Haematologica (Oct 2020)

Hodgkin lymphoma arising in patients with chronic lymphocytic leukemia: outcomes from a large multi-center collaboration

  • Deborah M. Stephens,
  • Ken Boucher,
  • Elizabeth Kander,
  • Sameer A. Parikh,
  • Erin M. Parry,
  • Mazyar Shadman,
  • John M. Pagel,
  • Jennifer Cooperrider,
  • Joanna Rhodes,
  • Anthony Mato,
  • Allison Winter,
  • Brian Hill,
  • Sameh Gaballa,
  • Alexey Danilov,
  • Tycel Phillips,
  • Danielle M. Brander,
  • Sonali M. Smith,
  • Matthew Davids,
  • Kerry Rogers,
  • Martha J. Glenn,
  • John C. Byrd

DOI
https://doi.org/10.3324/haematol.2020.256388
Journal volume & issue
Vol. 106, no. 11

Abstract

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Chronic lymphocytic leukemia (CLL) patients who develop Hodgkin lymphoma (HL) have limited survival. No current therapeutic standard of care exists. We conducted a multi-center retrospective study of patients with Hodgkin transformation (HT) of CLL. Clinicobiologic characteristics, treatment type, and survival outcomes were analyzed and compared with historic case series. Ninety-four patients were identified. Median age at HT was 67 years (range, 38-85). Median time from CLL diagnosis to HT was 5.5 years (range, 0-20.2). Prior to HT, patients received a median of two therapies for CLL (range, 0-12). As initial therapy for HT, 61% (n=62) received ABVD-based regimens (adriamycin, bleomycin, vinblastine, and dacarbazine). Seven (7%) patients received hematopoietic cell transplantation (HCT) while in first complete remission (CR1). The median number of treatments for HT per patient was one (range, 0-5) with 59 (61%) patients only receiving one line of therapy. After HT, patients had a median follow-up of 1.6 years (range, 0-15.1). Two-year overall survival (OS) after HT diagnosis was 72% (95% Confidence Interval: 62-83). The patients who received standard ABVD-based therapy had a median OS of 13.2 years. Although limited by small sample size, the patients who underwent HCT for HT in CR1 had a similar 2-year OS (n=7; 67%) compared to patients who did not undergo HCT for HT in CR1 (n=87; 72%; P=0.46). In this multi-center study, HT patients treated with ABVD-based regimens had prolonged survival supporting the use of these regimens as standard of care for these patients.