene mutations in cancer
  • Cancer Diagnosis and Treatment
  • Lung Cancer Research Studies
  • Cancer-related gene regulation
  • Nutrition, Genetics, and Disease
  • Bladder and Urothelial Cancer Treatments

University of Colorado Anschutz Medical Campus
2017-2024

University of Colorado Denver
2015-2024

University of Colorado Cancer Center
2012-2024

University of Colorado Hospital
2023-2024

University of Colorado Health
2023

Dana-Farber Cancer Institute
2023

National Cancer Center
2023

Michigan United
2023

University of California, Los Angeles
2023

Seoul National University Hospital
2023

Nicole M. Kuderer Toni K. Choueiri Dimpy P. Shah Yu Shyr Samuel M. Rubinstein and 95 more Donna R. Rivera Sanjay Shete Chih–Yuan Hsu Aakash Desai Gilberto Lopes Petros Grivas Corrie Painter Solange Peters Michael A. Thompson Ziad Bakouny Gerald Batist Tanios Bekaii‐Saab Mehmet Asım Bilen Nathaniel Bouganim Mateo Bover Larroya Daniel Castellano Salvatore A. Del Prete Deborah B. Doroshow Pamela Egan Arielle Elkrief Dimitrios Farmakiotis Daniel Flora Matthew D. Galsky Michael Glover Elizabeth A. Griffiths Anthony P. Gulati Shilpa Gupta Navid Hafez Þorvarður R. Hálfdánarson Jessica E. Hawley Emily Hsu Anup Kasi Ali Raza Khaki Christopher A. Lemmon Colleen Lewis Barbara Logan Tyler Masters Rana R. McKay Ruben A. Mesa Alicia K. Morgans Mary F. Mulcahy Orestis A. Panagiotou Prakash Peddi Nathan A. Pennell Kerry L. Reynolds L Rosen Rachel Rosovsky Mary Salazar Andrew Schmidt Sumit Shah Justin Shaya John A. Steinharter Keith Stockerl‐Goldstein Suki Subbiah Donald C. Vinh Firas Wehbe Lisa B. Weissmann Julie Wu Elizabeth Wulff‐Burchfield Zhuoer Xie Albert C. Yeh Peter Paul Yu Alice Y. Zhou Leyre Zubiri Sanjay Mishra Gary H. Lyman Brian I. Rini Jeremy L. Warner Maheen Z. Abidi Jared D. Acoba Neeraj Agarwal Syed A. Ahmad Archana Ajmera Jessica K. Altman Anne H. Angevine Nilo Azad Michael Bär Aditya Bardia Jill S. Barnholtz‐Sloan Briana Barrow Babar Bashir Rimma Belenkaya Stephanie Berg Eric Bernicker Christine M. Bestvina Rohit Bishnoi Genevieve M. Boland Mark Bonnen Gabrielle Bouchard Daniel W. Bowles Fiona Busser Angelo Cabal Paolo F. Caimi Theresa M. Carducci Carla Casulo

10.1016/s0140-6736(20)31187-9 article EN other-oa The Lancet 2020-05-28

Abstract Purpose: To define the genetic landscape of advanced differentiated and anaplastic thyroid cancer (ATC) identify alterations potential diagnostic, prognostic, therapeutic significance. Experimental Design: The profiles 583 196 ATCs generated with targeted next-generation sequencing cancer-associated gene panels MSK-IMPACT FoundationOne were analyzed. Results: ATC had more per tumor, pediatric papillary fewer tumor when compared other types. DNA mismatch repair deficit activity...

10.1158/1078-0432.ccr-18-0373 article EN Clinical Cancer Research 2018-04-03
Petros Grivas Ali Raza Khaki Trisha M. Wise‐Draper Benjamin French Conor Hennessy and 95 more Chih–Yuan Hsu Yu Shyr Xuanyi Li Toni K. Choueiri Corrie Painter Solange Peters Brian I. Rini Michael A. Thompson Sanjay Mishra Donna R. Rivera Jared D. Acoba Maheen Z. Abidi Ziad Bakouny Babar Bashir Tanios Bekaii‐Saab Stephanie Berg Eric Bernicker Mehmet Asım Bilen Poorva Bindal Rohit Bishnoi Nathaniel Bouganim Daniel W. Bowles Angelo Cabal Paolo F. Caimi David D. Chism Jennifer Crowell Catherine Curran Aakash Desai Becky Dixon Deborah B. Doroshow Eric B. Durbin Arielle Elkrief Dimitrios Farmakiotis Aldo Di Fazio Leslie A. Fecher D. Flora Christopher R. Friese Julie Fu Shirish M. Gadgeel Matthew D. Galsky David Gill Michael Glover Sharad Goyal Punita Grover Shuchi Gulati Shilpa Gupta Susan Halabi Þorvarður R. Hálfdánarson Balázs Halmos Daniel Hausrath Jessica E. Hawley Emily Hsu Minh‐Phuong Huynh‐Le Clara Hwang Chinmay Jani Asha Jayaraj Douglas B. Johnson Anup Kasi H. Khan Vadim S. Koshkin Nicole M. Kuderer Daniel H. Kwon Philip E. Lammers A. Li Arturo Loaiza‐Bonilla Clarke A. Low Maryam B. Lustberg Gary H. Lyman Rana R. McKay Christopher McNair H. Menon Ruben A. Mesa Vasil Mico Daniel Mundt Gayathri Nagaraj Elizabeth S. Nakasone John Nakayama Amanda Nizam Nora L. Nock C. Park Jaymin Patel Kanishka G. Patel Prakash Peddi Nathan A. Pennell Andrew J. Piper‐Vallillo Matthew Puc Deepak Ravindranathan Mark E. Reeves Daniel Y. Reuben Lori J. Rosenstein Rachel Rosovsky Samuel M. Rubinstein M. Salazar Andrew Schmidt Gary K. Schwartz

Patients with cancer may be at high risk of adverse outcomes from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We analyzed a cohort patients and 2019 (COVID-19) reported to the COVID-19 Cancer Consortium (CCC19) identify prognostic clinical factors, including laboratory measurements anticancer therapies. active or historical laboratory-confirmed SARS-CoV-2 diagnosis recorded between 17 March 18 November 2020 were included. The primary outcome was severity measured...

10.1016/j.annonc.2021.02.024 article EN cc-by Annals of Oncology 2021-03-20

Abstract Oncogenic RET fusions occur in diverse cancers. Pralsetinib is a potent, selective inhibitor of receptor tyrosine kinase. ARROW ( NCT03037385 , ongoing) was designed to evaluate pralsetinib efficacy and safety patients with advanced -altered solid tumors. Twenty-nine 12 different fusion–positive tumor types, excluding non-small-cell lung cancer thyroid cancer, who had previously received or were not candidates for standard therapies, enrolled. The most common fusion partners 23...

10.1038/s41591-022-01931-y article EN cc-by Nature Medicine 2022-08-01

RET fusions are present in 1%-2% of non-small-cell lung cancer (NSCLC). Pralsetinib, a highly potent, oral, central nervous system-penetrant, selective inhibitor, previously demonstrated clinical activity patients with fusion-positive NSCLC the phase I/II ARROW study, including among treatment-naive patients. We report an updated analysis from study.ARROW is multi-cohort, open-label, study. Eligible were ≥18 years age locally advanced or metastatic solid tumours and Eastern Cooperative...

10.1016/j.annonc.2022.08.002 article EN cc-by-nc-nd Annals of Oncology 2022-08-13

Abstract Purpose: The objectives of the study were to evaluate maximum tolerated dose (MTD), safety, pharmacodynamics, pharmacokinetics, and antitumor activity PX-866 in patients with incurable cancers. Experimental Design: This was a phase I, open-label, dose-escalation study. Drug administered orally once per day either on an intermittent (arm 1; days 1–5 8–12 28-day cycle) or continuous 2; 1–28 schedule. Additional treated at arm 2 MTD food effects substudy. Results: Eighty-four 1 (n =...

10.1158/1078-0432.ccr-12-0714 article EN Clinical Cancer Research 2012-06-13

<h3>Importance</h3> Data on adjuvant concurrent chemoradiotherapy (CRT) after resection of salivary gland carcinomas (SGCs) are limited. <h3>Objective</h3> To examine overall survival (OS) outcomes patients who receive CRT vs radiotherapy (RT) alone SGCs. <h3>Design, Setting, and Participants</h3> The National Cancer Base (NCDB), a hospital-based registry that represents 70% all cancer cases in the United States, was queried for underwent major SGCs with at least 1 high-risk feature (T3-T4...

10.1001/jamaoto.2016.2168 article EN JAMA Otolaryngology–Head & Neck Surgery 2016-08-19

We sought to identify genomic alterations (GA) in salivary gland adenocarcinomas, not otherwise specified (NOS), duct carcinomas (SDC), carcinoma ex pleomorphic adenoma (ca PA), and carcinoma, NOS.DNA was extracted from 149 tumors. Comprehensive profiling (CGP) performed on hybridization-captured adaptor ligation-based libraries of 182 or 315 cancer-related genes plus introns 14 28 frequently rearranged for cancer evaluated all classes GAs.A total 590 GAs were found 157 unique (mean...

10.1158/1078-0432.ccr-15-2568 article EN Clinical Cancer Research 2016-06-23

•Pertuzumab + trastuzumab produced a response in 60% (9/15) of patients with HER2-amplified/overexpressing salivary cancer.•Stable disease was observed patient HER2-mutated cancer treated pertuzumab trastuzumab.•Vismodegib, vemurafenib, and atezolizumab responses tumors matched genomic alterations.•Safety for each treatment consistent previously reported safety profiles.•Results support use molecular profiling to identify effective chemotherapy-free targeted treatments cancers....

10.1016/j.annonc.2019.11.018 article EN cc-by-nc-nd Annals of Oncology 2020-01-06

Immunotherapy for recurrent and/or metastatic (R/M) squamous cell carcinoma of the head and neck (SCCHN) is promising. The toll-like receptor 8 (TLR8) agonist motolimod may stimulate innate adaptive immunity.To determine whether improves outcomes R/M SCCHN when combined with standard therapy.The Active8 study was a multicenter, randomized, double-blind, placebo-controlled clinical trial enrolling adult patients (age ≥18 years) histologically confirmed oral cavity, oropharynx, hypopharynx, or...

10.1001/jamaoncol.2018.1888 article EN JAMA Oncology 2018-06-21

Relapsed/metastatic salivary gland carcinomas (SGCs) have a wide diversity of histologic subtypes associated with variable clinical aggressiveness and response to local systemic therapies. We queried whether comprehensive genomic profiling could define the tumor uncover clinically relevant alterations, revealing new routes targeted therapies for patients relapsed metastatic disease.From series 85 686 cases, DNA was extracted from 40 µm formalin-fixed paraffin embedded (FFPE) sections 623...

10.1093/annonc/mdx399 article EN cc-by-nc Annals of Oncology 2017-08-03

The overall survival (OS) benefit of concurrent chemoradiotherapy (CRT) for head and neck squamous cell carcinoma patients older than 70 years is debated. This study examines the outcomes elderly receiving CRT versus radiotherapy (RT) alone.The National Cancer Data Base was queried with nonmetastatic oropharyngeal, laryngeal, or hypopharyngeal cancer (T3-4 N(+)). defined as chemotherapy started within 14 days initiation RT. Univariate analysis, multivariate analysis (MVA), propensity score...

10.1002/cncr.29956 article EN Cancer 2016-03-11

Abstract Five-year survival for human papilloma virus-unrelated head and neck squamous cell carcinomas remain below 50%. We assessed the safety of administering combination hypofractionated stereotactic body radiation therapy with single-dose durvalumab (anti-PD-L1) neoadjuvantly ( n = 21) NCT03635164 ). The primary endpoint study was safety, which met. Secondary endpoints included radiographic, pathologic objective response; locoregional control; progression-free survival; overall survival....

10.1038/s43018-022-00450-6 article EN cc-by Nature Cancer 2022-11-25

PURPOSE Radiotherapy (RT)/cetuximab (C) demonstrated superiority over RT alone for locally advanced squamous head and neck cancer. We tested this in completely resected, intermediate-risk METHODS Patients had cell carcinoma of the (SCCHN) oral cavity, oropharynx, or larynx, with one more risk factors warranting postoperative RT. were randomly assigned 1:1 to intensity-modulated (60-66 Gy) once-per-week C alone. The primary hypothesis was that + would improve overall survival (OS)...

10.1200/jco-24-01829 article EN Journal of Clinical Oncology 2025-01-22
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