OnCo
trialsTrialPositive

PROMID

Showed for the first time that a hormone-suppressing injection also slows neuroendocrine tumour growth.

Time to tumour progression 14.3 vs 6.0 months (HR 0.34); no OS difference (crossover, low event rate).

Setting
Treatment-naive metastatic midgut NETs: octreotide LAR vs placebo
Phase
Phase 3
Sponsor
Novartis / German NET study group
Registry
Headline result
TTP 14.3 vs 6.0 months, HR 0.34.
Reported
2009
Enrolled
85
Replication
CLARINET extended the antiproliferative effect to lanreotide across enteropancreatic NETs.

Outcomes

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In plain words
What these results mean for people, not percentages
85 people took part
Time to tumour progressionprimaryother endpoint
  • Median 14.3 vs 6 months with Octreotide LAR compared with Placebo; about 8.3 months longer for half the group.
  • A median is a midpoint: half the people did better than this and half did worse, so it is not a prediction for any one person.
  • Put another way, the treated group had about 66 percent lower chance of the event at any given time (hazard ratio 0.34, likely range 0.2 to 0.59).
  • This endpoint is not one of the standard survival or response measures; read it alongside the trial's primary result.
  • These results apply to the people the trial enrolled: Treatment-naive metastatic midgut NETs: octreotide LAR vs placebo. People in a different situation may not see the same effect.
  • Only 85 people took part, so the numbers are less certain than in a large trial.

Numbers are from the trial as recorded here; see the source links in the table below. This is orientation, not medical advice: ask your team how closely the trial population matches you.

85 participants enrolled.

Time to tumour progressionprimary
HR 0.34 (0.2–0.59)
Octreotide LAR
14.3 mo
Placebo
6 mo
EndpointArmnValueHR (95% CI)pSource
Time to tumour progressionprimaryOctreotide LAR4214.3 months0.34 (0.2–0.59)
Placebo436 months
Replication
CLARINET extended the antiproliferative effect to lanreotide across enteropancreatic NETs.

Connected

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