Oral glutamine in the prevention of fluorouracil induced intestinal toxicity: a double blind, placebo controlled, randomised trial

B Daniele, F Perrone, C Gallo, S Pignata, S De Martino, R De Vivo, E Barletta, R Tambaro, R Abbiati, L D'Agostino, B Daniele, F Perrone, C Gallo, S Pignata, S De Martino, R De Vivo, E Barletta, R Tambaro, R Abbiati, L D'Agostino

Abstract

Background: 5-Fluorouracil (FU) in association with folinic acid (FA) is the most frequently used chemotherapeutic agent in colorectal cancer but it often causes diarrhoea. Animal and human studies suggest that glutamine stimulates intestinal mucosal growth.

Aim: To determine if oral glutamine prevents changes in intestinal absorption (IA) and permeability (IP) induced by FU/FA.

Methods: Seventy chemotherapy naive patients with colorectal cancer were randomly assigned to oral glutamine (18 g/day) or placebo before the first cycle of FU (450 mg/m(2)) and FA (100 mg/m(2)) administered intravenously for five days. Treatment was continued for 15 days, starting five days before the beginning of chemotherapy. IA (D-xylose urinary excretion) and IP (cellobiose-mannitol test) were assessed at baseline and four and five days after the end of the first cycle of chemotherapy, respectively. Patients kept a daily record of diarrhoea, scored using the classification system of the National Cancer Institute (Bethesda, Maryland, USA). Duration of diarrhoea was recorded and the area under the curve (AUC) was calculated for each patient.

Results: Baseline patient characteristics and basal values of IP and IA tests were similar in the two arms. After one cycle of chemotherapy, the reduction in IA (D-xylose absorption) was more marked in the placebo arm (7.1% v 3. 8%; p=0.02); reduction of IP to mannitol was higher in the placebo arm (9.2% v 4.5%; p=0.02); and urinary recovery of cellobiose was not different between the study arms (p=0.60). Accordingly, the cellobiose-mannitol ratio increased more in the placebo arm (0.037 v 0.012; p=0.04). Average AUC of diarrhoea (1.9 v 4.5; p=0.09) and average number of loperamide tablets taken (0.4 v 2.6; p=0.002) were reduced in the glutamine arm.

Conclusions: Glutamine reduces changes in IA and IP induced by FU and may have a protective effect on FU induced diarrhoea.

Figures

Figure 1
Figure 1
Box plots of pre- (open boxes) and post- (shaded boxes) treatment values for intestinal absorption and intestinal permeability parameters. Solid lines indicate the 5th, 25th, 50th, 75th, and 95th percentiles; broken lines indicate mean values; solid dots indicate upper and lower values.
Figure 2
Figure 2
Box plots of area under the curve (AUC) values by treatment arm for all patients (open boxes) and for those with diarrhoea (shaded boxes). Solid lines indicate the 5th, 25th, 50th, 75th, and 95th percentiles; broken lines indicate mean values; solid dots indicate upper and lower values.

References

    1. Br J Exp Pathol. 1980 Apr;61(2):132-8
    1. Gastroenterology. 1995 May;108(5):1566-81
    1. Gastroenterology. 1994 Dec;107(6):1595-601
    1. Br J Exp Pathol. 1977 Dec;58(6):663-9
    1. J Clin Oncol. 1989 Oct;7(10):1407-18
    1. J Biol Chem. 1974 Aug 25;249(16):5070-9
    1. Cancer. 1990 Jul 1;66(1):62-8
    1. Gut. 1999 Jul;45(1):82-8
    1. Gastroenterology. 1994 Apr;106(4):899-906
    1. Dig Dis Sci. 1991 Feb;36(2):188-92
    1. Exp Mol Pathol. 1992 Apr;56(2):96-107
    1. Gut. 1984 Nov;25(11):1241-6
    1. Gastroenterology. 1994 Dec;107(6):1885-6
    1. Lancet. 1993 May 29;341(8857):1363-5
    1. Ann Oncol. 1996 Nov;7(9):901-6
    1. Cancer Res. 1980 Oct;40(10):3430-6
    1. Clin Nutr. 1991 Aug;10(4):193-8
    1. Clin Sci Mol Med. 1978 Apr;54(4):411-8
    1. Cancer. 1992 May 1;69(9):2343-8
    1. Br J Cancer. 1994 Oct;70(4):732-5
    1. Dig Dis Sci. 1989 Apr;34(4):553-8
    1. Gastroenterology. 1988 Jul;95(1):223-31
    1. Cancer. 1998 Oct 1;83(7):1433-9
    1. Scand J Gastroenterol. 1990 Apr;25(4):321-8
    1. J Clin Oncol. 1987 Oct;5(10):1559-65
    1. Cancer. 1978 Oct;42(4):1747-59
    1. J Biol Chem. 1980 Jan 10;255(1):107-12
    1. JPEN J Parenter Enteral Nutr. 1988 Jul-Aug;12(4):325-31
    1. J Biol Chem. 1978 Jan 10;253(1):69-76
    1. J Clin Oncol. 1995 Jun;13(6):1303-11
    1. Annu Rev Nutr. 1991;11:285-308
    1. Clin Nutr. 1991 Aug;10(4):186-92
    1. BMJ. 1990 Jan 27;300(6719):230-5
    1. Gut. 1989 Apr;30(4):476-80

Source: PubMed

3
Suscribir