Results for kemoteraapia translation from Estonian to English

kemoteraapia
chemotherapy

kaasuv kemoteraapia
concomitant chemotherapy

kemoteraapia (n = 47)
chemotherapy (n = 47)

197 kaasuv kemoteraapia:
 197 include mucositis, diarrhoea, neutropaenia, renal impairment, and electrolyte disturbance.

eelnev tsütotoksiline kemoteraapia
prior exposure to cytotoxic agents

kt rühm (ainult kemoteraapia):
ct arm (chemotherapy alone):

ainult kemoteraapia (n=116)
chemo only (n=116)

kemoteraapia + avastin (n=227)
chemotherapy + avastin (n=227)

tugevalt emetogeense kemoteraapia raviskeem
highly emetogenic chemotherapy regimen

kemoteraapia järgneb mabthera infusioonile.
the chemotherapy should be given after mabthera infusion.

ravikuur väga emetogeense kemoteraapia korral
highly emetogenic chemotherapy regimen

radioteraapia või kemoteraapia ei ole kohased.
lesions are not ulcerated or lymphoedematous, and treatment of visceral ks is not required, and lesions are not responding to systemic antiretroviral therapy, and radiotherapy or chemotherapy are not appropriate

ravikuur mõõdukalt emetogeense kemoteraapia korral
moderately emetogenic chemotherapy regimen

kemoteraapia raviskeem samaaegsel kasutamisel koos imatiniibiga
chemotherapy regimen used in combination with imatinib

eelnev kemoteraapia ei sisaldanud alimta’t.
prior chemotherapy did not include alimta.

avastin’i kombineeriti kahe kemoteraapia raviskeemiga:
avastin was combined with two chemotherapy regimens:

kogufaas: 0...120 tundi pärast kemoteraapia algust.
overall phase: 0 to 120 hours following initiation of chemotherapy.

tabel 3 kemoteraapia raviskeem samaaegsel kasutamisel koos imatiniibiga
table 3 chemotherapy regimen used in combination with imatinib

induktsioon kemoteraapia, millele järgneb kemoradioteraapia (tax 324)
induction chemotherapy followed by chemoradiotherapy (tax 324)

pärast karboplatiini- paklitakseeli kemoteraapia kuue tsükli läbimist või
patients were randomized to platinum-based chemotherapy (paclitaxel 200 mg/ m2 and carboplatin auc = 6.0, both by iv infusion) (pc) on day 1 of every 3-week cycle for up to 6 cycles or pc in combination with avastin at a dose of 15 mg/ kg iv infusion day 1 of every 3-week cycle.