Haematologica (Nov 2024)

Loncastuximab in high-risk and heavily pretreated relapsed / refractory diffuse large B-cell lymphoma: a real-world analysis from 21 US centers

  • Viktoriya Zelikson,
  • Ashwath Gurumurthi,
  • Yazeed Sawalha,
  • Kaitlin Annunzio,
  • Aditi Saha,
  • Ning Dong,
  • David Qualls,
  • Behzad Amoozgar,
  • Brad Kahl,
  • John Baird,
  • Pavan Challa,
  • Scott F Huntington,
  • Jennifer Santos,
  • Steven Bair,
  • Mayur Narkhede,
  • Shuning Li,
  • Zachary Frosch,
  • Carrie Ho,
  • Stephen D Smith,
  • Allison Winter,
  • Daniel Landsburg,
  • Fateeha Furqan,
  • Mehdi Hamadani,
  • Katelin Baird,
  • Jason Romancik,
  • Hanan Alharthy,
  • Jennie Law,
  • Leyla Bojanini,
  • Ranjana Advani,
  • Boyu Hu,
  • Patrick Connor Johnson,
  • Natalie S. Grover,
  • Mwanasha Merril,
  • Jennifer L. Crombie,
  • Nazila Shafagati,
  • Cole Sterling,
  • Loretta J. Nastoupil,
  • Narendranath Epperla,
  • Emily C Ayers

DOI
https://doi.org/10.3324/haematol.2024.285977
Journal volume & issue
Vol. 999, no. 1

Abstract

Read online

Outcomes in patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) are poor. Loncastuximab-teserine (Lonca) is an antibody drug conjugate (ADC) which was FDA approved for R/R DLBCL patients who have received at least 2 prior lines of therapy based on the LOTIS-2 trial. However, there are limited data regarding its efficacy in the real-world setting (RWS). This retrospective study included 21 US centers and evaluated outcomes of patients with R/R DLBCL treated with Lonca. Our analysis includes 187 patients with notably higher risk baseline features compared to LOTIS-2 including a higher proportion of patients with bulky disease (17% vs 0%), high-grade B-cell histology (HGBL) (22% vs 8%), and increased number of prior lines of therapy (median 4 vs 3). The complete response (CR) rate was 14% and overall response rate (ORR) was 32%. Median event free (EFS) and overall survival (OS) were 2.1 and 4.6 months, respectively. Those with bulky disease and HGBL had significantly worse outcomes, and those with non-germinal center cell of origin and CR to most recent line of therapy demonstrated superior outcomes. In summary, in this largest retrospective cohort study of Lonca in the RWS, the response rates, EFS, and OS were lower than those reported in LOTIS-2, which is likely reflective of its use in higher risk and more heavily pre-treated patients within the real world compared to those enrolled on clinical study.