| Literature DB >> 32781289 |
Aziz Nazha1, Zhen-Huan Hu2, Tao Wang3, R Coleman Lindsley4, Hisham Abdel-Azim5, Mahmoud Aljurf6, Ulrike Bacher7, Asad Bashey8, Jean-Yves Cahn9, Jan Cerny10, Edward Copelan11, Zachariah DeFilipp12, Miguel Angel Diaz13, Nosha Farhadfar14, Shahinaz M Gadalla15, Robert Peter Gale16, Biju George17, Usama Gergis18, Michael R Grunwald11, Betty Hamilton19, Shahrukh Hashmi20, Gerhard C Hildebrandt21, Yoshihiro Inamoto22, Matt Kalaycio23, Rammurti T Kamble24, Mohamed A Kharfan-Dabaja25, Hillard M Lazarus26, Jane L Liesveld27, Mark R Litzow28, Navneet S Majhail19, Hemant S Murthy25, Sunita Nathan29, Taiga Nishihori30, Attaphol Pawarode31, David Rizzieri32, Mitchell Sabloff33, Bipin N Savani34, Levanto Schachter35, Harry C Schouten36, Sachiko Seo37, Nirav N Shah38, Melhem Solh39, David Valcárcel40, Ravi Vij41, Erica Warlick42, Baldeep Wirk43, William A Wood44, Jean A Yared45, Edwin Alyea46, Uday Popat47, Ronald M Sobecks23, Bart L Scott48, Ryotaro Nakamura49, Wael Saber2.
Abstract
Allogeneic hematopoietic stem cell transplantation (HCT) remains the only potentially curative option for myelodysplastic syndromes (MDS). Mortality after HCT is high, with deaths related to relapse or transplant-related complications. Thus, identifying patients who may or may not benefit from HCT is clinically important. We identified 1514 patients with MDS enrolled in the Center for International Blood and Marrow Transplant Research Registry and had their peripheral blood samples sequenced for the presence of 129 commonly mutated genes in myeloid malignancies. A random survival forest algorithm was used to build the model, and the accuracy of the proposed model was assessed by concordance index. The median age of the entire cohort was 59 years. The most commonly mutated genes were ASXL1(20%), TP53 (19%), DNMT3A (15%), and TET2 (12%). The algorithm identified the following variables prior to HCT that impacted overall survival: age, TP53 mutations, absolute neutrophils count, cytogenetics per International Prognostic Scoring System-Revised, Karnofsky performance status, conditioning regimen, donor age, WBC count, hemoglobin, diagnosis of therapy-related MDS, peripheral blast percentage, mutations in RAS pathway, JAK2 mutation, number of mutations/sample, ZRSR2, and CUX1 mutations. Different variables impacted the risk of relapse post-transplant. The new model can provide survival probability at different time points that are specific (personalized) for a given patient based on the clinical and mutational variables that are listed above. The outcomes' probability at different time points may aid physicians and patients in their decision regarding HCT.Entities:
Keywords: Genomic biomarkers; MDS; Mutations
Mesh:
Year: 2020 PMID: 32781289 PMCID: PMC7609542 DOI: 10.1016/j.bbmt.2020.08.003
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742