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SWOG S1826

Immunotherapy plus chemotherapy beat the previous best regimen with far less nerve damage, in the first Hodgkin trial to enrol children and adults together; approved March 2026.

1-year PFS 94% vs 86%; 2-year PFS 92% vs 83% (HR 0.45, NEJM 2024). Peripheral neuropathy 28.1% vs 54.2%; fewer treatment discontinuations. Radiotherapy given to <1%. FDA approval 20 March 2026 for ages 12+. Now the frontline standard for advanced-stage disease in North America; HD21's BrECADD is the European alternative.

Setting
Untreated stage III-IV classical Hodgkin lymphoma, age ≥12: nivolumab + AVD vs brentuximab vedotin + AVD
Phase
Phase 3
Sponsor
SWOG / NCI (with COG)
Registry
Headline result
2-year PFS 92% vs 83%, HR 0.45.
Reported
2023
Enrolled
994
Replication
Consistent with phase 2 N-AVD data (CheckMate 205 cohort D) and with pembrolizumab-AVD single-arm studies; no second randomised trial yet.

Outcomes

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In plain words
What these results mean for people, not percentages
994 people took part
Progression-free survival at 2 yearsprimarysurrogate endpoint
  • 92 vs 83 out of 100 alive without the cancer growing at 2 years with Nivolumab-AVD compared with BV-AVD; 9 more per 100.
  • Roughly one extra person helped for every 11 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 55 percent lower chance of the event at any given time (hazard ratio 0.45, likely range 0.3 to 0.65).
  • 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.
Any-grade peripheral neuropathyother endpoint
  • 28.1 vs 54.2 out of 100 reached this endpoint with Nivolumab-AVD compared with BV-AVD; 26.1 fewer per 100.
  • On this measure the first group did worse, not better.
  • This endpoint is not one of the standard survival or response measures; read it alongside the trial's primary result.
Be careful
  • These results apply to the people the trial enrolled: Untreated stage III-IV classical Hodgkin lymphoma, age ≥12: nivolumab + AVD vs brentuximab vedotin + AVD. 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.

994 participants enrolled.

Progression-free survival at 2 yearsprimary
HR 0.45 (0.3–0.65) · p <0.001
Nivolumab-AVD92 of 100
n = 489
BV-AVD83 of 100
n = 487
Source
Any-grade peripheral neuropathy
Nivolumab-AVD28.1 of 100
BV-AVD54.2 of 100
EndpointArmnValueHR (95% CI)pSource
Progression-free survival at 2 yearsprimaryNivolumab-AVD48992%0.45 (0.3–0.65)<0.001link
BV-AVD48783%
Any-grade peripheral neuropathyNivolumab-AVD28.1%
BV-AVD54.2%
Replication
Consistent with phase 2 N-AVD data (CheckMate 205 cohort D) and with pembrolizumab-AVD single-arm studies; no second randomised trial yet.

Key papers

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Connected

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Pages like this

not linked directly; found by shared links