Prognostic Score and Cytogenetic Risk Classification for Chronic Lymphocytic Leukemia Patients: Center for International Blood and Marrow Transplant Research Report.
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BORIS DOI
Publisher DOI
PubMed ID
31253630
Description
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.
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.
Date of Publication
2019-08-15
Publication Type
Article
Subject(s)
Language(s)
en
Contributor(s)
Kim, Haesook T | |
Ahn, Kwang Woo | |
Hu, Zhen-Huan | |
Davids, Matthew S | |
Volpe, Virginia O | |
Antin, Joseph H | |
Sorror, Mohamed L | |
Shadman, Mazyar | |
Press, Oliver | |
Pidala, Joseph | |
Hogan, William | |
Negrin, Robert | |
Devine, Steven | |
Uberti, Joseph | |
Agura, Edward | |
Nash, Richard | |
Mehta, Jayesh | |
McGuirk, Joseph | |
Forman, Stephen | |
Langston, Amelia | |
Giralt, Sergio A | |
Perales, Miguel-Angel | |
Battiwalla, Minoo | |
Hale, Gregory A | |
Gale, Robert Peter | |
Marks, David I | |
Hamadani, Mehdi | |
Ganguly, Sid | |
Lazarus, Hillard | |
Reshef, Ran | |
Hildebrandt, Gerhard C | |
Inamoto, Yoshihiro | |
Cahn, Jean-Yves | |
Solh, Melhem | |
Kharfan-Dabaja, Mohamed A | |
Ghosh, Nilanjan | |
Saad, Ayman | |
Aljurf, Mahmoud | |
Schouten, Harry C | |
Hill, Brian T | |
Pawarode, Attaphol | |
Kindwall-Keller, Tamila | |
Saba, Nakhle | |
Copelan, Edward A | |
Nathan, Sunita | |
Beitinjaneh, Amer | |
Savani, Bipin N | |
Cerny, Jan | |
Grunwald, Michael R | |
Yared, Jean | |
Wirk, Baldeep M | |
Nishihori, Taiga | |
Chhabra, Saurabh | |
Olsson, Richard F | |
Bashey, Asad | |
Gergis, Usama | |
Popat, Uday | |
Sobecks, Ronald | |
Alyea, Edwin | |
Saber, Wael | |
Brown, Jennifer R |
Additional Credits
Series
Clinical cancer research
Publisher
American Association for Cancer Research
ISSN
1078-0432
Access(Rights)
restricted