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Mary J. Fidler

Researcher at Rush University Medical Center

Publications -  116
Citations -  7395

Mary J. Fidler is an academic researcher from Rush University Medical Center. The author has contributed to research in topics: Lung cancer & Cancer. The author has an hindex of 21, co-authored 95 publications receiving 5610 citations. Previous affiliations of Mary J. Fidler include Trinity School of Medicine.

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Pembrolizumab versus methotrexate, docetaxel, or cetuximab for recurrent or metastatic head-and-neck squamous cell carcinoma (KEYNOTE-040): a randomised, open-label, phase 3 study

Ezra E.W. Cohen, +107 more
- 12 Jan 2019 - 
TL;DR: The clinically meaningful prolongation of overall survival and favourable safety profile of pembrolizumab in patients with recurrent or metastatic head and neck squamous cell carcinoma support the further evaluation of p embrolizUMab as a monotherapy and as part of combination therapy in earlier stages of disease.
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Phase II Study of Maintenance Pembrolizumab in Patients with Extensive-Stage Small Cell Lung Cancer (SCLC)

TL;DR: Installing maintenance pembrolizumab in patients with extensive‐stage SCLC after treatment with platinum and etoposide did not appear to improve median PFS compared with the historical data, however, the 1‐year PFS rate of 13% and OS rate of 37% suggest that a subset of patients did benefit from pembrolexumab.
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Intratumoral injection of the seasonal flu shot converts immunologically cold tumors to hot and serves as an immunotherapy for cancer

TL;DR: It is reported that unadjuvanted seasonal influenza vaccination via intratumoral, but not intramuscular, injection converts “cold” tumors to hot, generates systemic CD8+ T cell-mediated antitumor immunity, and sensitizes resistant tumors to checkpoint blockade, and proposes that antipathogen vaccines may be utilized for both infection prevention and repurposing as a cancer immunotherapy.
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Esophageal carcinoma advances in treatment results for locally advanced disease: review

TL;DR: Chemo (PF) before surgery improved overall survival (OS) in those patients in most of the randomized trials and in meta-analyses and it was found that those patients with pathologic complete response to the initial treatment did better than those who had no improvement at all.