-
Je něco špatně v tomto záznamu ?
Gastroduodenal, intestinal and colonic permeability during anticancer therapy
B. Melichar, R. Hyspler, H. Kalábová, J. Dvorák, A. Tichá, Z. Zadák
Jazyk angličtina Země Řecko
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21937377
DOI
10.5754/hge08101
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- duodenum metabolismus MeSH
- kolon metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- permeabilita MeSH
- protinádorové látky farmakokinetika MeSH
- sacharosa analogy a deriváty farmakokinetika MeSH
- senioři MeSH
- střevní sliznice metabolismus MeSH
- žaludeční sliznice metabolismus MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND/AIMS: Measurement of the permeability of gut mucosa may offer a method for objective assessment of mucosal dysfunction during cancer therapy. METHODOLOGY: Gastroduodenal, intestinal and colonic permeability was studied by using capillary gas chromatography and measuring urinary sucralose, sucrose, lactulose, xylose and mannitol levels. A total of 41 patients with metastatic colorectal carcinoma or epithelial ovarian carcinoma were studied before and during chemotherapy with the combinations of cetuximab, irinotecan, 5-fluorouracil and leucovorin; bevacizumab, oxaliplatin, 5-fluorouracil and leucovorin; or paclitaxel/ platinum. RESULTS: Compared to pretreatment values, a significant increase was observed during the first cycle of therapy in the percentage of sucrose, sucrose/mannitol ratio, lactulose and lactulose/ mannitol ratio in patients treated with the combination of bevacizumab, oxaliplatin, 5-fluorouracil and leucovorin. No changes were observed in patients treated with cetuximab, irinotecan, 5-fluorouracil and leucovorin, but these patients had significantly higher baseline percentage of lactulose excretion and sucrose/mannitol and lactulose/ mannitol ratios. CONCLUSIONS: An increase in gastroduodenal and intestinal permeability was observed in patients treated with bevacizumab, oxaliplatin, 5-fluorouracil and leucovorin, but not in patients treated with cetuximab, irinotecan, 5-fluorouracil and leucovorin. No significant increase in colonic permeability was observed, but the present method was insufficient to detect colonic permeability in a significant proportion of patients.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12022301
- 003
- CZ-PrNML
- 005
- 20160405114740.0
- 007
- ta
- 008
- 120806s2011 gr f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.5754/hge08101 $2 doi
- 035 __
- $a (PubMed)21937377
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gr
- 100 1_
- $a Melichar, Bohuslav, $d 1965- $7 skuk0000853 $u Department of Oncology and Radiotherapy, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic. bohuslav.melichar@fnol.cz
- 245 10
- $a Gastroduodenal, intestinal and colonic permeability during anticancer therapy / $c B. Melichar, R. Hyspler, H. Kalábová, J. Dvorák, A. Tichá, Z. Zadák
- 520 9_
- $a BACKGROUND/AIMS: Measurement of the permeability of gut mucosa may offer a method for objective assessment of mucosal dysfunction during cancer therapy. METHODOLOGY: Gastroduodenal, intestinal and colonic permeability was studied by using capillary gas chromatography and measuring urinary sucralose, sucrose, lactulose, xylose and mannitol levels. A total of 41 patients with metastatic colorectal carcinoma or epithelial ovarian carcinoma were studied before and during chemotherapy with the combinations of cetuximab, irinotecan, 5-fluorouracil and leucovorin; bevacizumab, oxaliplatin, 5-fluorouracil and leucovorin; or paclitaxel/ platinum. RESULTS: Compared to pretreatment values, a significant increase was observed during the first cycle of therapy in the percentage of sucrose, sucrose/mannitol ratio, lactulose and lactulose/ mannitol ratio in patients treated with the combination of bevacizumab, oxaliplatin, 5-fluorouracil and leucovorin. No changes were observed in patients treated with cetuximab, irinotecan, 5-fluorouracil and leucovorin, but these patients had significantly higher baseline percentage of lactulose excretion and sucrose/mannitol and lactulose/ mannitol ratios. CONCLUSIONS: An increase in gastroduodenal and intestinal permeability was observed in patients treated with bevacizumab, oxaliplatin, 5-fluorouracil and leucovorin, but not in patients treated with cetuximab, irinotecan, 5-fluorouracil and leucovorin. No significant increase in colonic permeability was observed, but the present method was insufficient to detect colonic permeability in a significant proportion of patients.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a protinádorové látky $x farmakokinetika $7 D000970
- 650 _2
- $a kolon $x metabolismus $7 D003106
- 650 _2
- $a duodenum $x metabolismus $7 D004386
- 650 _2
- $a žaludeční sliznice $x metabolismus $7 D005753
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a střevní sliznice $x metabolismus $7 D007413
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a permeabilita $7 D010539
- 650 _2
- $a sacharosa $x analogy a deriváty $x farmakokinetika $7 D013395
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Hyšpler, Radomír, $d 1972- $7 nlk20040155091
- 700 1_
- $a Kalábová, Hana. $7 xx0240731
- 700 1_
- $a Dvořák, Josef, $d 1966- $7 xx0072583
- 700 1_
- $a Tichá, Alena, $d 1976- $7 xx0076494
- 700 1_
- $a Zadák, Zdeněk, $d 1937- $7 nlk19990074064
- 773 0_
- $w MED00002025 $t Hepato-gastroenterology $x 0172-6390 $g Roč. 58, č. 109 (2011), s. 1193-1199
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21937377 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m $z 0
- 990 __
- $a 20120806 $b ABA008
- 991 __
- $a 20160405114816 $b ABA008
- 999 __
- $a ok $b bmc $g 944214 $s 779598
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 58 $c 109 $d 1193-1199 $i 0172-6390 $m Hepato-gastroenterology $n Hepatogastroenterology $x MED00002025
- LZP __
- $b NLK111 $a Pubmed-20120806/12/01