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Vol. 44. Issue S1.
Pages S30 (October 2022)
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Vol. 44. Issue S1.
Pages S30 (October 2022)
LYMPHOMAPP 07
Open Access
PREVENTION CAN BE THE BEST TOOL FOR ADULT T-CELL LEUKEMIA. UPDATED T-CELL BRAZIL PROJECT
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Carmino De Sousa1, Carlos Chiattone2, Eliana Miranda1, Yung Gonzaga3, Maria Dias4, Renata L R Baptista5, Davimar Borducchi6, Guilherme Duffles1, Marcelo Bellesso7, Juliana Pereira8, Sergio Brasil9, Nelson S CASTRO10, Karin Z CECYN11, Rony SCHAFFEL12, Massimo Federico13
1 University of Campinas – UNICAMP, Hematology and Hemotherapy Center, SP
2 Samaritano Hospital – Higienopolis & Santa Casa Medical School of Sao Paulo
3 Cancer National Institute – INCA, RJ
4 Federal University of Bahia – UFBA
5 State University of Rio de Janeiro – UERJ & Instituto D'Or de Pesquisa e Ensino (IDOR), RJ
6 Medical School of ABC, Santo Andre, SP
7 HemoMed, Instituto de Ensino e Pesquisa – IEP, São Lucas, SP
8 Medicine School of University of São Paulo, SP
9 Santa Casa Medical School of Sao Paulo
10 Cancer Hospital Barretos, Hospital de Amor, SP
11 Federal University of Sao Paulo - UNIFESP
12 Federal University of Rio de Janeiro – UFRJ, Clementino Fraga Hospital, RJ
13 University of Modena and Reggio Emília, Italy
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Objective

T-cell Brazil project started in April 2017 an ambispective study focusing to collecting epidemiological and clinical data from the most frequent subtypes of PTCL, among them the ATL. As of July 2022 T-cell Brazil database contained 81 (16%) ATL out of 520 registered cases. Our goals are to describe demographic and clinical features, analyze the overall and progression-free survival (OS and PFS), and try to identify factors that could influence outcome.

Methodology

Brazilian Registry using REDcap Platform by Vanderbilt realized descriptive and bivariate analyses, then it was applied Kaplan-Meier method and log-rank test to obtain survival estimates, and besides that, it was used the Cox Regression to identify any factor that could influence the OS and PFS.

Results

The median age was 52 years (24-91); 32 (39%) male; the majority of clinical subtypes were 52% lymphoma type; 81% received chemotherapy. The best response assessment after first-line treatment was: progression or no response in 31%; 26% complete response; 21% partial response, 21% not available (NA) due to death or on treatment; 34% of patients were alive and the 24-month OS and PFS was 33% and 21%, respectively. As predictors for PFS and OS were B symptom and elevated LDH values.

Conclusion

This study, even recognizing a limited sample size, highlights the poor prognosis associated with ATL, mainly acute and lymphoma type, with high mortality rates. Hence, apparently, a good shot, it would be one of the bases for the prevention of ATL to establish a disease entity of “chronic active HTLV-1 infection” that defines high-risk carriers for ATL development, and then, enables preventive intervention.

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Idiomas
Hematology, Transfusion and Cell Therapy
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