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Ronny Allan
UPDATE – Sep 25th, 2023
– Novartis radioligand therapy Lutathera® demonstrated statistically significant and clinically meaningful progression-free survival in first line advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs)
Phase III NETTER-2 trial met primary endpoint of improvement in progression-free survival (PFS) and key secondary endpoint of objective response rate (ORR) in patients with Grade 2 and 3 advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs) who received first line treatment with Lutathera® in combination with long-acting octreotide, versus high-dose long-acting octreotide alone.
Lutathera is the first radioligand therapy (RLT) to demonstrate clinically meaningful benefit in a first line setting.
Findings to be presented at an upcoming medical meeting and discussed with regulatory authorities, with submissions to follow
What this great news means for NET patients is not yet clear, but the implications suggest a first line use of PRRT (Lutathera) in the patient populations covered in the trial. I guess any changes would need to be agreed via NET guidelines.
Novartis announcement – click here
My original blog on NETTER-2 – click here or on the graphic below:

What is Peptide Receptor Radionuclide Therapy (i.e. Radioligand Therapy)?
click here or on the picture below.

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Sep 25th, 2023
UPDATE
Novartis radioligand therapy Lutathera® demonstrated statistically significant and clinically meaningful progression-free survival in first line advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs)
Phase III NETTER-2 trial met primary endpoint of improvement in progression-free survival (PFS) and key secondary endpoint of objective response rate (ORR) in patients with Grade 2 and 3 advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs) who received first line treatment with Lutathera® in combination with long-acting octreotide, versus high-dose long-acting octreotide alone.
Lutathera is the first radioligand therapy (RLT) to demonstrate clinically meaningful benefit in a first line setting.
Findings to be presented at an upcoming medical meeting and discussed with regulatory authorities, with submissions to follow
What this great news means for NET patients is not yet clear but the implications suggest a first line use of PRRT (Lutathera) in the patient populations covered in the trial. I guess that would need to be agreed via NET guidelines.
Novartis announcement here:
My original blog on NETTER-2 can be found here:
