Outcomes in grade 3B follicular lymphoma: an international study led by the Australasian Lymphoma Alliance.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 09 2023
Historique:
received: 09 05 2022
medline: 8 9 2023
pubmed: 24 2 2023
entrez: 23 2 2023
Statut: epublish

Résumé

Grade (G) 3B follicular lymphoma (FL) is a rare FL subtype which exists on a histological continuum between 'lowgrade' (Grade 1, 2 and 3A FL) and diffuse large B-cell lymphoma (DLBCL) appearing to share features with each. Clinical characteristics and outcomes are poorly understood due to lack of adequate representation in prospective trials and large-scale analyses. We analyzed 157 G3BFL cases from 18 international centers, and two comparator groups; G3AFL (n=302) and DLBCL (n=548). Composite histology with DLBCL or low-grade FL occurred in approximately half of the G3BFL cases. With a median of 5 years follow-up, the overall survival and progression-free survival of G3BFL patients was better than that of DLBCL patients (P<0.001 and P<0.001, respectively); however, G3BFL patients were younger (P<0.001) with better performance status (P<0.001), less extranodal disease (P<0.001) and more frequently had normal lactate dehydrogenase (P<0.001) at baseline. The overall and progression-free survival of patients with G3BFL and G3AFL were similar (P=0.83 and P=0.80, respectively). After frontline immunochemotherapy, 24% of G3BFL relapsed; relapse rates were 63% in the DLBCL cohort and 19% in the low-grade FL cohort. Eight percent of relapses occurred beyond 5 years. In this G3BFL cohort, the revised International Prognostic Index successfully delineated risk groups, but the Follicular Lymphoma International Prognostic Index did not. We conclude that patients with immunochemotherapy-treated G3BFL have similar survival outcomes to those with G3AFL, yet a favorable baseline profile and distinctly superior prognosis compared to patients with DLBCL.

Identifiants

pubmed: 36815381
doi: 10.3324/haematol.2022.281375
pmc: PMC10483350
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2444-2453

Commentaires et corrections

Type : CommentIn

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Auteurs

Allison Barraclough (A)

Fiona Stanley Hospital, Department of Haematology, Perth, Australia; University of Melbourne, Melbourne.

James T England (JT)

University of British Columbia and BC Cancer Centre for Lymphoid Cancer, Vancouver, Canada; Princess Margaret Cancer Centre, Toronto.

Diego Villa (D)

University of British Columbia and BC Cancer Centre for Lymphoid Cancer, Vancouver.

Joel Wight (J)

University of Melbourne, Melbourne, Australia; Townsville University Hospital, Department of Haematology, Townsville.

Greg Hapgood (G)

Princess Alexandra Hospital, Department of Haematology, Brisbane.

Jason Conn (J)

Princess Alexandra Hospital, Department of Haematology, Brisbane.

Nicole Wong Doo (NW)

Concord Clinical School, University of Sydney, Sydney.

Eric Wenlong Li (EW)

Concord Clinical School, University of Sydney, Sydney.

Michael Gilbertson (M)

Monash Health, Department of Haematology, Melbourne, Australia; School of Clinical Sciences, Monash University, Melbourne.

Briony Shaw (B)

Monash Health, Department of Haematology, Melbourne.

Mark J Bishton (MJ)

Nottingham City Hospital, Department of Haematology, Nottingham.

Malik Saeed (M)

Nottingham City Hospital, Department of Haematology, Nottingham.

Sumita Ratnasingam (S)

University Hospital Geelong, Department of Haematology, Geelong.

Chathuri Abeyakoon (C)

University Hospital Geelong, Department of Haematology, Geelong.

Geoff Chong (G)

University of Melbourne, Melbourne, Australia; Ballarat Regional Integrated Cancer Centre, Ballarat Health Services, Melbourne, Australia; Department of Medical Oncology and Haematology, Olivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne.

Shin Hnin Wai (SH)

Department of Medical Oncology and Haematology, Olivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne, Australia; The Northern Hospital, Department of Haematology, Melbourne.

Matthew Ku (M)

University of Melbourne, Melbourne, Australia; St Vincent's Hospital Melbourne, Department of Haematology, Melbourne.

Hui-Peng Lee (HP)

Flinders Medical Centre, Department of Haematology, Adelaide.

Kathryn Fleming (K)

Flinders Medical Centre, Department of Haematology, Adelaide.

Constantine Tam (C)

University of Melbourne, Melbourne, Australia; Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Department of Haematology, Melbourne.

Genevieve Douglas (G)

Department of Medical Oncology and Haematology, Olivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne.

Chan Y Cheah (CY)

Sir Charles Gairdner Hospital, Department of Haematology, Perth, Australia; University of Western Australia, Medical School, Perth.

Zi Yun Ng (ZY)

Sir Charles Gairdner Hospital, Department of Haematology, Perth.

Tukten Rolfe (T)

Greenslopes Private Hospital, Brisbane.

Anthony K Mills (AK)

Greenslopes Private Hospital, Brisbane.

Nada Hamad (N)

St Vincent's Hospital Sydney, Department of Haematology, Sydney, Australia; School of Clinical Medicine, University of New South Wales, Sydney, Australia; School of Medicine, University of Notre Dame, Sydney.

Helen Cashman (H)

St Vincent's Hospital Sydney, Department of Haematology, Sydney.

Mary Gleeson (M)

Guy's and St. Thomas' NHS Foundation Trust, Department of Haematology, London.

Manjunath Narayana (M)

Sunshine Coast University Hospital, Department of Haematology, Birtinya.

Eliza A Hawkes (EA)

Department of Medical Oncology and Haematology, Olivia Newton-John Cancer Research and Wellness Centre, Austin Health, Melbourne, Australia; Transfusion Research Unit, Monash University, Melbourne. eliza.hawkes@onjcri.org.au.

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