TY - JOUR
T1 - Outcome of Stem Cell Transplantation in HTLV-1-Associated North American Adult T-Cell Leukemia/Lymphoma
AU - Bazarbachi, Abdul Hamid
AU - Reef, Daniel
AU - Narvel, Hiba
AU - Patel, Riya
AU - Al Hamed, Rama
AU - Vikash, Sindhu
AU - Neupane, Karun
AU - Atalla, Eleftheria
AU - Thakkar, Astha
AU - Rahman, Shafia
AU - Shah, Urvi
AU - Adrianzen-Herrera, Diego
AU - Quinn, Ryann
AU - Zareef, Sumaira
AU - Rabinovich, Emma
AU - De Castro, Alyssa
AU - Joseph, Felisha
AU - Gillick, Kailyn
AU - Mustafa, Jennat
AU - Khatun, Fariha
AU - Lombardo, Amanda
AU - Townsend-Nugent, Latoya
AU - Abreu, Michelly
AU - Chambers, Nicole
AU - Elkind, Richard
AU - Shi, Yang
AU - Wang, Yanhua
AU - Derman, Olga
AU - Gritsman, Kira
AU - Steidl, Ulrich
AU - Goldfinger, Mendel
AU - Kornblum, Noah
AU - Shastri, Aditi
AU - Mantzaris, Ioannis
AU - Bachier-Rodriguez, Liza
AU - Shah, Nishi
AU - Cooper, Dennis
AU - Verma, Amit
AU - Ye, Bihui Hilda
AU - Janakiram, Murali
AU - Sica, Roberto Alejandro
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/6
Y1 - 2023/6
N2 - Adult T-cell leukemia/lymphoma (ATLL) remains challenging to treat and has dismal outcome. Allogeneic stem-cell transplantation (allo-SCT) has promising results, but data remain scarce. In this single-center retrospective analysis of 100 patients with ATLL from north America (67 acute, 22 lymphomatous), 17 underwent allo-SCT and 5 autologous SCT (ASCT), with a median follow-up of 65 months. Post-transplant 3-years relapse incidence (RI) and non-relapse mortality (NRM) were 51% and 37%, respectively, and 3-year progression-free survival (PFS) and overall survival (OS) were 31% and 35%, respectively. ASCT 1-year RI was 80% compared to 30% in allo-SCT (p = 0.03). After adjusting for immortal-time bias, allo-SCT had significantly improved OS (HR = 0.4, p = 0.01). In exploratory multivariate analysis, patients achieving first complete response and Karnofsky score ≥ 90 had significantly better outcomes, as did Black patients, compared to Hispanics, who had worse outcome. In transplanted patients, 14 died within 2 years, 4 of which ASCT recipients. Our data are the largest ATLL transplant cohort presented to date outside of Japan and Europe. We show that allo-SCT, but not ASCT, is a valid option in select ATLL patients, and can induce long term survival, with 40% of patients alive after more than 5 years.
AB - Adult T-cell leukemia/lymphoma (ATLL) remains challenging to treat and has dismal outcome. Allogeneic stem-cell transplantation (allo-SCT) has promising results, but data remain scarce. In this single-center retrospective analysis of 100 patients with ATLL from north America (67 acute, 22 lymphomatous), 17 underwent allo-SCT and 5 autologous SCT (ASCT), with a median follow-up of 65 months. Post-transplant 3-years relapse incidence (RI) and non-relapse mortality (NRM) were 51% and 37%, respectively, and 3-year progression-free survival (PFS) and overall survival (OS) were 31% and 35%, respectively. ASCT 1-year RI was 80% compared to 30% in allo-SCT (p = 0.03). After adjusting for immortal-time bias, allo-SCT had significantly improved OS (HR = 0.4, p = 0.01). In exploratory multivariate analysis, patients achieving first complete response and Karnofsky score ≥ 90 had significantly better outcomes, as did Black patients, compared to Hispanics, who had worse outcome. In transplanted patients, 14 died within 2 years, 4 of which ASCT recipients. Our data are the largest ATLL transplant cohort presented to date outside of Japan and Europe. We show that allo-SCT, but not ASCT, is a valid option in select ATLL patients, and can induce long term survival, with 40% of patients alive after more than 5 years.
KW - Adult T-cell leukemia/Lymphoma
KW - Allogeneic stem-cell transplantation
KW - Autologous stem-cell transplantation
KW - Black
KW - Hispanic
KW - Human T-cell lymphotropic virus type I
KW - Minority
KW - North American
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U2 - 10.1007/s44228-023-00032-y
DO - 10.1007/s44228-023-00032-y
M3 - Article
AN - SCOPUS:85149862200
SN - 2590-0048
VL - 5
SP - 78
EP - 91
JO - Clinical Hematology International
JF - Clinical Hematology International
IS - 2-3
ER -