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histologi <0,0001 4,4 gange højere hos dem med adenocarcinom end hos dem, der ikke har adenocarcinom
histology <0.0001 4.4 times higher in adenocarcinoma than in non-adenocarcinoma
· kirtelkræft i maven (gastrisk adenocarcinom) hos patienter, der endnu ikke har fået nogen
· gastric adenocarcinoma (a type of stomach cancer) in patients who have not yet received any
i en eksplorativ analyse var omfanget af fordelene ved avastin på den samlede overlevelse mindre udtalt i undergruppen af patienter, som ikke havde adenocarcinom- histologi.
in an exploratory analysis, the extent of avastin benefit on overall survival was less pronounced in the subgroup of patients who did not have adenocarcinoma histology.
en multicenter, åben, randomiseret undersøgelse har evalueret sikkerhed og effekt af docetaxel til behandling af patienter med metastatisk gastrisk adenocarcinom, inklusive adenocarcinom af den gastrooesophagele forbindelse.
a multicenter, open-label, randomized trial, was conducted to evaluate the safety and efficacy of docetaxel for the treatment of patients with metastatic gastric adenocarcinoma, including
der er registreret et tilfælde af adenom i kolon og et tilfælde af adenocarcinom i coecum hos rotter ved dosen 1500 mg/kg/dag, hvilket ikke var statistisk signifikant.
one colonic adenoma and one caecal adenocarcinoma recorded in rats at the dose of 1,500 mg/kg/day were not statistically significant.
størstedelen af patienter havde adenocarcinom (93,3 %) og havde enten aldrig været eller var tidligere rygere (96,9 %).
the vast majority of patients had adenocarcinoma (93.3%) and had either never been or were former smokers (96.9%).
hvad sker der med taxotere/ docetaxel winthrop til behandling af andre typer brystkræft, ikke- småcellet lungekræft, prostatakræft, gastrisk adenocarcinom og kræft i hoved og hals?
what is happening for taxotere/ docetaxel winthrop for the treatment of other types of breast cancer, non-small cell lung cancer, prostate cancer, gastric adenocarcinoma and head and neck cancer?
i en 21 måneders carcinogenicitetsundersøgelse af mus sås en øget forekomst af testikulære interstitialcelletumorer og prostataadenomer og -adenocarcinomer blandt hanner, som fik 41 eller 210 mg/kg, og prostataleiomyoblastomer blandt hanner, som fik 210 mg/kg.
in a 21-month carcinogenicity study in mice, there was an increased incidence of testicular interstitial cell tumours and prostatic adenomas and adenocarcinomas in males given 41 or 210 mg/kg, and prostatic leiomyoblastoma in males given 210 mg/kg.