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Daniel Rea
Researcher at University of Birmingham
Publications - 158
Citations - 7126
Daniel Rea is an academic researcher from University of Birmingham. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 40, co-authored 133 publications receiving 5726 citations. Previous affiliations of Daniel Rea include Churchill Hospital & Novartis.
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Journal ArticleDOI
Phase I Pharmacokinetic and Pharmacodynamic Study of the Oral Mammalian Target of Rapamycin Inhibitor Everolimus in Patients With Advanced Solid Tumors
Anne O'Donnell,Sandrine Faivre,Howard A. Burris,Daniel Rea,Vassiliki A. Papadimitrakopoulou,N. Shand,Heidi Lane,Katharine Hazell,Ulrike Zoellner,John M. Kovarik,Cathryn Brock,Suzanne F. Jones,Eric Raymond,Ian Judson +13 more
TL;DR: Everolimus was satisfactorily tolerated at dosages up to 70 mg/wk and 10 mg/d with predictable PK and Antitumor activity and PD in tumors require further clinical investigation.
Journal ArticleDOI
aTTom: Long-term effects of continuing adjuvant tamoxifen to 10 years versus stopping at 5 years in 6,953 women with early breast cancer.
Richard Gray,Daniel Rea,Kelly Handley,Sarah Bowden,P. Perry,H. M. Earl,Christopher J. Poole,T Bates,S Chetiyawardana,John Dewar,I. N. Fernando,R.J. Grieve,Jonathan Nicoll,Z Rayter,Anne Robinson,A. Salman,John Yarnold,S. Bathers,Andrea Marshall,M Lee,A C Grp +20 more
TL;DR: ATTom confirms that, in ER+ disease, continuing tamoxifen to year 10 rather than just to year 5 produces further reductions in recurrence, from year 7 onward, and breast cancer mortality after year 10.
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Antibacterial Prophylaxis after Chemotherapy for Solid Tumors and Lymphomas
Michael Cullen,Neil Steven,Lucinda Billingham,Claire Gaunt,Mark Hastings,Peter Simmonds,N. S. A. Stuart,Daniel Rea,Mark Bower,I. N. Fernando,Robert Huddart,Simon Gollins,Andrew Stanley +12 more
TL;DR: Among patients receiving chemotherapy for solid tumors or lymphoma, the prophylactic use of levofloxacin reduces the incidence of fever, probable infection, and hospitalization.
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Adjuvant tamoxifen and exemestane in early breast cancer (TEAM): a randomised phase 3 trial
Cornelis J.H. van de Velde,Daniel Rea,Caroline Seynaeve,Hein Putter,Annette Hasenburg,J.M. Vannetzel,Robert Paridaens,Christos Markopoulos,Yasuo Hozumi,E. T. M. Hille,Dirk G. Kieback,Lina Asmar,J. Smeets,Johan W.R. Nortier,Peyman Hadji,John M. S. Bartlett,Stephen E. Jones +16 more
TL;DR: In the safety analysis, sequential treatment was associated with a higher incidence of gynaecological symptoms and endometrial abnormalities than was exemestane alone, and treatment regimens of exemstane alone or after tamoxifen might be appropriate options for postmenopausal women with hormone-receptor-positive early breast cancer.
Journal ArticleDOI
Addressing overtreatment of screen detected DCIS; the LORIS trial
Adele Francis,Jeremy Thomas,Lesley Fallowfield,Matthew G. Wallis,John M. S. Bartlett,Cassandra Brookes,Tracy E Roberts,Sarah Pirrie,Claire Gaunt,Jennie Young,Lucinda Billingham,David Dodwell,Andrew M. Hanby,Sarah E Pinder,Andrew Evans,Malcolm W.R. Reed,Valerie Jenkins,L. Matthews,Maggie Wilcox,Patricia Fairbrother,Sarah Bowden,Daniel Rea +21 more
TL;DR: The background and development of 'The low risk' DCIS trial (LORIS), a phase III trial of surgery versus active monitoring, will determine if it is appropriate to manage women with screen detected or asymptomatic, low grade and intermediate grade DCIS with low grade features, by active monitoring rather than by surgical treatment.