Mutational profile, outcomes, and impact of allogeneic hematopoietic stem cell transplantation in adult patients with acute myeloid leukemia and inconclusive cytogenetic analysis

Author:

Vasudevan Nampoothiri Ram1,Tang Kenny2,Schuh Andre2,Lam Wilson3,Maze Dawn2,Michelis Fotios V.3ORCID,Chan Steven2,Gupta Vikas2,Kim Dennis3ORCID,Kumar Rajat3,Lipton Jeffrey Howard3ORCID,Mattsson Jonas3,Minden Mark2,Schimmer Aaron2,Sibai Hassan2,Viswabandya Auro3,Yee Karen2,Murphy Tracy2,Law Arjun D.3

Affiliation:

1. The Ottawa Hospital Bone Marrow Transplant Programme University of Ottawa Ottawa Ontario Canada

2. Leukemia Program Princess Margaret Cancer Centre, University of Toronto Toronto Ontario Canada

3. Hans Messner Allogeneic Blood and Marrow Transplant Program Princess Margaret Cancer Centre, University of Toronto Toronto Ontario Canada

Abstract

AbstractBackgroundInconclusive cytogenetic analysis (IC) at baseline has been reported as a predictor of poor prognosis in patients with acute myeloid leukemia (AML). The mutational profile in this group of patients, and its impact on outcomes have not been reported.MethodsWe retrospectively analyzed adult patients (≥18 years) with newly diagnosed AML treated with intensive induction chemotherapy between 2015 and 2019. Patients with any documented cytogenetic abnormalities were excluded. Targeted next generation sequencing (NGS) was performed in all patients. Baseline characteristics, mutation profile, and outcomes were compared between patients with normal cytogenetics(NC) and those with IC.ResultsSixty‐one patients (males 39.3%; median age 59 years) had IC at diagnosis. The proportion of patients with mutations in genes with proven prognostic impact were not different between AML patients with IC and NC. AML patients with NC were more likely to harbor the prognostically favorable NPM1mut/FLT3‐ITDwt mutational combination conferring “favorable” risk status. As a result, a larger proportion of patients in the IC group underwent allogeneic hematopoietic stem cell transplantation (allo HCT; 54.1% vs. 39.6%; p = .02). The 2‐year RFS (55.9% vs. 58.5%; p = .29) and OS (61.9% vs. 66.9%; p = .48) were similar in IC and NC patients. There was no difference in survival of patients who underwent allo HCT when compared with patients who did not (p = .99).ConclusionsInconclusive cytogenetic analysis may not be an independent prognostic indicator in AML. In such patients, molecular abnormalities detected through NGS or whole genome sequencing are more likely to be informative.

Publisher

Wiley

Subject

Hematology,General Medicine

Reference18 articles.

1. Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group study

2. The Importance of Diagnostic Cytogenetics on Outcome in AML: Analysis of 1,612 Patients Entered Into the MRC AML 10 Trial

3. Karyotype in acute myeloblastic leukemia: prognostic significance for bone marrow transplantation in first remission: a European Group for Blood and Marrow Transplantation study. Acute Leukemia Working Party of the European Group for Blood and Marrow Transplantation (EBMT);Ferrant A;Blood,1997

4. Impact of cytogenetic abnormalities on outcome of bone marrow transplants in acute myelogenous leukemia in first remission;Gale RP;Bone Marrow Transplant,1995

5. Pre-analytical parameters associated with unsuccessful karyotyping in myeloid neoplasm: a study of 421 samples

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