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Outcomes of Allogeneic Hematopoietic Cell Transplantation in T Cell Prolymphocytic Leukemia: A Contemporary Analysis from the Center for International Blood and Marrow Transplant Research.


ABSTRACT: T cell prolymphocytic leukemia (T-PLL) is a rare, aggressive malignancy with limited treatment options and poor long-term survival. Previous studies of allogeneic hematopoietic cell transplantation (alloHCT) for T-PLL are limited by small numbers, and descriptions of patient and transplantation characteristics and outcomes after alloHCT are sparse. In this study, we evaluated outcomes of alloHCT in patients with T-PLL and attempted to identify predictors of post-transplantation relapse and survival. We conducted an analysis of data using the Center for International Blood and Marrow Transplant Research database on 266 patients with T-PLL who underwent alloHCT between 2008 and 2018. The 4-year rates of overall survival (OS), disease-free survival (DFS), relapse, and treatment-related mortality (TRM) were 30.0% (95% confidence interval [CI], 23.8% to 36.5%), 25.7% (95% CI, 20% to 32%), 41.9% (95% CI, 35.5% to 48.4%), and 32.4% (95% CI, 26.4% to 38.6%), respectively. In multivariable analyses, 3 variables were associated with inferior OS: receipt of a myeloablative conditioning (MAC) regimen (hazard ratio [HR], 2.18; P < .0001), age >60 years (HR, 1.61; P = .0053), and suboptimal performance status, defined by Karnofsky Performance Status (KPS) <90 (HR, 1.53; P = .0073). Receipt of an MAC regimen also was associated with increased TRM (HR, 3.31; P < .0001), an elevated cumulative incidence of grade II-IV acute graft-versus-host disease (HR, 2.94; P = .0011), and inferior DFS (HR, 1.86; P = .0004). Conditioning intensity was not associated with relapse; however, stable disease/progression was correlated with increased risk of relapse (HR, 2.13; P = .0072). Both in vivo T cell depletion (TCD) as part of conditioning and KPS <90 were associated with worse TRM and inferior DFS. Receipt of total body irradiation had no significant effect on OS, DFS, or TRM. Our data show that reduced-intensity conditioning without in vivo TCD (ie, without antithymocyte globulin or alemtuzumab) before alloHCT was associated with long-term DFS in patients with T-PLL who were age ≤60 years or who had a KPS >90 or chemosensitive disease.

SUBMITTER: Murthy HS 

PROVIDER: S-EPMC8977261 | biostudies-literature | 2022 Apr

REPOSITORIES: biostudies-literature

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Outcomes of Allogeneic Hematopoietic Cell Transplantation in T Cell Prolymphocytic Leukemia: A Contemporary Analysis from the Center for International Blood and Marrow Transplant Research.

Murthy Hemant S HS   Ahn Kwang Woo KW   Estrada-Merly Noel N   Alkhateeb Hassan B HB   Bal Susan S   Kharfan-Dabaja Mohamed A MA   Dholaria Bhagirathbhai B   Foss Francine F   Gowda Lohith L   Jagadeesh Deepa D   Sauter Craig C   Abid Muhammad Bilal MB   Aljurf Mahmoud M   Awan Farrukh T FT   Bacher Ulrike U   Badawy Sherif M SM   Battiwalla Minoo M   Bredeson Chris C   Cerny Jan J   Chhabra Saurabh S   Deol Abhinav A   Diaz Miguel Angel MA   Farhadfar Nosha N   Freytes César C   Gajewski James J   Gandhi Manish J MJ   Ganguly Siddhartha S   Grunwald Michael R MR   Halter Joerg J   Hashmi Shahrukh S   Hildebrandt Gerhard C GC   Inamoto Yoshihiro Y   Jimenez-Jimenez Antonio Martin AM   Kalaycio Matt M   Kamble Rammurti R   Krem Maxwell M MM   Lazarus Hillard M HM   Lazaryan Aleksandr A   Maakaron Joseph J   Munshi Pashna N PN   Munker Reinhold R   Nazha Aziz A   Nishihori Taiga T   Oluwole Olalekan O OO   Ortí Guillermo G   Pan Dorothy C DC   Patel Sagar S SS   Pawarode Attaphol A   Rizzieri David D   Saba Nakhle S NS   Savani Bipin B   Seo Sachiko S   Ustun Celalettin C   van der Poel Marjolein M   Verdonck Leo F LF   Wagner John L JL   Wirk Baldeep B   Oran Betul B   Nakamura Ryotaro R   Scott Bart B   Saber Wael W  

Transplantation and cellular therapy 20220123 4


T cell prolymphocytic leukemia (T-PLL) is a rare, aggressive malignancy with limited treatment options and poor long-term survival. Previous studies of allogeneic hematopoietic cell transplantation (alloHCT) for T-PLL are limited by small numbers, and descriptions of patient and transplantation characteristics and outcomes after alloHCT are sparse. In this study, we evaluated outcomes of alloHCT in patients with T-PLL and attempted to identify predictors of post-transplantation relapse and survi  ...[more]

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