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2 with gross residual disease.
2 b’marda residwali sostanzjali.
Ultimo aggiornamento 2017-04-26
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2 with or without gross residual disease.
2 bi jew mingħajr marda residwali sostanzjali.
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subgroup analyses of efs and os response indicated that patients with minimal residual disease, dna hyperploidy, and those having received a purged bone marrow may not have benefited from dinutuximab immunotherapy.
analiżijiet ta’ sottogruppi ta’ rispons efs u os indikaw li pazjenti b’mard residwu minimu, dna hyperploidy, u dawk li rċivew mudullun imnaddaf, setgħu ma bbenefikawx minn immunoterapija b’dinutuximab.
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retreatment should be given at that time if residual disease activity remains, otherwise retreatment should be delayed until disease activity returns.
kura mill-ġdid għandha tingħata f’dak il-waqt jekk tibqa’ l-attività residwali tal-marda, inkella kura mill-ġdid għandha tiġi ttardjata sakemm tirritorna l-attività tal-marda.
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major cytogenetic response, haematological response, molecular response (evaluation of minimal residual disease), time to accelerated phase or blast crisis and survival are main secondary endpoints.
dejta tar- rispons qed jintwerew f’ tabella 3.
Ultimo aggiornamento 2011-10-23
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Eliminalo se ritieni che sia così.
clinical study to evaluate minimal residual disease (mrd) for the assessment of the anti-leukaemic activity of ceplene plus low dose interleukin-2 in approximately 150 adult patients stratified by age greater or less than 60 years with acute myeloid leukemia in first complete remission.
studju kliniku biex jevalwa mard minimu residwu (mrd) għall- valutazzjoni ta 'attività antilewċemika ta' ceplene flimkien ma 'doża baxxa ta' interleukin- 2 f' madwar 150 pazjent adult stratifikati skont età ikbar jew inqas minn 60 sena b' lewċemija mjelojde akuta fl- ewwel remissjoni kompluta.
Ultimo aggiornamento 2011-10-23
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Eliminalo se ritieni che sia così.
overall approximately 34% of patients were figo stage iii optimally debulked with gross residual disease, 40% stage iii sub-optimally debulked, and 26% were stage iv patients.
globalment madwar 34% ta’ pazjenti kienu figo stadju iii bi tneħħija ottimali b’marda residwa sostanzjali, 40% kienu stadju iii bi tneħħija inqas minn ottimali, u 26% kienu pazjenti ta’ stadju iv.
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evaluate minimal residual disease (mrd) at baseline and follow-up in a clinical study or registry, as appropriate, for the assessment of the anti-leukaemic activity of ceplene plus low dose interleukin-2 in a sufficient number of adult patients stratified by age greater or less than 60 years with acute myeloid leukemia in first complete remission
evalwa mard minimu residwu (mrd - minimal residual disease) fil-linja bażi u segwi fi studju kliniku jew reġistru, kif xieraq, għall-valutazzjoni tal-attività antilewkimika ta’ ceplene flimkien ma’ doża baxxa ta’ interleukin-2 f’numru suffiċjenti ta’ pazjenti adulti stratifikati skont l-età bħala akbar jew inqas minn 60 sena b’lewkimja mjelojde akuta fl-ewwel remissjoni kompluta
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as expected on the basis of the study design, no difference was observed in remission duration, disease-free survival or overall survival, although patients with complete molecular response and remaining in minimal residual disease had a better outcome in terms of both remission duration (p = 0.01) and disease-free survival (p = 0.02).
kif mistenni mill-mod kif ġie diżenjat dan l-istudju, ma kienx hemm differenzi fit-tul taż-żmien ta’ remissjoni, sopravivenza ħielsa mill- marda jew sopravivenza globali, għalkemm il-pazjenti b’rispons molekulari komplet u li baqgħu bir- residwu minimu tal-marda kellhom konsegwenzi aħjar kemm mil-lat taż-żmien ta’ remissjoni (p=0.01) u s-sopravivenza ħielsa mill-marda (p=0.02).
Ultimo aggiornamento 2017-04-26
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