Primary refractory follicular lymphoma: a poor outcome entity with high risk of transformation to aggressive B cell lymphoma.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
11 2021
Historique:
received: 17 12 2020
revised: 28 07 2021
accepted: 05 08 2021
pubmed: 12 9 2021
medline: 1 12 2021
entrez: 11 9 2021
Statut: ppublish

Résumé

Primary refractory (PREF) follicular lymphoma (FL) has a completely different clinical course from that of FL that responds to front-line treatments. In addition to having poor responses to salvage therapies, it seems that patients with PREF are at increased risk of histological transformation (HT). The Aristotle consortium presented the opportunity of investigating the risk of HT in a very large series of cases. Thus, we investigated the risk of HT in patients with PREF FL compared with that of responding patients or in stable disease and ultimately their outcome. Six thousand three hundred thirty-nine patients from the Aristotle database were included in the analysis. These patients had a histologically confirmed grade 1, 2 or 3a FL diagnosed between 1997 and 2013. The primary end-points were the cumulative incidence (CI) of HT at the first progression or relapse and the survival after transformation. The 5-year CI of HT among patients with PREF was 34% (95% confidence interval (CI): 27-43), whilst it was 7.1% (95% CI: 6.0-8.5) in the group of patients with partial response (PR) or stable disease (SD) (PR + SD) and 3.5% (95% CI: 3.0-4.2) in the group of patients achieving complete response (CR). The 5-year survival after relapse (SAR) was 33% (95% CI: 28-39) for the PREF group, 57% (95% CI 54-61) in patients with PR, 51% (95% CI 43-58) in the SD group after first-line therapy and 63% (95% CI: 66-72) in patients with CR after initial treatment (p-value <0.001). The 5-year SAR for those patients with PREF who developed HT was 21% (95% CI: 12-31), clearly diminished when compared with those patients with PREF who did not experience HT (38% [95% CI: 31-44]) (p-value = 0.001). Patients with PREF FL have a dismal outcome and an associated very high rate of HT that further worsens their poor prognosis.

Sections du résumé

BACKGROUND
Primary refractory (PREF) follicular lymphoma (FL) has a completely different clinical course from that of FL that responds to front-line treatments. In addition to having poor responses to salvage therapies, it seems that patients with PREF are at increased risk of histological transformation (HT). The Aristotle consortium presented the opportunity of investigating the risk of HT in a very large series of cases. Thus, we investigated the risk of HT in patients with PREF FL compared with that of responding patients or in stable disease and ultimately their outcome.
METHODS
Six thousand three hundred thirty-nine patients from the Aristotle database were included in the analysis. These patients had a histologically confirmed grade 1, 2 or 3a FL diagnosed between 1997 and 2013. The primary end-points were the cumulative incidence (CI) of HT at the first progression or relapse and the survival after transformation.
FINDINGS
The 5-year CI of HT among patients with PREF was 34% (95% confidence interval (CI): 27-43), whilst it was 7.1% (95% CI: 6.0-8.5) in the group of patients with partial response (PR) or stable disease (SD) (PR + SD) and 3.5% (95% CI: 3.0-4.2) in the group of patients achieving complete response (CR). The 5-year survival after relapse (SAR) was 33% (95% CI: 28-39) for the PREF group, 57% (95% CI 54-61) in patients with PR, 51% (95% CI 43-58) in the SD group after first-line therapy and 63% (95% CI: 66-72) in patients with CR after initial treatment (p-value <0.001). The 5-year SAR for those patients with PREF who developed HT was 21% (95% CI: 12-31), clearly diminished when compared with those patients with PREF who did not experience HT (38% [95% CI: 31-44]) (p-value = 0.001).
INTERPRETATION
Patients with PREF FL have a dismal outcome and an associated very high rate of HT that further worsens their poor prognosis.

Identifiants

pubmed: 34508995
pii: S0959-8049(21)00521-9
doi: 10.1016/j.ejca.2021.08.005
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

132-139

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Sara Alonso-Álvarez (S)

Department of Haematology, Hospital Universitario Central de Asturias, Spain. Electronic address: saralonsoalvarez@gmail.com.

Martina Manni (M)

CHIMOMODepartment, University of Modena and Reggio Emilia, Modena, Italy.

Silvia Montoto (S)

St Bartholomew's Hospital, Barts Health NHS Trust, London, United Kingdom.

Clémentine Sarkozy (C)

INSERM 1052, Charles Mérieux Lyon-1 Faculty, Claude Bernard University, Lyon, France.

Franck Morschhauser (F)

Department of Clinical Haematology, CHU Lille, Unite GRITA, Universite de Lille 2, Lille, France.

Marielle J Wondergem (MJ)

Department of Hematology, VU University Medical Center, Amsterdam, the Netherlands.

Attilio Guarini (A)

Haematology Unit, IRCCS IstitutoTumori "Giovanni Paolo II", Bari, Italy.

Laura Magnano (L)

Department of Haematology, Hospital Clinic of Barcelona, Spain.

Miguel Alcoceba (M)

Department of Hematology, Hospitalario Universitario de Salamanca (HUS/IBSAL) and CIBERONC, Salamanca, Spain.

Martine Chamuleau (M)

Department of Hematology, VU University Medical Center, Amsterdam, the Netherlands.

Sara Galimberti (S)

Section of Hematology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Maria Gomes da Silva (M)

Instituto Português de Oncologia, Departamento de Hematologia, Lisboa, Portugal.

Harald Holte (H)

Department of Oncology, Radiumhospitalet, Oslo University Hospital, Norway.

Emanuele Zucca (E)

Oncology Institute of Southern Switzerland (IOSI), Ospedale San Giovanni, Bellinzona, Switzerland.

Sandra Lockmer (S)

Dep. of Hematology, Karolinska University Hospital and Dep. of Medicine, Karolinska Institutet, Stockholm, Sweden.

Igor Aurer (I)

Division of Hematology, Department of Internal Medicine, University Hospital Center Zagreb and Medical School, University of Zagreb, Croatia.

Luigi Marcheselli (L)

Fondazione Italiana Linfomi (FIL) Onlus, Modena, Italy.

Yana Stepanishyna (Y)

CHIMOMODepartment, University of Modena and Reggio Emilia, Modena, Italy; Department of Oncohematology, National Cancer Institute, Kiev, Ukraine.

María Dolores Caballero Barrigón (MD)

Department of Hematology, Hospitalario Universitario de Salamanca (HUS/IBSAL) and CIBERONC, Salamanca, Spain.

Gilles Salles (G)

Gilles SALLES, Lymphoma Service, Memorial Sloan Kettering Cancer Center, NY, USA.

Massimo Federico (M)

CHIMOMODepartment, University of Modena and Reggio Emilia, Modena, Italy.

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Classifications MeSH