International Prognostic Score for Nodular Lymphocyte-Predominant Hodgkin Lymphoma.
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333
Informations de publication
Date de publication:
26 Mar 2024
26 Mar 2024
Historique:
medline:
26
3
2024
pubmed:
26
3
2024
entrez:
26
3
2024
Statut:
aheadofprint
Résumé
Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a rare cancer, and large international cooperative efforts are needed to evaluate the significance of clinical risk factors and immunoarchitectural patterns (IAPs) for all stages of pediatric and adult patients with NLPHL. Thirty-eight institutions participated in the Global nLPHL One Working Group retrospective study of NLPHL cases from 1992 to 2021. We measured progression-free survival (PFS), overall survival (OS), transformation rate, and lymphoma-specific death rate. We performed uni- and multivariable (MVA) Cox regression stratified by management to select factors for the lymphocyte-predominant international prognostic score (LP-IPS) validated by five-fold cross-validation. We identified 2,243 patients with a median age of 37 years (IQR, 23-51). The median follow-up was 6.3 years (IQR, 3.4-10.8). Most had stage I to II (72.9%) and few B symptoms (9.9%) or splenic involvement (5.4%). IAP was scored for 916 (40.8%). Frontline management included chemotherapy alone (32.4%), combined modality therapy (30.5%), radiotherapy alone (24.0%), observation after excision (4.6%), rituximab alone (4.0%), active surveillance (3.4%), and rituximab and radiotherapy (1.1%). The PFS, OS, transformation, and lymphoma-specific death rates at 10 years were 70.8%, 91.6%, 4.8%, and 3.3%, respectively. On MVA, IAPs were not associated with PFS or OS, but IAP E had higher risk of transformation (hazard ratio [HR], 1.81; In this comprehensive study of all ages of patients with NLPHL, we develop the LP-IPS to identify high-risk patients and inform upcoming prospective clinical trials evaluating de-escalation of therapy for patients with low LP-IPS scores (<2).
Identifiants
pubmed: 38531001
doi: 10.1200/JCO.23.01655
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
JCO2301655Investigateurs
Peter Borchmann
(P)
Michael Fuchs
(M)
Sylvia Hartmann
(S)
Hans Theodor Eich
(HT)
Andrea Lo
(A)
Brian Skinnider
(B)
M Shahzad Rauf
(MS)
Irfan Maghfoor
(I)
Chelsea C Pinnix
(CC)
Sarah A Milgrom
(SA)
Francisco Vega
(F)
Mohammed Alomari
(M)
Graham Collins
(G)
Ranjana H Advani
(RH)
Monika L Metzger
(ML)
Andrew Wirth
(A)
Richard Tsang
(R)
Sonali Smith
(S)
Christopher R Kelsey
(CR)
Pamela McKay
(P)
Julie Koenig
(J)
Louis S Constine
(LS)
Ku G Sakthivel
(KG)
John P Plastaras
(JP)
Sarah Gao
(S)
Nasser Al Rahbi
(N)
Mario Levis
(M)
Akshay Sridhar
(A)
Nimish Shah
(N)
Wendy Osborne
(W)
Isabela Chang
(I)
Fiona Miall
(F)
George Mikhaeel
(G)
Anthony Penn
(A)
Egor Vasilevich Volchkov
(EV)
Roberta Della Pepa
(R)
Michael Northend
(M)
Stephen Opat
(S)
Ross Salvaris
(R)
Aditya Tedjaseputra
(A)
Monica Palese
(M)
Ananth Shankar
(A)
Yasodha Natkunam
(Y)
Kara M Kelly
(KM)