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Donald C. McMillan

Researcher at Glasgow Royal Infirmary

Publications -  517
Citations -  32434

Donald C. McMillan is an academic researcher from Glasgow Royal Infirmary. The author has contributed to research in topics: Cancer & Colorectal cancer. The author has an hindex of 84, co-authored 469 publications receiving 26804 citations. Previous affiliations of Donald C. McMillan include NHS Greater Glasgow and Clyde & Gartnavel General Hospital.

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Cancer-related inflammation and treatment effectiveness

TL;DR: The complex interplay between local immune responses and systemic inflammation, and their influence on clinical outcomes, are examined, and potential anti-inflammatory interventions for patients with cancer are proposed.
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The systemic inflammation-based neutrophil–lymphocyte ratio: Experience in patients with cancer

TL;DR: The present systematic review examines and comments on the clinical utility of the neutrophil-lymphocyte ratio, which has shown that NLR is elevated in patients with more advanced or aggressive disease evidenced by increased tumour stage, nodal stage, number of metastatic lesions and as such these patients may represent a particularly high-risk patient population.
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The systemic inflammation-based Glasgow Prognostic Score: a decade of experience in patients with cancer.

TL;DR: The GPS/mGPS is the most extensively validated of the systemic inflammation-based prognostic scores and therefore may be used in the routine clinical assessment of patients with cancer and provides a well defined therapeutic target for future clinical trials.
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Role of systemic inflammatory response in predicting survival in patients with primary operable cancer

TL;DR: Good evidence is demonstrated that there is now good evidence that preoperative measures of the systemic inflammatory response predict cancer survival, independent of tumor stage, in primary operable cancer.
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Systemic inflammation, nutritional status and survival in patients with cancer.

TL;DR: Systemic inflammation-based prognostic scores not only identify patients at risk but also provide well defined therapeutic targets for future clinical trials targeting nutritional decline.