Matthew H. Taylor

ORCID: 0000-0003-2409-9001
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About
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Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Melanoma and MAPK Pathways
  • CAR-T cell therapy research
  • Lung Cancer Treatments and Mutations
  • Thyroid Cancer Diagnosis and Treatment
  • Colorectal Cancer Treatments and Studies
  • Immunotherapy and Immune Responses
  • Synthesis and biological activity
  • Lung Cancer Research Studies
  • Pancreatic and Hepatic Oncology Research
  • Colorectal and Anal Carcinomas
  • Head and Neck Cancer Studies
  • Bladder and Urothelial Cancer Treatments
  • Endometrial and Cervical Cancer Treatments
  • Cancer Genomics and Diagnostics
  • Advanced Breast Cancer Therapies
  • Virus-based gene therapy research
  • Renal cell carcinoma treatment
  • Salivary Gland Tumors Diagnosis and Treatment
  • Peptidase Inhibition and Analysis
  • Neuroendocrine Tumor Research Advances
  • Ovarian cancer diagnosis and treatment
  • Cancer Research and Treatments
  • Cancer-related Molecular Pathways
  • Radiomics and Machine Learning in Medical Imaging

Providence Portland Medical Center
2020-2025

University of Saskatchewan
2025

Pfizer (United States)
2025

Oregon Health & Science University
2015-2024

Providence College
2021-2023

University of the West Indies System
2023

HealthONE
2023

Cancer Institute (WIA)
2022

Angeles Clinic and Research Institute
2019

Cedars-Sinai Medical Center
2019

In a phase 1 dose-escalation study, combined inhibition of T-cell checkpoint pathways by nivolumab and ipilimumab was associated with high rate objective response, including complete responses, among patients advanced melanoma.

10.1056/nejmoa1414428 article EN New England Journal of Medicine 2015-04-20

Fusions involving one of three tropomyosin receptor kinases (TRK) occur in diverse cancers children and adults. We evaluated the efficacy safety larotrectinib, a highly selective TRK inhibitor, adults who had tumors with these fusions.We enrolled patients consecutively prospectively identified fusion-positive cancers, detected by molecular profiling as routinely performed at each site, into protocols: phase 1 study adults, 1-2 children, or 2 adolescents The primary end point for combined...

10.1056/nejmoa1714448 article EN New England Journal of Medicine 2018-02-21

Lenvatinib, an oral inhibitor of vascular endothelial growth factor receptors 1, 2, and 3, fibroblast 1 through 4, platelet-derived receptor α, RET, KIT, showed clinical activity in a phase 2 study involving patients with differentiated thyroid cancer that was refractory to radioiodine (iodine-131).In our randomized, double-blind, multicenter progressive iodine-131, we randomly assigned 261 receive lenvatinib (at daily dose 24 mg per day 28-day cycles) 131 placebo. At the time disease...

10.1056/nejmoa1406470 article EN New England Journal of Medicine 2015-02-11

Patients with advanced endometrial carcinoma have limited treatment options. We report final primary efficacy analysis results for a patient cohort receiving lenvatinib plus pembrolizumab in an ongoing phase Ib/II study of selected solid tumors.

10.1200/jco.19.02627 article EN cc-by-nc-nd Journal of Clinical Oncology 2020-03-13

Modulation of vascular endothelial growth factor-mediated immune suppression via angiogenesis inhibition may augment the activity checkpoint inhibitors. We report results from dose-finding and initial phase II expansion a Ib/II study lenvatinib plus pembrolizumab in patients with selected advanced solid tumors.Eligible had metastatic renal cell carcinoma (RCC), endometrial cancer, squamous head neck (SCCHN), melanoma, non-small-cell lung cancer (NSCLC), or urothelial cancer. The primary...

10.1200/jco.19.01598 article EN cc-by-nc-nd Journal of Clinical Oncology 2020-01-21

<h3>Importance</h3> Current treatment options for progressive ovarian cancer provide limited benefit, particularly in patients whose disease has become resistant to platinum-based chemotherapy. <h3>Objective</h3> To assess the efficacy and safety of avelumab, an anti–programmed death-ligand 1 agent, a cohort with previously treated recurrent or refractory cancer. <h3>Design, Setting, Participants</h3> In expansion phase 1b, open-label study (JAVELIN Solid Tumor), 125 advanced who had...

10.1001/jamaoncol.2018.6258 article EN JAMA Oncology 2019-01-25

The receptor tyrosine kinase rearranged during transfection (RET) is an oncogenic driver activated in multiple cancers, including non-small cell lung cancer (NSCLC), medullary thyroid (MTC), and papillary cancer. No approved therapies have been designed to target RET; treatment has limited multikinase inhibitors (MKI), which can significant off-target toxicities efficacy. BLU-667 a highly potent selective RET inhibitor overcome these limitations. In vitro, demonstrated ≥10-fold increased...

10.1158/2159-8290.cd-18-0338 article EN Cancer Discovery 2018-04-15

Nivolumab monotherapy is approved in the United States for third-line or later metastatic small cell lung cancer based on pooled data from nonrandomized and randomized cohorts of multicenter, open-label, phase 1/2 trial nivolumab ± ipilimumab (CheckMate 032; NCT01928394). We report updated results, including long-term overall survival (OS), cohort.Patients with disease progression after one to two prior chemotherapy regimens were 3:2 3 mg/kg every 2 weeks 1 plus four cycles followed by...

10.1016/j.jtho.2019.10.004 article EN cc-by-nc-nd Journal of Thoracic Oncology 2019-10-17

LBA9503 Background: mRNA-4157 is a novel mRNA-based personalized cancer vaccine which encodes up to 34 patient-specific tumor neoantigens. The open-label randomized Phase 2 mRNA-4157-P201/Keynote-942 trial met its primary endpoint of recurrence free survival (RFS) in patients with resected high-risk stage IIIB/C/D and IV melanoma. study has shown statistically significant clinically meaningful improvement RFS the combination therapy compared pembrolizumab monotherapy, reduction risk or death...

10.1200/jco.2023.41.17_suppl.lba9503 article EN Journal of Clinical Oncology 2023-06-07

<h3>Importance</h3> Patients with malignant mesothelioma whose disease has progressed after platinum and pemetrexed treatment have limited options. Anti–programmed cell death 1 (PD-1) antibodies antitumor activity in this disease, but little is known about the of anti–programmed ligand (PD-L1) patients mesothelioma. <h3>Objective</h3> To assess efficacy safety avelumab a cohort previously treated <h3>Design, Setting, Participants</h3> Phase 1b open-label study (JAVELIN Solid Tumor)...

10.1001/jamaoncol.2018.5428 article EN cc-by JAMA Oncology 2019-01-03

NTRK1, NTRK2 and NTRK3 gene fusions (NTRK fusions) occur in a range of adult cancers. Larotrectinib is potent highly selective ATP-competitive inhibitor TRK kinases has demonstrated activity patients with tumours harbouring NTRK fusions.

10.1093/annonc/mdy539 article EN cc-by-nc Annals of Oncology 2019-01-03

5533 Background: Avelumab* is a fully human anti-PD-L1 IgG1 antibody under clinical investigation in multiple cancers. We report safety and activity of avelumab patients (pts) with recurrent/refractory ovarian cancer (OC; NCT01772004). Methods: Pts advanced OC unselected for PD-L1 expression received 10 mg/kg IV Q2W until progression, unacceptable toxicity, or withdrawal. Tumors were assessed every 6 wks (RECIST 1.1). Unconfirmed objective response rate (ORR), progression-free survival...

10.1200/jco.2016.34.15_suppl.5533 article EN Journal of Clinical Oncology 2016-05-20

Purpose CD27, a costimulatory molecule on T cells, induces intracellular signals that mediate cellular activation, proliferation, effector function, and cell survival upon binding to its ligand, CD70. Varlilumab is novel, first-in-class, agonist CD27 antibody stimulates the pathway, which results in T-cell activation antitumor activity tumor models. This first-in-human, dose-escalation expansion study evaluated safety, pharmacology, of varlilumab patients with advanced solid tumors. Methods...

10.1200/jco.2016.70.1508 article EN Journal of Clinical Oncology 2017-05-02

5509 Background: The programmed death-1 receptor (PD-1) and its ligand (PD-L1) are key therapeutic targets in the reactivation of immune response against multiple cancers. Avelumab (proposed INN) (MSB0010718C) is a fully human anti-PD-L1 IgG1 antibody currently being investigated clinical trials. Here we present results from cohort patients (pts) with recurrent or refractory ovarian cancer an ongoing phase Ib study (NCT01772004). Methods: Pts ECOG PS 0-1 received avelumab at 10 mg/kg Q2W....

10.1200/jco.2015.33.15_suppl.5509 article EN Journal of Clinical Oncology 2015-05-20
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