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ABSTRACT: Background
The role of allogeneic hematopoietic cell transplantation (alloHCT) in acute myeloid leukemia (AML) with mutated IDH1/2 has not been defined. Therefore, we analyzed a large cohort of 3234 AML patients in first complete remission (CR1) undergoing alloHCT or conventional chemo-consolidation and investigated outcome in respect to IDH1/2 mutational subgroups (IDH1 R132C, R132H and IDH2 R140Q, R172K).Methods
Genomic DNA was extracted from bone marrow or peripheral blood samples at diagnosis and analyzed for IDH mutations with denaturing high-performance liquid chromatography, Sanger sequencing and targeted myeloid panel next-generation sequencing, respectively. Statistical as-treated analyses were performed using R and standard statistical methods (Kruskal-Wallis test for continuous variables, Chi-square test for categorical variables, Cox regression for univariate and multivariable models), incorporating alloHCT as a time-dependent covariate.Results
Among 3234 patients achieving CR1, 7.8% harbored IDH1 mutations (36% R132C and 47% R132H) and 10.9% carried IDH2 mutations (77% R140Q and 19% R172K). 852 patients underwent alloHCT in CR1. Within the alloHCT group, 6.2% had an IDH1 mutation (43.4% R132C and 41.4% R132H) and 10% were characterized by an IDH2 mutation (71.8% R140Q and 24.7% R172K). Variants IDH1 R132C and IDH2 R172K showed a significant benefit from alloHCT for OS (p = .017 and p = .049) and RFS (HR = 0.42, p = .048 and p = .009) compared with chemotherapy only. AlloHCT in IDH2 R140Q mutated AML resulted in longer RFS (HR = 0.4, p = .002).Conclusion
In this large as-treated analysis, we showed that alloHCT is able to overcome the negative prognostic impact of certain IDH mutational subclasses in first-line consolidation treatment and could pending prognostic validation, provide prognostic value for AML risk stratification and therapeutic decision making.
SUBMITTER: Kunadt D
PROVIDER: S-EPMC9442956 | biostudies-literature | 2022 Sep
REPOSITORIES: biostudies-literature
Kunadt Desiree D Stasik Sebastian S Metzeler Klaus H KH Röllig Christoph C Schliemann Christoph C Greif Philipp A PA Spiekermann Karsten K Rothenberg-Thurley Maja M Krug Utz U Braess Jan J Krämer Alwin A Hochhaus Andreas A Scholl Sebastian S Hilgendorf Inken I Brümmendorf Tim H TH Jost Edgar E Steffen Björn B Bug Gesine G Einsele Hermann H Görlich Dennis D Sauerland Cristina C Schäfer-Eckart Kerstin K Krause Stefan W SW Hänel Mathias M Hanoun Maher M Kaufmann Martin M Wörmann Bernhard B Kramer Michael M Sockel Katja K Egger-Heidrich Katharina K Herold Tobias T Ehninger Gerhard G Burchert Andreas A Platzbecker Uwe U Berdel Wolfgang E WE Müller-Tidow Carsten C Hiddemann Wolfgang W Serve Hubert H Stelljes Matthias M Baldus Claudia D CD Neubauer Andreas A Schetelig Johannes J Thiede Christian C Bornhäuser Martin M Middeke Jan M JM Stölzel Friedrich F
Journal of hematology & oncology 20220905 1
<h4>Background</h4>The role of allogeneic hematopoietic cell transplantation (alloHCT) in acute myeloid leukemia (AML) with mutated IDH1/2 has not been defined. Therefore, we analyzed a large cohort of 3234 AML patients in first complete remission (CR1) undergoing alloHCT or conventional chemo-consolidation and investigated outcome in respect to IDH1/2 mutational subgroups (IDH1 R132C, R132H and IDH2 R140Q, R172K).<h4>Methods</h4>Genomic DNA was extracted from bone marrow or peripheral blood sam ...[more]