S. Gwynne

ORCID: 0000-0001-7750-5320
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About
Contact & Profiles
Research Areas
  • Esophageal Cancer Research and Treatment
  • Lung Cancer Diagnosis and Treatment
  • Gastric Cancer Management and Outcomes
  • Advanced Radiotherapy Techniques
  • Radiomics and Machine Learning in Medical Imaging
  • Medical Imaging Techniques and Applications
  • Colorectal and Anal Carcinomas
  • Colorectal Cancer Surgical Treatments
  • Esophageal and GI Pathology
  • Cancer Immunotherapy and Biomarkers
  • Neuroendocrine Tumor Research Advances
  • Lung Cancer Treatments and Mutations
  • Advances in Oncology and Radiotherapy
  • Immunotherapy and Immune Responses
  • Cutaneous Melanoma Detection and Management
  • Pancreatic and Hepatic Oncology Research
  • Immune Cell Function and Interaction
  • Cancer Genomics and Diagnostics
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Health Systems, Economic Evaluations, Quality of Life
  • Radiopharmaceutical Chemistry and Applications
  • Melanoma and MAPK Pathways
  • Radiation Therapy and Dosimetry
  • Intraperitoneal and Appendiceal Malignancies
  • CAR-T cell therapy research

Singleton Hospital
2015-2024

Swansea University
2019-2024

Swansea Bay University Health Board
2015-2024

Velindre Cancer Centre
2008-2020

Mount Vernon Hospital
2019

Beatson West of Scotland Cancer Centre
2016-2018

Cardiff University
2014-2017

University of Wales Institute Cardiff
2015-2017

Institute of Infection and Immunity
2017

Oxford BioMedica (United Kingdom)
2017

Abstract Purpose: Anticancer T-cell responses can control tumors, but immunosuppressive mechanisms in vivo prevent their function. The role of regulatory T cells (Tregs) metastatic colorectal cancer is unclear. We have previously shown depletion Tregs enhances cancer–specific effector responses. Low-dose cyclophosphamide targets animal models and some human studies; however, the effect unknown. Experimental Design: Fifty-five patients with were enrolled a phase I/II trial randomly assigned...

10.1158/1078-0432.ccr-17-0895 article EN Clinical Cancer Research 2017-08-30

The success of immunotherapy with checkpoint inhibitors is not replicated in most cases colorectal cancer; therefore, different strategies are urgently required. oncofetal antigen 5T4 expressed more than 90% metastatic cancer (mCRC). Preliminary data using modified vaccinia Ankara-5T4 (MVA-5T4) mCRC demonstrated that it safely induced serologic and T-cell responses.

10.1001/jamaoncol.2017.2579 article EN JAMA Oncology 2017-09-07

Pelvic exenteration is a potentially curative treatment for locally advanced primary rectal cancer. Previous studies have been limited by small sample sizes and heterogeneous data. A consecutive series of patients was studied to identify the clinicopathological determinants survival.All undergoing pelvic exenterative surgery cancer (1992-2014) at this hospital were analysed. The outcome measure 5-year overall survival. Secondary endpoints included length stay, complication rate, 30-day...

10.1002/bjs.9841 article EN British journal of surgery 2015-06-11

Abstract Background This study compared outcomes after surgery alone for stage II/ III rectal cancer in a tertiary unit versus highly selective use of preoperative chemoradiotherapy (CRT). Methods was single-centre retrospective cohort consecutive patients receiving potentially curative II and primary cancer. CRT given only magnetic resonance imaging-predicted circumferential resection margin (CRM) involvement nodal disease (at least N2). Primary endpoints were CRM local recurrence rates....

10.1002/bjs.9570 article EN British journal of surgery 2014-06-12

Both oxaliplatin/capecitabine-based chemoradiation (OXCAP-RT) and carboplatin-paclitaxel based radiation (CarPac-RT) are active regimens in oesophageal adenocarcinoma, but no randomised study has compared their efficacy toxicity. This phase II “pick a winner” trial will identify the optimum regimen to take forward future III against neo-adjuvant chemotherapy, current standard UK. Patients with resectable adenocarcinoma of oesophagus or Siewert Type 1–2 gastro-oesophageal junction (GOJ), ≥T3...

10.1186/s12885-015-1062-y article EN cc-by BMC Cancer 2015-02-11
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