Stage I-II nodular lymphocyte-predominant Hodgkin lymphoma: a multi-institutional study of adult patients by ILROG.
Adult
Aged
Combined Modality Therapy
/ adverse effects
Female
Follow-Up Studies
Hodgkin Disease
/ diagnostic imaging
Humans
Kaplan-Meier Estimate
Lymphoma, Large B-Cell, Diffuse
/ epidemiology
Male
Middle Aged
Neoplasm Staging
Neoplasms, Radiation-Induced
/ epidemiology
Neoplasms, Second Primary
/ epidemiology
Positron Emission Tomography Computed Tomography
Progression-Free Survival
Proportional Hazards Models
Recurrence
Retrospective Studies
Salvage Therapy
Survival Analysis
Treatment Outcome
Young Adult
Journal
Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509
Informations de publication
Date de publication:
25 06 2020
25 06 2020
Historique:
received:
23
10
2019
accepted:
06
03
2020
pubmed:
27
3
2020
medline:
20
2
2021
entrez:
27
3
2020
Statut:
ppublish
Résumé
Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is an uncommon histologic variant, and the optimal treatment of stage I-II NLPHL is undefined. We conducted a multicenter retrospective study including patients ≥16 years of age with stage I-II NLPHL diagnosed from 1995 through 2018 who underwent all forms of management, including radiotherapy (RT), combined modality therapy (CMT; RT+chemotherapy [CT]), CT, observation after excision, rituximab and RT, and single-agent rituximab. End points were progression-free survival (PFS), freedom from transformation, and overall survival (OS) without statistical comparison between management groups. We identified 559 patients with median age of 39 years: 72.3% were men, and 54.9% had stage I disease. Median follow-up was 5.5 years (interquartile range, 3.1-10.1). Five-year PFS and OS in the entire cohort were 87.1% and 98.3%, respectively. Primary management was RT alone (n = 257; 46.0%), CMT (n = 184; 32.9%), CT alone (n = 47; 8.4%), observation (n = 37; 6.6%), rituximab and RT (n = 19; 3.4%), and rituximab alone (n = 15; 2.7%). The 5-year PFS rates were 91.1% after RT, 90.5% after CMT, 77.8% after CT, 73.5% after observation, 80.8% after rituximab and RT, and 38.5% after rituximab alone. In the RT cohort, but not the CMT cohort, variant immunoarchitectural pattern and number of sites >2 were associated with worse PFS (P < .05). Overall, 21 patients (3.8%) developed large-cell transformation, with a significantly higher transformation rate in those with variant immunoarchitectural pattern (P = .049) and number of involved sites >2 (P = .0006). OS for patients with stage I-II NLPHL was excellent after all treatments.
Identifiants
pubmed: 32211877
pii: S0006-4971(20)75924-0
doi: 10.1182/blood.2019003877
doi:
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
2365-2374Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2020 by The American Society of Hematology.