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Data from Prognostic Score and Cytogenetic Risk Classification for Chronic Lymphocytic Leukemia Patients: Center for International Blood and Marrow Transplant Research Report

Authors :
Jennifer R. Brown
Wael Saber
Edwin Alyea
Ronald Sobecks
Uday Popat
Usama Gergis
Asad Bashey
Richard F. Olsson
Saurabh Chhabra
Taiga Nishihori
Baldeep M. Wirk
Jean Yared
Michael R. Grunwald
Jan Cerny
Bipin N. Savani
Amer Beitinjaneh
Sunita Nathan
Edward A. Copelan
Nakhle Saba
Tamila Kindwall-Keller
Attaphol Pawarode
Brian T. Hill
Harry C. Schouten
Mahmoud Aljurf
Ayman Saad
Nilanjan Ghosh
Mohamed A. Kharfan-Dabaja
Melhem Solh
Jean-Yves Cahn
Yoshihiro Inamoto
Gerhard C. Hildebrandt
Ran Reshef
Hillard Lazarus
Ulrike Bacher
Sid Ganguly
Mehdi Hamadani
David I. Marks
Robert Peter Gale
Gregory A. Hale
Minoo Battiwalla
Miguel-Angel Perales
Sergio A. Giralt
Amelia Langston
Stephen Forman
Joseph McGuirk
Jayesh Mehta
Richard Nash
Edward Agura
Joseph Uberti
Steven Devine
Robert Negrin
William Hogan
Joseph Pidala
Oliver Press
Mazyar Shadman
Mohamed L. Sorror
Joseph H. Antin
Virginia O. Volpe
Matthew S. Davids
Zhen-Huan Hu
Kwang Woo Ahn
Haesook T. Kim
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

Abstract

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.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....127fb7c195b7ee0941c57be78c2964de