[177Lu]Lu-edotreotide versus everolimus for gastroenteropancreatic neuroendocrine tumours (COMPETE): a phase 3, multicentre, randomised, open-label, superiority trial.
What this study shows
Phase 3 open-label RCT (n=309, 2:1): 177Lu-edotreotide gave longer PFS than everolimus (23.9 vs 14.1 months; HR 0.67) with fewer grade 3-4 treatment-related adverse events (18% vs 40%), supporting PRRT in early lines for progressive SSTR-positive GEP-NETs.
At a glance
| Evidence type | H Human study Marked H because it is direct evidence from a human clinical trial or human cohort; the code names the kind of study, not its quality -- a small, well-run trial is still H. |
| Study type | 2 - Human Clinical Trial |
| Model system | Human RCT |
| Journal | Lancet |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1016/S0140-6736(26)00604-5 · PMID 42392118 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Everolimus (mTOR inhibitor) vs [177Lu]Lu-edotreotide |
| Target | mTORC1 |
| Model | Human |
| Effect | PRRT ([177Lu]Lu-edotreotide) gave longer PFS than everolimus, with fewer grade 3-4 treatment-related adverse events, in treatment-naive or pretreated SSTR-positive GEP-NETs |
In the Atlas
Related topics
More studies on this topic
- Everolimus for advanced pancreatic neuroendocrine tumors (RADIANT-3) (2011)
- Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer (BOLERO-2) (2012)
- Everolimus for angiomyolipoma associated with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis (EXIST-2): a multicentre, randomised, double-blind, placebo-controlled trial (2013)
- Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): a multicentre, randomised, placebo-controlled phase 3 trial (2013)
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