| Literature DB >> 33054118 |
Deborah M Stephens1, Ken Boucher2, Elizabeth Kander3, Sameer A Parikh4, Erin M Parry5, Mazyar Shadman6, John M Pagel7, Jennifer Cooperrider8, Joanna Rhodes9, Anthony Mato10, Allison Winter11, Brian Hill11, Sameh Gaballa12, Alexey Danilov13, Tycel Phillips14, Danielle M Brander15, Sonali M Smith8, Matthew Davids5, Kerry Rogers3, Martha J Glenn2, John C Byrd3.
Abstract
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 2 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 1 (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%CI 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.Entities:
Year: 2020 PMID: 33054118 DOI: 10.3324/haematol.2020.256388
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941