Literature DB >> 32730585

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

Sabela Bobillo1,2, Erel Joffe1, Jessica A Lavery3, David Sermer1, Paola Ghione1, Ariela Noy1, Philip C Caron1, Audrey Hamilton1, Paul A Hamlin1, Steven M Horwitz1, Anita Kumar1, Matthew J Matasar1, Alison Moskowitz1, Collette N Owens1, M Lia Palomba1, Connie L Batlevi1, David Straus1, Gottfried von Keudell1, Andrew D Zelenetz1, Joachim Yahalom4, Ahmet Dogan5, Venkatraman E Seshan3, Anas Younes1.   

Abstract

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.
© 2021 by The American Society of Hematology.

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Year:  2021        PMID: 32730585      PMCID: PMC8555387          DOI: 10.1182/blood.2020005112

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   25.476


  25 in total

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2.  Diffuse large B-cell lymphoma: clinical and biological characterization and outcome according to the nodal or extranodal primary origin.

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Journal:  J Clin Oncol       Date:  2005-02-22       Impact factor: 44.544

3.  First-line treatment for primary testicular diffuse large B-cell lymphoma with rituximab-CHOP, CNS prophylaxis, and contralateral testis irradiation: final results of an international phase II trial.

Authors:  Umberto Vitolo; Annalisa Chiappella; Andrés J M Ferreri; Maurizio Martelli; Ileana Baldi; Monica Balzarotti; Chiara Bottelli; Annarita Conconi; Henry Gomez; Armando Lopez-Guillermo; Giovanni Martinelli; Francesco Merli; Domenico Novero; Lorella Orsucci; Vincenzo Pavone; Umberto Ricardi; Sergio Storti; Mary K Gospodarowicz; Franco Cavalli; Andreas H Sarris; Emanuele Zucca
Journal:  J Clin Oncol       Date:  2011-06-06       Impact factor: 44.544

4.  Benefit of consolidative radiation therapy in patients with diffuse large B-cell lymphoma treated with R-CHOP chemotherapy.

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Review 5.  Chemotherapy alone for localized diffuse large B-cell lymphoma.

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6.  Chemotherapy alone compared with chemotherapy plus radiotherapy for localized intermediate- and high-grade non-Hodgkin's lymphoma.

Authors:  T P Miller; S Dahlberg; J R Cassady; D J Adelstein; C M Spier; T M Grogan; M LeBlanc; S Carlin; E Chase; R I Fisher
Journal:  N Engl J Med       Date:  1998-07-02       Impact factor: 91.245

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8.  Primary breast non-Hodgkin's lymphoma: a large single center study of initial characteristics, natural history, and prognostic factors.

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Journal:  Am J Hematol       Date:  2009-03       Impact factor: 10.047

9.  Continued Risk of Relapse Independent of Treatment Modality in Limited-Stage Diffuse Large B-Cell Lymphoma: Final and Long-Term Analysis of Southwest Oncology Group Study S8736.

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Journal:  J Clin Oncol       Date:  2016-07-05       Impact factor: 44.544

10.  R-CHOP 14 with or without radiotherapy in nonbulky limited-stage diffuse large B-cell lymphoma.

Authors:  Thierry Lamy; Gandhi Damaj; Pierre Soubeyran; Emmanuel Gyan; Guillaume Cartron; Krimo Bouabdallah; Rémy Gressin; Jérôme Cornillon; Anne Banos; Katell Le Du; Mohamed Benchalal; Marie-Pierre Moles; Steven Le Gouill; Joel Fleury; Pascal Godmer; Hervé Maisonneuve; Eric Deconinck; Roch Houot; Kamel Laribi; Jean Pierre Marolleau; Olivier Tournilhac; Bernard Branger; Anne Devillers; Jean Philippe Vuillez; Thierry Fest; Philippe Colombat; Valérie Costes; Vanessa Szablewski; Marie C Béné; Vincent Delwail
Journal:  Blood       Date:  2017-10-23       Impact factor: 25.476

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  6 in total

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2.  Stage I DLBCL: extranodal may mean extra radiation.

Authors:  Izidore S Lossos
Journal:  Blood       Date:  2021-01-07       Impact factor: 25.476

Review 3.  Molecular Genetics of Relapsed Diffuse Large B-Cell Lymphoma: Insight into Mechanisms of Therapy Resistance.

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Review 4.  Evolution of therapy for limited stage diffuse large B-cell lymphoma.

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Journal:  Blood Cancer J       Date:  2022-02-24       Impact factor: 11.037

5.  Site-Specific Survival of Extra Nodal Diffuse Large B-Cell Lymphoma and Comparison With Gastrointestinal Diffuse Large B-Cell Lymphoma.

Authors:  Varsha Gupta; Vinit Singh; Ravneet Bajwa; Trishala Meghal; Shuvendu Sen; David Greenberg; Madhurima Anne; Michael J Levitt
Journal:  J Hematol       Date:  2022-04-22

6.  5-Hydroxymethylation alterations in cell-free DNA reflect molecular distinctions of diffuse large B cell lymphoma at different primary sites.

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  6 in total

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