Skip to main content
JTO Clinical and Research Reports logoLink to JTO Clinical and Research Reports
. 2026 Jul 30;7(9):101058. doi: 10.1016/j.jtocrr.2026.101058

Erratum to ‘Clinical and Immunologic Features of Primary Enteric-Type Thymic Adenocarcinomas: A Rare Variant of a Rare Cancer’ [JTO Clinical and Research Reports 7 (2026) 101019]

Alisa K Sivapiromrat a, Meredith J McAdams a, Renee N Donahue b, Carolina Celades b, Wiem Lassoued b, Hana Bagheri b, Elsa Bahiru a, Shannon Swift a, Christine Feierabend a, Susan Sansone a, Laercio DaSilva a, Eva Szabo a,c, Chen Zhao a, Jeffrey Schlom b, James L Gulley b, Arun Rajan a,∗
PMCID: PMC13488555  PMID: 42621957

The publisher regrets that the following errors occurred in the article, including publication of an incorrect p-value, as follows:

  • 1.

    Statistical Analysis section (Page 3)

  • Descriptive statistics were used for the analysis of clinical data. A Mann-Whitney test was used to calculate differences in peripheral blood immune correlates between two groups of patients. Immune subsets with a potentially biologically relevant difference between histologies and with healthy volunteers were defined as those with p less than 0.05, whereas trends were defined as those with p less than 0.02.

  • 2.

    Results section: Immune Profile, Peripheral Immunome (Page 5)

  • Nevertheless, a deeper analysis of immune cell subsets related to the maturation or function of the parental immune cells revealed higher proportions of PD-1-expressing CD4 + central memory (CM) T cells, PD-1-expressing CD8 + CM T cells, and CD8 + effector memory (EM) T cells in patients with thymic ETAC compared with other subtypes of TETs, but not in comparison with healthy donors (Fig. 1).

The correct statements should be:

  • 1.

    Descriptive statistics were used for the analysis of clinical data. A Mann-Whitney test was used to calculate differences in peripheral blood immune correlates between two groups of patients. Immune subsets with a potentially biologically relevant difference between histologies and with healthy volunteers were defined as those with p less than 0.05, whereas trends were defined as those with p less than 0.2.

  • 2.

    Nevertheless, a deeper analysis of immune cell subsets related to the maturation or function of the parental immune cells revealed higher proportions of PD-1-expressing CD4+ central memory (CM) T cells and PD-1-expressing CD8+ CM and effector memory (EM) T cells in patients with thymic ETAC compared with other subtypes of TETs, but not in comparison with healthy donors (Fig. 1).

The publisher would like to apologise for any inconvenience caused.

DOI of original article: 10.1016/j.jtocrr.2026.101019

∗Corresponding author: Arun Rajan.

email address: rajana@mail.nih.gov


Articles from JTO Clinical and Research Reports are provided here courtesy of Elsevier

RESOURCES