OnCo
trialsTrialPositive

LATITUDE

LATITUDE established abiraterone at first metastatic diagnosis for high-risk disease.

1,199 men; OS 53.3 vs 36.5 months (HR 0.66) at final analysis.

Setting
High-risk de novo metastatic hormone-sensitive prostate cancer: ADT + abiraterone vs ADT
Phase
Phase 3
Sponsor
Janssen
Registry
Headline result
OS HR 0.66.
Reported
2017
Enrolled
1199
Replication
Replicated by STAMPEDE arm G.

Outcomes

1top
In plain words
What these results mean for people, not percentages
1,199 people took part
Overall survivalprimarysurvival endpoint
  • Median 53.3 vs 36.5 months with ADT + abiraterone compared with ADT + placebo; about 16.8 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 34 percent lower chance of the event at any given time (hazard ratio 0.66, likely range 0.56 to 0.78).
  • Overall survival counts deaths from any cause, so it is the most direct measure of whether a treatment helps people live longer.
  • These results apply to the people the trial enrolled: High-risk de novo metastatic hormone-sensitive prostate cancer: ADT + abiraterone vs ADT. People in a different situation may not see the same effect.

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.

1,199 participants enrolled.

Overall survivalprimary
HR 0.66 (0.56–0.78) · p <0.0001
ADT + abiraterone
53.3 mo
ADT + placebo
36.5 mo
Source
EndpointArmnValueHR (95% CI)pSource
Overall survivalprimaryADT + abiraterone59753.3 months0.66 (0.56–0.78)<0.0001link
ADT + placebo60236.5 months
Replication
Replicated by STAMPEDE arm G.

Connected

5top