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Clinical and pathological characteristics of peripheral T-cell lymphomas in a Spanish population: a retrospective study.

Authors :
Rodriguez-Pinilla SM
Domingo-Domenech E
Climent F
Sanchez J
Perez Seoane C
Lopez Jimenez J
Garcia-Cosio M
Caballero D
Blanco Muñez OJ
Carpio C
Castellvi J
Martinez Pozo A
Gonzalez Farre B
Bendaña A
Aliste C
Gonzalez AJ
Gonzalez de Villambrosia S
Piris MA
Gomez Codina J
Mayordomo-Aranda E
Navarro B
Bellas C
Rodriguez G
Borrero JJ
Ruiz-Zorrilla A
Grande M
Montoto C
Cordoba R
Source :
British journal of haematology [Br J Haematol] 2021 Jan; Vol. 192 (1), pp. 82-99. Date of Electronic Publication: 2020 May 19.
Publication Year :
2021

Abstract

We investigated the clinicopathological features and prognostic factors of patients with peripheral T-cell lymphoma (PTCL) in 13 sites across Spain. Relevant clinical antecedents, CD30 expression and staining pattern, prognostic indices using the International Prognostic Index and the Intergruppo Italiano Linfomi system, treatments, and clinical outcomes were examined. A sizeable proportion of 175 patients had a history of immune-related disorders (autoimmune 16%, viral infections 17%, chemo/radiotherapy-treated carcinomas 19%). The median progression-free survival (PFS) and overall survival (OS) were 7·9 and 15·8 months, respectively. Prognostic indices influenced PFS and OS, with a higher number of adverse factors resulting in shorter survival (P < 0·001). Complete response (CR) to treatment was associated with better PFS (62·6 vs. 4 months; P < 0·001) and longer OS (67·0 vs. 7·3 months; P < 0·001) compared to no CR. CD30 was expressed across all subtypes; >15% of cells were positive in anaplastic lymphoma kinase-positive and -negative anaplastic large-cell lymphoma and extranodal natural killer PTCL groups. We observed PTCL distribution across subtypes based on haematopathological re-evaluation. Poor prognosis, effect of specific prognostic indices, relevance of histopathological sub-classification, and response level to first-line treatment on outcomes were confirmed. Immune disorders amongst patients require further examination involving genetic studies and identification of associated immunosuppressive factors.<br /> (© 2020 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2141
Volume :
192
Issue :
1
Database :
MEDLINE
Journal :
British journal of haematology
Publication Type :
Academic Journal
Accession number :
32426847
Full Text :
https://doi.org/10.1111/bjh.16741