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AETHERA

In AETHERA, a year of the CD30 ADC after transplant halved relapse risk in high-risk patients.

PFS HR 0.57 (median 42.9 vs 24.1 months); no OS difference (crossover). Approved August 2015 as post-transplant consolidation.

Setting
High-risk Hodgkin lymphoma after autologous transplant: brentuximab vedotin consolidation vs placebo
Phase
Phase 3
Sponsor
Seagen
Registry
Headline result
PFS HR 0.57.
Reported
2015
Enrolled
329

Outcomes

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In plain words
What these results mean for people, not percentages
329 people took part
Progression-free survival (median)primarysurrogate endpoint
  • Median 42.9 vs 24.1 months with Brentuximab vedotin compared with Placebo; about 18.8 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 43 percent lower chance of the event at any given time (hazard ratio 0.57, likely range 0.4 to 0.81).
  • This is a surrogate endpoint: it measures the cancer being controlled or absent on scans and tests, which often, but not always, translates into living longer.
  • These results apply to the people the trial enrolled: High-risk Hodgkin lymphoma after autologous transplant: brentuximab vedotin consolidation vs placebo. 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.

329 participants enrolled.

Progression-free survival (median)primary
HR 0.57 (0.4–0.81)
Brentuximab vedotin
42.9 mo
Placebo
24.1 mo
Source
EndpointArmnValueHR (95% CI)pSource
Progression-free survival (median)primaryBrentuximab vedotin16542.9 months0.57 (0.4–0.81)link
Placebo16424.1 months

Connected

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