THE NUMBER OF EXTRANODAL SITES IN NODAL PTCL: A PROPOSAL FOR A FEASIBLE PROGNOSTIC MARKER FOR OUTCOMES IN LOW-INCOME COUNTRIES. A COLLABORATIVE STUDY GRUPO DE ESTUDIO LATINO-AMERICANO DE LINFOPROLIFERATIVO (GELL) & T-CELL BRAZIL PROJECT (TCBP)

Autor: T Fischer, E Miranda, J Pereira, G Duffles, JV Tavares, NS Castro, RSA Silva, DLC Farias, SAB Brasil, CCG Macedo, C Colaço, RLR Baptista, KZ Cecyn, D Bortucchi, GFS Barros, S Nabhan, PPG Radtke, R Schaffel, N Zing, FL Nogueira, AD Cunha-Junior, DV Clé, JTDS Filho, VLP Figueiredo, MD Pont, R Gaiolla, N Hamerschlak, EFO Ribeiro, A Hallack-Neto, MA Dias, Y Gonzaga, YS Rabelo, L Teixeira, G Perini, MALHM Conhalato, P Cury, H Idrobo, D Castro, B Beltran, D Enriquez, J Vasquez, C Roche, D Artiles, F Valvert, L Villela, C Oliver, L Korin, C Pena, M Roa, MAT Viera, AV Gasenapp, A Quiroz, CS Figari, R Rios, S Paredes, EE Saul, C Bermack, K Meza, B Valcarcel, CA Souza, L Malpica, CS Chiattone
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S256-S258 (2024)
Druh dokumentu: article
ISSN: 2531-1379
DOI: 10.1016/j.htct.2024.09.430
Popis: Introduction: PTCL accounts for 10-15% of all NHL. As previously demonstrated, Latin America has its own epidemiological distribution, with a high frequency of ATLL and ENKT, likely influenced by distinct genetic profiles and viral epidemiology. 3-year OS is about 40%. Treatment advances have also been limited, except for BV-CHP in some countries. The IPI, which includes extranodal (EN) site as a variable, has been validated for PTCL. However, the specific impact of EN involvement on nodal PTCL (such as PTCL-NOS, AIT, ALCL ALK+/ALK-) and its biological implications remain unclear. Simplification could improve the reproducibility and applicability of these models, especially in low-income countries. Objective: To evaluate number of EN sites in nodal PTCL lymphomas as a risk factors or surrogate for outcomes, as OS and PFS in Latin America cohort. Methodology: Patients (pts) aged ≥18 years with newly diagnosed nodal PTCL-NOS, AITL and ALCL ALK+/ALK-) from GELL (n = 339, 2000-2023, retrospective), TCBP (n = 427, 2015-2022, ambispective). Treatment outcome was determined by OS and PFS. REDcap Platform (by Vanderbilt) was used to collect and store data, whereas statistical analysis the IBM-SPSS v.24. This trial is registered at Clinical trials (NCT03207789). Results: 766 pts [427pts - TCBP and 339 - GELL] diagnosed with nodal PTCL were grouped according to the number of EN: no EN involvement (No EN - 383); one EN involvement (EN1 -168); and 32 (EN2 - 215). Considering all, 61% male; median age 56 y/o; 74% were staged III/IV; 69% IPI 32; 60% was PTCL-NOS, 19% ALCL ALK- and 12% AITL. 61% had B symptoms and 55% elevated LDH. CHOEP was used in 47% and 34% CHOP, and 47% achieved CR after first line; 16% used transplant as consolidation. No EN, EN1 and EN2 were similar regarding clinical characteristics, except, for stage III/IV (58% vs. 79% vs 96%; p < .0001); IPI 32 (58% vs. 59% vs. 99%; p < .0001); ECOG>1 (58% vs. 92% vs. 99%; p < .0001); BMO involvement (16% vs. 24% vs. 63%%; p
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