Skip to main content
Blood logoLink to Blood
. 2022 Mar 10;139(10):1601. doi: 10.1182/blood.2022015692

Tarlock K, Lamble AJ, Wang Y-C, et al. CEBPA-bZip mutations are associated with favorable prognosis in de novo AML: a report from the Children’s Oncology Group. Blood. 2021;138(13):1137-1147.

PMCID: PMC9211438  PMID: 35266998

In Figure 5 on page 1145, the numbers of patients in the CEBPA+/GATA2+ and CEBPA+/CSF3R+ molecular cohorts are reversed. In Figure 5A and C, the curves should be labeled as 23 patients with CEBPA+/GATA2+ and 13 patients with CEBPA+/CSF3R+. In Figure 5B, the curves should be labeled as 20 patients with CEBPA+/GATA2+ and 13 patients with CEBPA+/CSF3R+. The correct numbers of patients were used for analysis. The corrected Figure 5 is shown below.

Figure 5.

Figure 5.

Outcomes of CEBPA-mutant patients according to co-occurring CSF3R and GATA2 mutational status. (A) EFS of dual CEBPA+/CSF3R+ mutant patients compared with those with dual CEBPA+/GATA2+ and those with a CEBPA+ mutation and neither CSF3R nor GATA2; (B) RR of dual CEBPA+/CSF3R+ mutant patients compared with dual CEBPA+/GATA2+ and patients with a CEBPA+ mutation and neither CSF3R nor GATA2; (C) OS of dual CEBPA+/CSF3R+ mutant patients compared with dual CEBPA+/GATA2+ and patients with a CEBPA+ mutation and neither CSF3R nor GATA2.

The errors have been corrected in the online version of the article.

Supplementary Material

Download PPT

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Download PPT

Articles from Blood are provided here courtesy of The American Society of Hematology

RESOURCES