Bevacizumab with peri-operative epirubicin, cisplatin and capecitabine (ECX) in localised gastro-oesophageal adenocarcinoma: a safety report

被引:60
作者
Okines, A. F. C. [1 ]
Langley, R. E. [2 ]
Thompson, L. C. [2 ]
Stenning, S. P. [2 ]
Stevenson, L. [2 ]
Falk, S. [3 ]
Seymour, M. [4 ]
Coxon, F. [5 ]
Middleton, G. W. [6 ]
Smith, D. [7 ]
Evans, L. [8 ]
Slater, S. [9 ]
Waters, J. [10 ]
Ford, D. [11 ]
Hall, M. [12 ]
Iveson, T. J. [13 ]
Petty, R. D. [14 ]
Plummer, C. [5 ]
Allum, W. H. [1 ]
Blazeby, J. M. [15 ]
Griffin, M. [16 ]
Cunningham, D. [1 ]
机构
[1] Royal Marsden Hosp NHS Fdn Trust London & Surrey, Dept Med, London, England
[2] MRC, Clin Trials Unit, London, England
[3] Bristol Haematol & Oncol Ctr, Bristol, Avon, England
[4] Univ Leeds, St Jamess Hosp, Leeds, W Yorkshire, England
[5] Freeman Rd Hosp, Dept Med Oncol, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
[6] Royal Surrey Cty Hosp, Dept Med Oncol, Guildford, Surrey, England
[7] Clatterbridge Canc Ctr NHS Fdn Trust, Dept Oncol, Clatterbridge, Merseyside, England
[8] Weston Pk Hosp, Dept Med Oncol, Sheffield, S Yorkshire, England
[9] St Barts Hosp, Dept Oncol, London, England
[10] Maidstone Hlth Author, Kent Oncol Ctr, Maidstone, Kent, England
[11] Queen Elizabeth Hosp, Dept Oncol, Birmingham B15 2TH, W Midlands, England
[12] Wexham Pk Hosp, Dept Med Oncol, Northwood, Middx, England
[13] Univ Southampton, Sch Med, Canc Res UK Clin Ctr, Southampton, Hants, England
[14] Aberdeen Royal Infirm, Dept Oncol, Aberdeen, Scotland
[15] Univ Bristol, Dept Surg, Bristol, Avon, England
[16] Royal Victoria Infirm, Dept Surg, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
关键词
adenocarcinoma; bevacizumab; chemotherapy; gastric; oesophagus; peri-operative; METASTATIC COLORECTAL-CANCER; ANGIOGENESIS INHIBITOR BEVACIZUMAB; 1ST-LINE THERAPY; PHASE-II; CHEMOTHERAPY; COMBINATION; OXALIPLATIN; THROMBOEMBOLISM; FLUOROURACIL; LEUCOVORIN;
D O I
10.1093/annonc/mds533
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Pen-operative chemotherapy and surgery is a standard treatment of localised oesophagogastric adenocarcinoma; however, the outcomes remain poor. Patients and methods: ST03 is a multicentre, randomised, phase II/III study comparing pen-operative ECX with or without bevacizumab (ECX-B). The primary outcome measure of phase II (n = 200) was safety, specifically gastrointestinal (GI) perforation rates and cardiotoxicity. Results: Two hundred patients were randomised between October 2007 and April 2010. Ninety-one/101 (90%) ECX and 86/99 (87%) ECX-B patients completed pre-operative chemotherapy; 7 ECX and 9 ECX-B patients stopped due to toxicity. Gastrointestinal perforations (3 ECX, 1 ECX-B), cardiac events (1 ECX, 4 ECX-B) and venous thromboembolic events (VEs, 8 ECX, 7 ECX-B) were uncommon. Arterial thromboembolic events (ATEs, myocardial infarction (MI) or cerebrovascular accident) were more frequent with ECX-B (5 versus 1 with ECx). Delayed wound healing, anastomotic leaks and GI bleeding rates were similar.More asymptomatic left ventricular ejection fraction (LVEF) falls (>= 15% and/or to <50%) occurred with ECX-B (21.2% versus 11.1% with ECX). Clinically significant falls (>= 10% to below lower limit of normal, LLN) occurred in (15.3%) and (8.9%) respectively, with no associated cardiac failure (median 22 months follow-up). Conclusions: Addition of bevacizumab to pen-operative ECX chemotherapy is feasible with acceptable toxicity and no negative impact on surgical outcomes.
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收藏
页码:702 / 709
页数:8
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