TY - JOUR
T1 - Stage I-II nodular lymphocyte-predominant Hodgkin lymphoma
T2 - a multi-institutional study of adult patients by ILROG
AU - Binkley, Michael S
AU - Rauf, M Shahzad
AU - Milgrom, Sarah A
AU - Pinnix, Chelsea C
AU - Tsang, Richard
AU - Dickinson, Michael
AU - Ng, Andrea K
AU - Roberts, Kenneth B
AU - Gao, Sarah
AU - Balogh, Alex
AU - Ricardi, Umberto
AU - Levis, Mario
AU - Casulo, Carla
AU - Stolten, Michael
AU - Specht, Lena
AU - Plastaras, John P
AU - Wright, Christopher
AU - Kelsey, Christopher R
AU - Brady, Jessica L
AU - Mikhaeel, N George
AU - Hoppe, Bradford S
AU - Terezakis, Stephanie A
AU - Picardi, Marco
AU - Della Pepa, Roberta
AU - Kirova, Youlia
AU - Akhtar, Saad
AU - Maghfoor, Irfan
AU - Koenig, Julie L
AU - Jackson, Christopher
AU - Song, Erin
AU - Sehgal, Shuchi
AU - Advani, Ranjana H
AU - Natkunam, Yasodha
AU - Constine, Louis S
AU - Eich, Hans T
AU - Wirth, Andrew
AU - Hoppe, Richard T
N1 - © 2020 by The American Society of Hematology.
PY - 2020/6/25
Y1 - 2020/6/25
N2 - 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.
AB - 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.
U2 - 10.1182/blood.2019003877
DO - 10.1182/blood.2019003877
M3 - Journal article
C2 - 32211877
SN - 0006-4971
VL - 135
SP - 2365
EP - 2374
JO - Blood
JF - Blood
IS - 26
ER -