Imperial College London

DrSarahBlagden

Faculty of MedicineDepartment of Surgery & Cancer

Honorary Clinical Senior Lecturer
 
 
 
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Contact

 

s.blagden

 
 
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Location

 

Cyclotron buildingHammersmith Campus

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Summary

 

Publications

Publication Type
Year
to

74 results found

Vidal L, Blagden S, Attard G, de Bono Jet al., 2005, Making sense of antisense, EUROPEAN JOURNAL OF CANCER, Vol: 41, Pages: 2812-2818, ISSN: 0959-8049

Journal article

Steele N, Vidal L, Plumb J, Attard G, Rasmussen A, Buhl-Jensen P, Brown R, Blagden S, Evans J, de Bono Jet al., 2005, A phase 1 pharmacokinetic (PK) and pharmacodynamic (PD) study of the histone deacetylase (HDAC) inhibitor PXD101 in patients (pts) with advanced solid tumours., 41st Annual Meeting of the American-Society-of-Clinical-Oncology, Publisher: AMER SOC CLINICAL ONCOLOGY, Pages: 200S-200S, ISSN: 0732-183X

Conference paper

Pacey S, Plummer RE, Attard G, Bale C, Calvert AH, Blagden S, Fox NL, Corey A, de Bono JSet al., 2005, Phase I and pharmacokinetic study of HGS-ETR2, a human monoclonal antibody to TRAIL R2, in patients with advanced solid malignancies., 41st Annual Meeting of the American-Society-of-Clinical-Oncology, Publisher: AMER SOC CLINICAL ONCOLOGY, Pages: 205S-205S, ISSN: 0732-183X

Conference paper

Blagden S, Thomas A, De-Bono JS, Ahmed S, Greystoke A, Attard G, Jenner A, Fong P, Steward WPet al., 2005, Phase I study of intravenous TZT-1027 (T) and carboplatin (C), administered on Day 1 (T and C) and Day 8 (T) every three weeks in patients (pts) with advanced solid tumors, 41st Annual Meeting of the American-Society-of-Clinical-Oncology, Publisher: AMER SOC CLINICAL ONCOLOGY, Pages: 226S-226S, ISSN: 0732-183X

Conference paper

Attard G, Kitzen JJ, de Bono J, Verweij J, Pronk L, Zhi J, Blagden SP, Reade SE, Zugmaier G, de Jonge MJet al., 2005, A phase 1b study of pertuzumab (P), a recombinant humanized antibody to HER2, and docetaxel (D) in patients (pts) with advanced solid tumors, 41st Annual Meeting of the American-Society-of-Clinical-Oncology, Publisher: AMER SOC CLINICAL ONCOLOGY, Pages: 232S-232S, ISSN: 0732-183X

Conference paper

Blagden S, de Bono J, 2005, Drugging cell cycle kinases in cancer therapy, CURRENT DRUG TARGETS, Vol: 6, Pages: 325-335, ISSN: 1389-4501

Journal article

Blagden SP, Kaye SB, 2005, Docetaxel in the management of ovarian cancer, EXPERT REVIEW OF ANTICANCER THERAPY, Vol: 5, Pages: 203-214, ISSN: 1473-7140

Journal article

Blagden SP, Charman SC, Sharples LD, Magee LRA, Gilligan Det al., 2003, Performance status score: do patients and their oncologists agree?, BRITISH JOURNAL OF CANCER, Vol: 89, Pages: 1022-1027, ISSN: 0007-0920

Journal article

Blagden SP, Glover DM, 2003, Polar expeditions - provisioning the centrosome for mitosis, NATURE CELL BIOLOGY, Vol: 5, Pages: 505-511, ISSN: 1465-7392

Journal article

Blagden SP, Foskett MA, Fisher RA, Short D, Fuller S, Newlands ES, Seckl MJet al., 2002, The effect of early pregnancy following chemotherapy on disease relapse and foetal outcome in women treated for gestational trophoblastic tumours, BRITISH JOURNAL OF CANCER, Vol: 86, Pages: 26-30, ISSN: 0007-0920

Journal article

Corrie P, Mayer A, Shaw J, D'Ath S, Blagden S, Blesing C, Price P, Warner Net al., 2002, Phase II study to evaluate combining gemcitabine with flutamide in advanced pancreatic cancer patients, Br J Cancer, Vol: 87, Pages: 716-719

A phase II study was undertaken to determine the safety of combining flutamide with gemcitabine, with response rate being the primary end point. Twenty-seven patients with histologically proven, previously untreated, unresectable pancreatic adenocarcinoma received gemcitabine, 1 g m(-2) intravenously on days 1, 8 and 15 of a 28 day cycle, and flutamide 250 mg given orally three times daily. Treatment was halted if there was unacceptable toxicity, or evidence of disease progression. Toxicity was documented every cycle. Tumour assessment was undertaken after cycles 2 and 4, and thereafter at least every additional four cycles. One hundred and seventeen cycles of treatment were administered, median four cycles per patient (range 1-18). Gemcitabine combined with flutamide was well tolerated, with most toxicities being recorded as grade 1 or 2 and only nine treatment cycles associated with grade 3 toxicity. The most frequent toxicity was myelosuppression. One case of transient jaundice was recorded. The commonest symptomatic toxicity was nausea and vomiting. The response rate was 15% (four partial responses), median survival 6 months and 22% of patients were alive at 1 year. These results suggest antitumour activity of the combination therapy to be equivalent to single agent gemcitabine. doi:10.1038/sj.bjc.6600523 www.bjcancer.comCopyright 2002 Cancer Research UK

Journal article

Seckl MJ, Blagden SP, Foskett MA, Fuller S, Short D, Newlands ESet al., 1999, Outcome in patients who become pregnant within 12 months after completing single and multiple agent chemotherapy for gestational trophoblastic disease (GTD), EUROPEAN JOURNAL OF CANCER, Vol: 35, Pages: S231-S231, ISSN: 0959-8049

Journal article

Blagden SP, Earl HM, Brenton J, Murray N, Shaw CJet al., 1999, A study of epirubicin, cisplatin and prolonged infusional 5-FU (ECF) treatment for relapsed epithelial ovarian cancer, BRITISH JOURNAL OF CANCER, Vol: 80, Pages: 107-107, ISSN: 0007-0920

Journal article

Lo SK, Montgomery JN, Blagden S, McNeish IA, Agarwal R, Suntharalingam J, Seckl MJ, Newlands ESet al., 1999, Reducing incidence of headache after lumbar puncture and intrathecal cytotoxics, LANCET, Vol: 353, Pages: 2038-2039, ISSN: 0140-6736

Journal article

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