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trialsTrialPositive

HIMALAYA

A single dose of a CTLA-4 antibody added to PD-L1 blockade doubled five-year survival in liver cancer without needing an anti-VEGF drug.

OS 16.4 vs 13.8 months (HR 0.78); five-year OS 19.6% vs 9.4% (ESMO 2024 / 2025 publication), the longest follow-up of any phase 3 in HCC. No bleeding risk from anti-VEGF, so usable in patients with varices. Durvalumab monotherapy was non-inferior to sorafenib.

Setting
First-line unresectable HCC: STRIDE (single priming dose tremelimumab + durvalumab) vs sorafenib
Phase
Phase 3
Sponsor
AstraZeneca
Registry
Headline result
OS HR 0.78; 5-year OS 19.6% vs 9.4%.
Reported
2022
Enrolled
1171
Replication
Five-year follow-up of the same trial; the STRIDE + TACE strategy is being tested in EMERALD-3.

Outcomes

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In plain words
What these results mean for people, not percentages
1,171 people took part
Overall survivalprimarysurvival endpoint
  • Median 16.4 vs 13.8 months with STRIDE compared with Sorafenib; about 2.6 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 22 percent lower chance of the event at any given time (hazard ratio 0.78, likely range 0.66 to 0.92).
5-year overall survivalsurvival endpoint
  • 19.6 vs 9.4 out of 100 alive at 5 years with STRIDE compared with Sorafenib; 10.2 more per 100.
  • Roughly one extra person helped for every 10 treated. That is a rough figure taken from the two percentages, not a guarantee for any one person.
  • Put another way, the treated group had about 24 percent lower chance of the event at any given time (hazard ratio 0.76).
Be careful
  • 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: First-line unresectable HCC: STRIDE (single priming dose tremelimumab + durvalumab) vs sorafenib. 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.

1,171 participants enrolled.

Overall survivalprimary
HR 0.78 (0.66–0.92)
STRIDE
16.4 mo
Sorafenib
13.8 mo
5-year overall survival
HR 0.76
STRIDE19.6 of 100
Sorafenib9.4 of 100
Source
EndpointArmnValueHR (95% CI)pSource
Overall survivalprimarySTRIDE39316.4 months0.78 (0.66–0.92)
Sorafenib38913.8 months
5-year overall survivalSTRIDE19.6%0.76link
Sorafenib9.4%
Replication
Five-year follow-up of the same trial; the STRIDE + TACE strategy is being tested in EMERALD-3.

Connected

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