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William J. John

Researcher at University of Kentucky

Publications -  22
Citations -  1354

William J. John is an academic researcher from University of Kentucky. The author has contributed to research in topics: Gemcitabine & Radiation therapy. The author has an hindex of 11, co-authored 22 publications receiving 1288 citations. Previous affiliations of William J. John include Eli Lilly and Company.

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PARAMOUNT: Final Overall Survival Results of the Phase III Study of Maintenance Pemetrexed Versus Placebo Immediately After Induction Treatment With Pemetrexed Plus Cisplatin for Advanced Nonsquamous Non–Small-Cell Lung Cancer

TL;DR: Pemetrexed continuation maintenance therapy is well-tolerated and offers superior OS compared with placebo, further demonstrating that it is an efficacious treatment strategy for patients with advanced nonsquamous NSCLC and good performance status who did not progress during pemetrexing-cisplatin induction therapy.
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Immune Response to the Carcinoembryonic Antigen in Patients Treated with an Anti-Idiotype Antibody Vaccine

TL;DR: This is the first report demonstrating that a vaccine therapy is capable of breaking "immune tolerance" to CEA in patients with CEA positive tumors.
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Preoperative chemoradiation in fixed distal rectal cancer: dose time factors for pathological complete response.

TL;DR: Dose intensity of 5-FU and dose of radiation correlate significantly with the likelihood of achieving a pCR, and a preoperative radiation dose of 5500 cGy or higher can achieve pCR rates of approximately 50%, even in fixed cancers of the rectum.
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Clinical and Immune Responses in Resected Colon Cancer Patients Treated With Anti-Idiotype Monoclonal Antibody Vaccine That Mimics the Carcinoembryonic Antigen

TL;DR: CeaVac consistently generated a potent anti-CEA humoral and cellular immune response in all 32 patients entered onto this trial, and these data warrant a phase III trial for patients with resected colon cancer.
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Resting energy expenditure in patients with alcoholic hepatitis.

TL;DR: The measured energy expenditure per gram of creatinine was significantly increased in alcoholic hepatitis patients, supporting the concept of alcoholic hepatitis as a hypermetabolic state.