Outcomes and prognostic factors in angioimmunoblastic T-cell lymphoma: final report from the international T-cell Project.


Journal

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

Informations de publication

Date de publication:
22 07 2021
Historique:
received: 15 12 2020
accepted: 12 03 2021
entrez: 22 7 2021
pubmed: 23 7 2021
medline: 3 9 2021
Statut: ppublish

Résumé

Angioimmunoblastic T-cell lymphoma (AITL) is a unique subtype of peripheral T-cell lymphoma (PTCL) with distinct clinicopathologic features and poor prognosis. We performed a subset analysis of 282 patients with AITL enrolled between 2006 and 2018 in the international prospective T-cell Project (NCT01142674). The primary and secondary end points were 5-year overall survival (OS) and progression-free survival (PFS), respectively. We analyzed the prognostic impact of clinical covariates and progression of disease within 24 months (POD24) and developed a novel prognostic score. The median age was 64 years, and 90% of patients had advanced-stage disease. Eighty-one percent received anthracycline-based regimens, and 13% underwent consolidative autologous stem cell transplant (ASCT) in first complete remission (CR1). Five-year OS and PFS estimates were 44% and 32%, respectively, with improved outcomes for patients who underwent ASCT in CR1. In multivariate analysis, age ≥60 years, Eastern Cooperative Oncology Group performance status >2, elevated C-reactive protein, and elevated β2 microglobulin were associated with inferior outcomes. A novel prognostic score (AITL score) combining these factors defined low-, intermediate-, and high-risk subgroups with 5-year OS estimates of 63%, 54%, and 21%, respectively, with greater discriminant power than established prognostic indices. Finally, POD24 was a powerful prognostic factor with 5-year OS of 63% for patients without POD24 compared with only 6% for patients with POD24 (P < .0001). These data will require validation in a prospective cohort of homogeneously treated patients. Optimal treatment of AITL continues to be an unmet need, and novel therapeutic approaches are required.

Identifiants

pubmed: 34292324
pii: S0006-4971(21)00754-0
doi: 10.1182/blood.2020010387
pmc: PMC8493974
doi:

Banques de données

ClinicalTrials.gov
['NCT01142674']

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

213-220

Subventions

Organisme : NCI NIH HHS
ID : P01 CA229100
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

Ranjana H Advani (RH)

Division of Oncology, Department of Medicine, Stanford University, Stanford, CA.

Tetiana Skrypets (T)

Department of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.

Monica Civallero (M)

Department of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.

Michael A Spinner (MA)

Division of Oncology, Department of Medicine, Stanford University, Stanford, CA.

Martina Manni (M)

Department of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.

Won Seog Kim (WS)

Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, South Korea.

Andrei R Shustov (AR)

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

Steven M Horwitz (SM)

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

Felicitas Hitz (F)

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

Maria Elena Cabrera (ME)

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

Ivan Dlouhy (I)

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

José Vassallo (J)

A.C. Camargo Cancer Center, Universidade Estadual de Campinas (Unicamp), Campinas, São Paulo, Brazil.

Stefano A Pileri (SA)

Division of Haematopathology, Istituto Europeo di Oncologia Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milano, Italy.

Giorgio Inghirami (G)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.

Silvia Montoto (S)

Department of Haemato-oncology, Barts Health NHS Trust, London, United Kingdom.

Umberto Vitolo (U)

Hematology, Città della Salute e della Scienza Hospital and University, Turin, Italy.

John Radford (J)

Christie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; and.

Julie M Vose (JM)

University of Nebraska Medical Center, Omaha, NE.

Massimo Federico (M)

Department of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.

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