Survival outcomes of patients with extranodal natural-killer T-cell lymphoma: a prospective cohort study from the international T-cell Project.


Journal

The Lancet. Haematology
ISSN: 2352-3026
Titre abrégé: Lancet Haematol
Pays: England
ID NLM: 101643584

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 29 08 2019
revised: 10 12 2019
accepted: 17 12 2019
pubmed: 28 2 2020
medline: 9 4 2020
entrez: 28 2 2020
Statut: ppublish

Résumé

Extranodal natural killer (NK) T-cell lymphoma (ENKTL) is a unique clinicopathological entity, typically associated with poor survival outcomes. Most published data have come from east Asian study groups, with little information available from international cohorts. The effects of treatment advances on routine clinical practice across continental territories has not been clear. We aimed to improve understanding of the clinical characteristics and outcomes of patients with ENKTL. We did a substudy of patients with ENKTL from the T-cell Project, a global prospective cohort study. The T-cell Project registered consecutively diagnosed adults (>18 years) with newly diagnosed, untreated mature T-cell or NK lymphomas (WHO 2001 or 2008 classifications) from 74 centres in 13 countries (in Asia, Europe, North America, and South America). In total, 1695 patients with mature T-cell or NK lymphomas were enrolled between Oct 12, 2006 and Feb 28, 2018 in the T-cell Project. The first patient with ENKTL was enrolled on Feb 15, 2007, and the last on May 26, 2017. Data on baseline characteristics, first-line treatment, treatment response, and survival outcomes were recorded in a central database (locked March 30, 2019). The primary outcome was 5-year overall survival. The T-cell Project is registered on ClinicalTrials.gov, NCT01142674. 166 patients were diagnosed with ENKTL, comprising 11% of 1553 eligible registered cases and distributed across 40 participating centres in four continents. At a median follow-up of 44 months (IQR 20-61), overall survival at 5 years was 54% (95% CI 44-63) in patients with nasal disease (n=98) and 34% (27-46) in patients with extranasal disease (n=68). To our knowledge, this study presents the largest international cohort of patients with ENKTL. We describe a clinically significant improvement in the survival of patients with ENKTL treated in routine clinical practice over the past decade, likely to be attributable to the increasing use of treatment protocols specific for ENKTL. The Fondazione Cassa di Risparmio di Modena, the Associazione Angela Serra per la Ricerca sul Cancro, the Fondazione Italiana Linfomi, Allos Therapeutics, Spectrum Pharmaceuticals, Associazione Italiana per la Ricerca sul Cancro, and the National Cancer Institute at the National Institutes of Health.

Sections du résumé

BACKGROUND BACKGROUND
Extranodal natural killer (NK) T-cell lymphoma (ENKTL) is a unique clinicopathological entity, typically associated with poor survival outcomes. Most published data have come from east Asian study groups, with little information available from international cohorts. The effects of treatment advances on routine clinical practice across continental territories has not been clear. We aimed to improve understanding of the clinical characteristics and outcomes of patients with ENKTL.
METHODS METHODS
We did a substudy of patients with ENKTL from the T-cell Project, a global prospective cohort study. The T-cell Project registered consecutively diagnosed adults (>18 years) with newly diagnosed, untreated mature T-cell or NK lymphomas (WHO 2001 or 2008 classifications) from 74 centres in 13 countries (in Asia, Europe, North America, and South America). In total, 1695 patients with mature T-cell or NK lymphomas were enrolled between Oct 12, 2006 and Feb 28, 2018 in the T-cell Project. The first patient with ENKTL was enrolled on Feb 15, 2007, and the last on May 26, 2017. Data on baseline characteristics, first-line treatment, treatment response, and survival outcomes were recorded in a central database (locked March 30, 2019). The primary outcome was 5-year overall survival. The T-cell Project is registered on ClinicalTrials.gov, NCT01142674.
FINDINGS RESULTS
166 patients were diagnosed with ENKTL, comprising 11% of 1553 eligible registered cases and distributed across 40 participating centres in four continents. At a median follow-up of 44 months (IQR 20-61), overall survival at 5 years was 54% (95% CI 44-63) in patients with nasal disease (n=98) and 34% (27-46) in patients with extranasal disease (n=68).
INTERPRETATION CONCLUSIONS
To our knowledge, this study presents the largest international cohort of patients with ENKTL. We describe a clinically significant improvement in the survival of patients with ENKTL treated in routine clinical practice over the past decade, likely to be attributable to the increasing use of treatment protocols specific for ENKTL.
FUNDING BACKGROUND
The Fondazione Cassa di Risparmio di Modena, the Associazione Angela Serra per la Ricerca sul Cancro, the Fondazione Italiana Linfomi, Allos Therapeutics, Spectrum Pharmaceuticals, Associazione Italiana per la Ricerca sul Cancro, and the National Cancer Institute at the National Institutes of Health.

Identifiants

pubmed: 32105608
pii: S2352-3026(19)30283-2
doi: 10.1016/S2352-3026(19)30283-2
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT01142674']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e284-e294

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Christopher P Fox (CP)

Department of Clinical Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.

Monica Civallero (M)

CHIMOMO Department, University of Modena and Reggio Emilia, Modena, Italy.

Young-Hyeh Ko (YH)

Department of Pathology, Sungkyunkwan University, Seoul, South Korea.

Martina Manni (M)

CHIMOMO Department, University of Modena and Reggio Emilia, Modena, Italy.

Tetiana Skrypets (T)

CHIMOMO Department, University of Modena and Reggio Emilia, Modena, Italy.

Stefano Pileri (S)

Division of Haematopathology, Istituto Europeo di Oncologia, Milano, Italy.

Seok Jin Kim (SJ)

Division of Hematology-Oncology, Samsung Medical Center, Seoul, South Korea.

Maria Elena Cabrera (ME)

Sección Hematología, Hospital del Salvador, Universidad de Chile, Santiago, Chile.

Andrei R Shustov (AR)

Division of Hematology, Fred Hutchinson Cancer Research Center, University of Washington Medical Center, Seattle, WA, USA.

Carlos S Chiattone (CS)

Departamento de Clínica Médica, Faculdade de Ciências Médicas Santa Casa de São Paulo, São Paulo, Brazil; Centro de Linfomas Núcleo de Oncologia Hospital Samaritano, São Paulo, Brazil.

Steven M Horwitz (SM)

Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Ivan Dlouhy (I)

Hematology Department, Hospital Clinic de Barcelona, Barcelona, Spain.

Michele Spina (M)

Division of Medical Oncology A, Aviano National Cancer Institute, Aviano, Italy.

Felicitas Hitz (F)

The Swiss Group for Clinical Cancer Research, Department of Oncology/Haematology, Cantonal Hospital, St Gallen, Switzerland.

Silvia Montoto (S)

Department of Haematology, Barts Health NHS Trust, London, UK.

Arnon Nagler (A)

Department of Bone Marrow Transplantation, Tel Aviv University, Tel Aviv, Israel.

Virginia Martinez (V)

Instituto de Anatomía Patologica, Santiago, Chile.

Carmino A De Souza (CA)

Departamento de Clínica Médica, Universidade Estadual de Campinas, Campinas, Brazil.

Ruben Fernandez-Alvarez (R)

Department of Hematology, Hospital de Cabueñes, Asturias, Spain.

Veronika Ballova (V)

Department of Internal Medicine, National Oncology and Hematology Institute, Bratislava, Slovakia.

Raul Gabús (R)

Hematology and Bone Marrow Transplantation Service, Hospital Maciel, Montevideo, Uruguay.

Giorgio Inghirami (G)

Department of Pathology, Columbia University College of Physicians and Surgeons, New York, NY, USA.

Massimo Federico (M)

CHIMOMO Department, University of Modena and Reggio Emilia, Modena, Italy.

Won Seog Kim (WS)

Division of Hematology-Oncology, Samsung Medical Center, Seoul, South Korea. Electronic address: wskimsmc@skku.edu.

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Classifications MeSH