AI Article Synopsis

  • Systemic anaplastic large-cell lymphoma (sALCL) is a rare and aggressive form of T-cell lymphoma that often has a poor prognosis after relapse, but brentuximab vedotin (BV) has been used since 2013 to improve outcomes.
  • A population-based study in England analyzed the results for 127 patients with relapsed sALCL treated with BV between 2014 and 2019, finding a median overall survival rate of 46.6% at two years.
  • Patients who received BV as their second line of treatment had a significantly better survival rate compared to those treated later, highlighting the importance of early intervention.

Article Abstract

Systemic anaplastic large-cell lymphoma (sALCL) is a rare T-cell lymphoma associated with poor prognosis after relapse. The immunoconjugate brentuximab vedotin (BV) first became available for relapsed sALCL in England in 2013, following the results of a pivotal phase II study. We present a population-based study describing outcomes of relapsed sALCL in England after BV, using Public Health England data. We obtained information on all relapsed/refractory (r/r) sALCL patients ≥18 years treated with BV monotherapy in England between 1 January 2014 and 31 December 2019. The final cohort comprised 127 patients with a median age of 60 years (range 19-89). Eighteen (14·2%) had received stem cell transplant in first remission. Median two-year overall survival (OS) was 46·6%. The vast majority of deaths (59) occurred within 18 months, with very few events after this. Receipt of BV as second line compared to third or fourth line was associated with significantly improved survival (two-year OS 50·3% vs 29·7%, P = 0·03). There was no difference in OS for different subgroups, including anaplastic lymphoma kinase status, age, gender, or receipt of stem cell transplantation in first response. We report excellent survival following treatment with BV in a real-world setting, comparable with previous clinical trial data.

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http://dx.doi.org/10.1111/bjh.17896DOI Listing

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