Impact of perioperative chemotherapy on oncological outcomes after gastric cancer surgery

被引:27
作者
Bringeland, E. A. [1 ]
Wasmuth, H. H. [1 ]
Fougner, R. [2 ]
Mjones, P. [3 ]
Gronbech, J. E. [1 ,4 ]
机构
[1] Univ Trondheim Hosp, St Olavs Hosp, Dept Gastrointestinal Surg, N-7006 Trondheim, Norway
[2] Univ Trondheim Hosp, St Olavs Hosp, Dept Radiol, N-7006 Trondheim, Norway
[3] Univ Trondheim Hosp, St Olavs Hosp, Dept Pathol, N-7006 Trondheim, Norway
[4] Norwegian Univ Sci & Technol, Dept Canc Res & Mol Med, N-7034 Trondheim, Norway
关键词
NEOADJUVANT CHEMOTHERAPY; ADENOCARCINOMA; TRIAL; STOMACH;
D O I
10.1002/bjs.9650
中图分类号
R61 [外科手术学];
学科分类号
摘要
BackgroundPerioperative chemotherapy has become standard care for resectable gastric cancer. However, available evidence is based on a limited number of trials, and the outcomes in routine clinical practice and in unselected patients are scarcely reported. MethodsThe study included a consecutive series of patients with resectable gastric cancer treated between 2001 and 2011 in Central Norway. Before 2007, patients with resectable gastric cancer did not receive perioperative chemotherapy. Since 2007, medically fit patients with resectable gastric cancer and aged 75 years or less have been offered this. Response rates were evaluated by CT, and tolerability was assessed by the frequency of hospital admission, need for dose reduction or treatment discontinuation. The two time intervals were compared on an intention-to-treat basis for patients aged no more than 75 years for any impact on resection rates, surgical morbidity, postoperative mortality and long-term survival. ResultsAbout two-thirds (259) of the 419 patients registered were aged 75 years or less at diagnosis. Ninety-five of 136 patients in the later interval were eligible for chemotherapy, of whom 90 actually received the specified regimen, and 78 (87 per cent) were able to complete the preoperative course. Only 40 (44 per cent) completed all scheduled preoperative and postoperative cycles. Thirty-eight (43 per cent) of 89 evaluable patients showed a definite response on CT. Chemotherapy had no impact on postoperative morbidity or mortality. The 5-year survival rate on an intention-to-treat basis was 407 (95 per cent c.i. 307 to 507) per cent in the first interval, compared with 417 (315 to 519) per cent after the introduction of perioperative chemotherapy (P=0765). After adjustment for other risk factors, based on comparisons of the two time intervals, there were no differences in oncological outcomes with the use of perioperative chemotherapy. ConclusionPerioperative chemotherapy was completed in less than half of the patients with resectable gastric cancer. An observed tumour response to chemotherapy did not translate into any long-term survival benefit compared with surgery alone. No benefit from chemotherapy over surgery alone
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收藏
页码:1712 / 1720
页数:9
相关论文
共 24 条
[1]   Guidelines for the management of oesophageal and gastric cancer [J].
Allum, William H. ;
Blazeby, Jane M. ;
Griffin, S. Michael ;
Cunningham, David ;
Jankowski, Janusz A. ;
Wong, Rachel .
GUT, 2011, 60 (11) :1449-1472
[2]   Subtotal versus total gastrectomy for gastric cancer -: Five-year survival rates in a multicenter randomized Italian trial [J].
Bozzetti, F ;
Marubini, E ;
Bonfanti, G ;
Miceli, R ;
Piano, C ;
Gennari, L .
ANNALS OF SURGERY, 1999, 230 (02) :170-178
[3]   Outcomes among patients treated for gastric adenocarcinoma during the last decade [J].
Bringeland, E. A. ;
Wasmuth, H. H. ;
Johnsen, G. ;
Johnsen, T. B. ;
Juel, I. S. ;
Mjones, P. ;
Uggen, P. E. ;
Ystgaard, B. ;
Gronbech, J. E. .
JOURNAL OF SURGICAL ONCOLOGY, 2013, 107 (07) :752-757
[4]   The UK NCRI MAGIC trial of perioperative chemotherapy in resectable gastric cancer: Implications for clinical practice [J].
Chua, Yu Jo ;
Cunningham, David .
ANNALS OF SURGICAL ONCOLOGY, 2007, 14 (10) :2687-2690
[5]   Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer [J].
Cunningham, David ;
Allum, William H. ;
Stenning, Sally P. ;
Thompson, Jeremy N. ;
Van de Velde, Cornelis J. H. ;
Nicolson, Marianne ;
Scarffe, J. Howard ;
Lofts, Fiona J. ;
Falk, Stephen J. ;
Iveson, Timothy J. ;
Smith, David B. ;
Langley, Ruth E. ;
Verma, Monica ;
Weeden, Simon ;
Chua, Yu Jo .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (01) :11-20
[6]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[7]   Neo-adjuvant chemotherapy for operable gastric cancer: long term results of the Dutch randomised FAMTX trial [J].
Hartgrink, HH ;
van de Velde, CJH ;
Putter, H ;
Songun, I ;
Tesselaar, MET ;
Kranenbarg, EK ;
de Vries, JE ;
Wils, JA ;
van der Bijl, J ;
van Krieken, JHJM .
EJSO, 2004, 30 (06) :643-649
[8]   Introducing national guidelines on perioperative chemotherapy for gastric cancer in Norway: A retrospective audit [J].
Holmebakk, T. ;
Frykholm, G. ;
Viste, A. .
EJSO, 2010, 36 (07) :610-616
[9]   Current role of CT in Imaging of the stomach [J].
Horton, KM ;
Fishman, EK .
RADIOGRAPHICS, 2003, 23 (01) :75-87
[10]   2 HISTOLOGICAL MAIN TYPES OF GASTRIC CARCINOMA - DIFFUSE AND SO-CALLED INTESTINAL-TYPE CARCINOMA - AN ATTEMPT AT A HISTO-CLINICAL CLASSIFICATION [J].
LAUREN, P .
ACTA PATHOLOGICA ET MICROBIOLOGICA SCANDINAVICA, 1965, 64 (01) :31-&