학술논문

Clinical and Immunologic Characteristics of Non-Hematologic Cancers in Patients with Inborn Errors of Immunity.
Document Type
Article
Source
Cancers. Feb2023, Vol. 15 Issue 3, p764. 10p.
Subject
*BIOMARKERS
*GENETIC disorders
*CELL physiology
*RETROSPECTIVE studies
*CASE-control method
*EARLY detection of cancer
*CANCER patients
*IMMUNOLOGICAL deficiency syndromes
*COMPARATIVE studies
*DISEASE susceptibility
*HEMATOLOGIC malignancies
*DESCRIPTIVE statistics
*RESEARCH funding
*TUMORS
*IMMUNOLOGIC diseases
*CELLULAR immunity
*EDUCATION of physicians' assistants
*IMMUNOTHERAPY
*LONGITUDINAL method
*PHENOTYPES
*DISEASE risk factors
*DISEASE complications
Language
ISSN
2072-6694
Abstract
Simple Summary: Comprehensive studies on non-hematologic tumors in patients with inborn errors of immunity are scarce. Using a well-established registry of patients with long-term follow-up, molecular defects associated with these cancers were reported for the first time among these patients. Using the retrospective data available of this national registry of patients with primary immune defects, we clarified that almost all cancer hallmarks are involved in the development of non-hematologic cancers in patients presenting with non-hematologic cancers. Inborn errors of immunity (IEI) are a heterogeneous group of inherited disorders, and almost 500 genes associated with these disorders have been identified. Defects in IEI genes lead to diverse clinical manifestations including increased susceptibility to recurrent or prolonged infections, immune dysregulation phenotypes (such as severe atopy, allergy, autoimmunity, and uncontrolled inflammation, lymphoproliferation), as well as predisposition to malignancies. Although the majority of IEI patients present hematologic cancers, the characteristics of other types of cancers are not well described in these groups of patients. By investigating 5384 IEI patients registered in the Iranian national registry the clinical and immunologic phenotypes of patients with non-hematologic cancers were compared with other malignant and non-malignant patients. Solid tumors were reported <20% of malignant IEI patients (n = 27/144 patients) and appeared to be very heterogeneous by type and localization as well as molecular defects (mainly due to DNA repair defect resulted from ATM deficiency). The correlation between the type of malignancy and survival status was remarkable as patients with non-hematologic cancers survive higher than IEI patients with hematologic cancers. Our findings showed that different types of malignancy could be associated with specific entities of IEI. Therefore, the education of physicians about the risk of malignancies in IEI is required for personalized treatment and appropriate management of patients. [ABSTRACT FROM AUTHOR]