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Impact of liver tumour burden, alkaline phosphatase elevation, and target lesion size on treatment outcomes with 177Lu-Dotatate: an analysis of the NETTER-1 study.

Jonathan R StrosbergPamela L KunzAndrew HendifarJames YaoDavid BushnellMatthew H KulkeRichard P BaumMartyn CaplinPhilippe RuszniewskiEbrahim DelpassandTimothy HobdayChris VerslypeAl BensonRajaventhan SrirajaskanthanMarianne PavelJaume MoraJordan BerlinEnrique GrandeNicholas ReedEttore SeregniGiovanni PaganelliStefano SeveriMichael MorseDavid C MetzCatherine AnsquerFrédéric CourbonAdil Al-NahhasEric BaudinFrancesco GiammarileDavid TaïebErik MittraEdward WolinThomas M O'DorisioRachida LebtahiChristophe M DerooseChiara M GranaLisa BodeiKjell ÖbergBerna Degirmenci PolackBeilei HeMaurizio F MarianiGermo GerickePaola SantoroJack L ErionLaura RavasiEric Krenningnull null
Published in: European journal of nuclear medicine and molecular imaging (2020)
177Lu-Dotatate demonstrated significant prolongation in PFS versus high-dose octreotide LAR in patients with advanced, progressive midgut NET, regardless of baseline liver tumour burden, elevated ALP, or the presence of a large target lesion. Clinicaltrials.gov : NCT01578239, EudraCT: 2011-005049-11.
Keyphrases
  • neuroendocrine tumors
  • high dose
  • pet ct
  • multiple sclerosis
  • low dose
  • risk factors
  • stem cell transplantation
  • drug induced
  • aedes aegypti
  • zika virus