Clinical characteristics and outcomes of extranodal stage I diffuse large B-cell lymphoma in the rituximab era.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
07 01 2021
Historique:
received: 28 01 2020
accepted: 01 07 2020
pubmed: 31 7 2020
medline: 17 4 2021
entrez: 31 7 2020
Statut: ppublish

Résumé

This retrospective study aimed to better define the characteristics and outcomes of extranodal stage I diffuse large B-cell lymphoma (DLBCL) in the rituximab era. Patients diagnosed with stage I DLBCL from 2001 to 2015 treated with rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP) or R-CHOP-like regimens with or without radiation (RT) were included. We identified 1955 patients with newly diagnosed DLBCL, of whom 341 had stage I and were eligible for this analysis. Extranodal presentation was observed in 224 (66%) patients, whereas 117 (34%) had nodal involvement. The most common extranodal sites were as follows: bone, 21%; stomach, 19%; testis, 9%; intestine, 8%; breast, 8%. Overall, 69% extranodal patients and 68% nodal patients received RT. Median follow-up was 5.5 years (interquartile range, 4.3-8.2). Ten-year overall survival (OS) and disease-free survival were 77% (95% confidence interval [CI], 67%-83%) and 77% (95% CI, 68%-85%). In the multivariable analyses, extranodal involvement was associated with worse OS (hazard ratio [HR], 3.44; 95% CI, 1.05-11.30) and progression-free survival (PFS; HR, 3.25; 95% CI, 1.08-9.72) compared with nodal involvement. Consolidation RT was associated with better OS (HR, 0.26; 95% CI, 0.12-0.49) and PFS (HR, 0.35; 95% CI, 0.18-0.69) in the extranodal population; however, the benefit was no longer observed in patients that were positron emission tomography (PET) negative at the end of immunochemotherapy. Relapses occurred usually late (median, 37 months), and the most common sites were the lymph nodes (31%) and the central nervous system (27%). Extranodal stage I DLBCL had a worse outcome than nodal stage 1 DLBCL. End of immunochemotherapy PET results may help select extranodal patients for consolidation RT.

Identifiants

pubmed: 32730585
pii: S0006-4971(20)86004-2
doi: 10.1182/blood.2020005112
pmc: PMC8555387
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Rituximab 4F4X42SYQ6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-48

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

Sabela Bobillo (S)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Department of Hematology, Vall d'Hebron University Hospital, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain; and.

Erel Joffe (E)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Jessica A Lavery (JA)

Department of Epidemiology and Biostatistics.

David Sermer (D)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Paola Ghione (P)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Ariela Noy (A)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Philip C Caron (PC)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Audrey Hamilton (A)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Paul A Hamlin (PA)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Steven M Horwitz (SM)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Anita Kumar (A)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Matthew J Matasar (MJ)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Alison Moskowitz (A)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Collette N Owens (CN)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

M Lia Palomba (ML)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Connie L Batlevi (CL)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

David Straus (D)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Gottfried von Keudell (G)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Andrew D Zelenetz (AD)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Joachim Yahalom (J)

Department of Radiation Oncology, and.

Ahmet Dogan (A)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.

Venkatraman E Seshan (VE)

Department of Epidemiology and Biostatistics.

Anas Younes (A)

Lymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

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