Chemotherapy of advanced small-bowel adenocarcinoma: a multicenter AGEO study

被引:116
作者
Zaanan, A. [2 ]
Costes, L. [3 ]
Gauthier, M. [4 ]
Malka, D. [3 ]
Locher, C. [5 ]
Mitry, E. [6 ]
Tougeron, D. [7 ]
Lecomte, T. [8 ]
Gornet, J. -M. [9 ]
Sobhani, I. [10 ]
Moulin, V. [11 ]
Afchain, P. [2 ]
Taieb, J. [12 ]
Bonnetain, F. [4 ]
Aparicio, T. [1 ]
机构
[1] Univ Paris 13, Hop Avicenne, AP HP, Dept Gastroenterol,Serv Gastroenterol, F-93009 Bobigny, France
[2] Univ Paris 06, Dept Med Oncol, St Antoine Hosp, AP HP, F-75252 Paris 05, France
[3] Univ Paris 11, Dept Med, Inst Gustave Roussy, Villejuif, France
[4] Georges Francois Leclerc Ctr, Biostat & Epidemiol Unit, Dijon, France
[5] Meaux Hosp, Dept Hepatogastroenterol, Meaux, France
[6] Ambroise Pare Hosp, AP HP, Dept Hepatogastroenterol & Digest Oncol, Boulogne, France
[7] Charles Nicolle Hosp, Dept Hepatogastroenterol, Rouen, France
[8] Univ Tours, Dept Hepatogastroenterol, Trousseau Hosp, Tours, France
[9] St Louis Hosp, AP HP, Dept Hepatogastroenterol, Paris, France
[10] Henri Mondor Hosp, AP HP, Dept Hepatogastroenterol, Creteil, France
[11] Louis Pasteur Hosp, Dept Med Oncol, Coudray, France
[12] Europeen Georges Pompidou Hosp, AP HP, Dept Hepatogastroenterol, Paris, France
关键词
chemotherapy; prognostic factor; small-bowel adenocarcinoma; METASTATIC COLORECTAL-CANCER; ADVANCED ESOPHAGOGASTRIC CANCER; RANDOMIZED-TRIAL; PHASE-II; CONTINUOUS-INFUSION; 1ST-LINE TREATMENT; PROGNOSTIC-FACTORS; VENOUS INFUSION; FLUOROURACIL; 5-FLUOROURACIL;
D O I
10.1093/annonc/mdq038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Small-bowel adenocarcinoma (SBA) is a rare tumor of poor prognosis. Data on the efficacy of chemotherapy for advanced SBA are scarce. Patients and methods: All patients with advanced SBA who received frontline chemotherapy from 1996 to 2008 were eligible for this retrospective multicenter study. Results: Ninety-three consecutive patients were included. In the entire population, the median progression-free survival (PFS) and overall survival (OS) times were 6.6 and 15.1 months, respectively. Median PFS times among patients treated with LV5FU2 (n = 10), FOLFOX (n = 48), FOLFIRI (n = 19) and LV5FU2-cisplatin (n = 16) were 7.7, 6.9, 6.0 and 4.8 months, respectively, while median OS times were 13.5, 17.8, 10.6 and 9.3 months, respectively. In multivariate analysis, World Health Organization performance status (PS) (P < 0.0001) and elevated serum levels of carcinoembryonic antigen (CEA) (P = 0.02) and carbohydrate antigen 19-9 (CA 19-9) (P = 0.03) were the only variables significantly associated with poor OS. In the subgroup of patients treated with platinum-based chemotherapy, multivariate analysis showed that LV5FU2-cisplatin was associated with poorer PFS (P < 0.0001) and OS (P = 0.02) compared with FOLFOX. Conclusions: This is the largest study of chemotherapy in advanced SBA. Baseline PS and CEA and CA 19-9 levels were the main prognostic factors. FOLFOX seems to be the most effective platinum-based chemotherapy regimen.
引用
收藏
页码:1786 / 1793
页数:8
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