TY - JOUR
T1 - Prognostic score and cytogenetic risk classification for chronic lymphocytic leukemia patients
T2 - Center for International blood and marrow transplant research report
AU - Kim, Haesook T.
AU - Ahn, Kwang Woo
AU - Hu, Zhen Huan
AU - Davids, Matthew S.
AU - Volpe, Virginia O.
AU - Antin, Joseph H.
AU - Sorror, Mohamed L.
AU - Shadman, Mazyar
AU - Press, Oliver
AU - Pidala, Joseph
AU - Hogan, William
AU - Negrin, Robert
AU - Devine, Steven
AU - Uberti, Joseph
AU - Agura, Edward
AU - Nash, Richard
AU - Mehta, Jayesh
AU - McGuirk, Joseph
AU - Forman, Stephen
AU - Langston, Amelia
AU - Giralt, Sergio A.
AU - Perales, Miguel Angel
AU - Battiwalla, Minoo
AU - Hale, Gregory A.
AU - Gale, Robert Peter
AU - Marks, David I.
AU - Hamadani, Mehdi
AU - Ganguly, Sid
AU - Bacher, Ulrike
AU - Lazarus, Hillard
AU - Reshef, Ran
AU - Hildebrandt, Gerhard C.
AU - Inamoto, Yoshihiro
AU - Cahn, Jean Yves
AU - Solh, Melhem
AU - Kharfan-Dabaja, Mohamed A.
AU - Ghosh, Nilanjan
AU - Saad, Ayman
AU - Aljurf, Mahmoud
AU - Schouten, Harry C.
AU - Hill, Brian T.
AU - Pawarode, Attaphol
AU - Kindwall-Keller, Tamila
AU - Saba, Nakhle
AU - Copelan, Edward A.
AU - Nathan, Sunita
AU - Beitinjaneh, Amer
AU - Savani, Bipin N.
AU - Cerny, Jan
AU - Grunwald, Michael R.
AU - Yared, Jean
AU - Wirk, Baldeep M.
AU - Nishihori, Taiga
AU - Chhabra, Saurabh
AU - Olsson, Richard F.
AU - Bashey, Asad
AU - Gergis, Usama
AU - Popat, Uday
AU - Sobecks, Ronald
AU - Alyea, Edwin
AU - Saber, Wael
AU - Brown, Jennifer R.
N1 - Publisher Copyright:
© 2019 American Association for Cancer Research.
PY - 2019/8/15
Y1 - 2019/8/15
N2 - Purpose: To develop a prognostic model and cytogenetic risk classification for previously treated patients with chronic lymphocytic leukemia (CLL) undergoing reduced intensity conditioning (RIC) allogeneic hematopoietic cell transplantation (HCT). Experimental Design: We performed a retrospective analysis of outcomes of 606 patients with CLL who underwent RIC allogeneic HCT between 2008 and 2014 reported to the Center for International Blood and Marrow Transplant Research. Results: On the basis of multivariable models, disease status, comorbidity index, lymphocyte count, and white blood cell count at HCT were selected for the development of prognostic model. Using the prognostic score, we stratified patients into low-, intermediate-, high-, and very-high-risk [4-year progression-free survival (PFS) 58%, 42%, 33%, and 25%, respectively, P < 0.0001; 4-year overall survival (OS) 70%, 57%, 54%, and 38%, respectively, P < 0.0001]. We also evaluated karyotypic abnormalities together with del(17p) and found that del(17p) or 5 abnormalities showed inferior PFS. Using a multivariable model, we classified cytogenetic risk into low, intermediate, and high (P < 0.0001). When the prognostic score and cytogenetic risk were combined, patients with low prognostic score and low cytogenetic risk had prolonged PFS (61% at 4 years) and OS (75% at 4 years). Conclusions: In this large cohort of patients with previously treated CLL who underwent RIC HCT, we developed a robust prognostic scoring system of HCT outcomes and a novel cytogenetic-based risk stratification system. These prognostic models can be used for counseling patients, comparing data across studies, and providing a benchmark for future interventions. For future study, we will further validate these models for patients receiving targeted therapies prior to HCT.
AB - Purpose: To develop a prognostic model and cytogenetic risk classification for previously treated patients with chronic lymphocytic leukemia (CLL) undergoing reduced intensity conditioning (RIC) allogeneic hematopoietic cell transplantation (HCT). Experimental Design: We performed a retrospective analysis of outcomes of 606 patients with CLL who underwent RIC allogeneic HCT between 2008 and 2014 reported to the Center for International Blood and Marrow Transplant Research. Results: On the basis of multivariable models, disease status, comorbidity index, lymphocyte count, and white blood cell count at HCT were selected for the development of prognostic model. Using the prognostic score, we stratified patients into low-, intermediate-, high-, and very-high-risk [4-year progression-free survival (PFS) 58%, 42%, 33%, and 25%, respectively, P < 0.0001; 4-year overall survival (OS) 70%, 57%, 54%, and 38%, respectively, P < 0.0001]. We also evaluated karyotypic abnormalities together with del(17p) and found that del(17p) or 5 abnormalities showed inferior PFS. Using a multivariable model, we classified cytogenetic risk into low, intermediate, and high (P < 0.0001). When the prognostic score and cytogenetic risk were combined, patients with low prognostic score and low cytogenetic risk had prolonged PFS (61% at 4 years) and OS (75% at 4 years). Conclusions: In this large cohort of patients with previously treated CLL who underwent RIC HCT, we developed a robust prognostic scoring system of HCT outcomes and a novel cytogenetic-based risk stratification system. These prognostic models can be used for counseling patients, comparing data across studies, and providing a benchmark for future interventions. For future study, we will further validate these models for patients receiving targeted therapies prior to HCT.
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U2 - 10.1158/1078-0432.CCR-18-3988
DO - 10.1158/1078-0432.CCR-18-3988
M3 - Article
C2 - 31253630
AN - SCOPUS:85070674030
SN - 1078-0432
VL - 25
SP - 5143
EP - 5155
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 16
ER -