Impact of resolved hepatitis B virus infection on clinical outcomes in patients with diffuse large B-cell lymphoma: a supplementary analysis of JCOG0601.

Int J HematolSep 27, 2026 (epub)
Clinical ResearchHematologyInfectious DiseasesOpen access

Shinya Hagiwara, Shigeru Kusumoto, Ryunosuke Machida et al.

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In 30 seconds

This supplementary analysis of the randomized JCOG0601 phase II/III trial examined whether resolved hepatitis B virus infection was associated with outcomes in patients with previously untreated, HBsAg-negative diffuse large B-cell lymphoma receiving rituximab-containing CHOP-based therapy. Among 405 patients with baseline serology, 87 were anti-HBc-positive. They were older than anti-HBc-negative patients, but progression-free and overall survival did not differ significantly: 3-year PFS was 78% vs. 81%, and 3-year OS was 90% vs. 90%, respectively. HBV reactivation occurred in five anti-HBc-positive patients.

Key findings

  • Among 405 patients, 87 were anti-HBc-positive and 318 were anti-HBc-negative.
  • Anti-HBc-positive patients were older (median age, 63 vs. 61 years; p = 0.008).
  • Three-year PFS was 78% vs. 81%, and 3-year OS was 90% vs. 90%, with no significant differences between groups.
  • HBV reactivation occurred in five anti-HBc-positive patients.

Why it matters

These findings suggest that, in this trial population, resolved HBV infection was not associated with inferior lymphoma survival during rituximab-containing CHOP-based treatment. The observed reactivations also underscore that HBV reactivation remains a relevant outcome to monitor when interpreting treatment safety, even when survival outcomes are similar by baseline anti-HBc status.

What to keep in mind

This was a supplementary analysis of a clinical trial, not a randomized comparison of anti-HBc status; the anti-HBc-positive subgroup included 87 patients.

Source

Published in Int J Hematol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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