Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Primary Immunodeficiency Diseases Network (PIDNet), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
J Clin Immunol. 2024 Oct 28;45(1):34. doi: 10.1007/s10875-024-01810-w.
Patients with inborn errors of immunity (IEI) are susceptible to developing cancer due to defects in the immune system. The prevalence of cancer is higher in IEI patients compared to the immunocompetent population and cancers are considered as an important and common cause of death in IEI patients.
To systematically review demographic, genetic and cancer-related data of IEI patients with a history of malignancy. Moreover, we performed a meta-analysis aiming to determine the frequency of cancer in patients with different types of IEI.
We conducted electronic searches on Embase, Web of Science, PubMed, and Scopus (until September 2023) introducing terms related to IEI and cancer. Studies with human subjects with confirmed IEI who had developed at least one malignancy during their lifetime were included.
A total number of 4607 IEI patients with a cancer history were included in the present study. Common variable immunodeficiency (CVID) had the highest number of reported cases (1284 cases), mainly due to a higher relative proportion of patients with predominantly antibody deficiencies (PAD) and their increased life expectancy contributing to the higher detection and reporting of cancers among these patients. The most common malignancy was hematologic/blood cancers (3026 cases, mainly diffuse large B cell lymphoma). A total number of 1173 cases (55.6%) succumbed to cancer, with the highest rate of bone marrow failure (64.9%). Among the patients with monogenic defects in IEI-associated genes, the majority of cases had ATM deficiency (926 cases), but the highest cancer frequency rate belonged to NBS1 deficiency (50.5%). 1928 cases out of total 4607 eligible cases had detailed data to allow further statistical analysis that revealed BRCA2 deficiency had the earliest cancer development (~ 38 months), lowest cure frequency, and highest fatality rate (85%), while ATM deficiency had the lowest cure frequency and highest fatality rate (72%) among total cases reviewed with exclusion of Fanconi anemia.
The overall reported cancer frequency in the cases reviewed with and without exclusion of Fanconi anemia was 11.1% (95% confidence interval: 9.8-12.5%) and 12.0% (95% confidence interval: 10.6-13.5%), respectively. Our study revealed that the incidence of cancer is significantly dependent on the molecular and pathway defects in IEI patients, and individualized early screening and appropriate treatment, might improve the prognosis of these patients.
由于免疫系统缺陷,患有先天性免疫缺陷(IEI)的患者易患癌症。与免疫功能正常人群相比,IEI 患者的癌症患病率更高,癌症被认为是 IEI 患者的重要和常见死因。
系统回顾有恶性肿瘤病史的 IEI 患者的人口统计学、遗传学和癌症相关数据。此外,我们进行了荟萃分析,旨在确定不同类型 IEI 患者的癌症发病率。
我们在 Embase、Web of Science、PubMed 和 Scopus 上进行了电子检索(截至 2023 年 9 月),引入了与 IEI 和癌症相关的术语。纳入了有明确 IEI 病史且一生中至少患有一种恶性肿瘤的人类受试者的研究。
本研究共纳入 4607 例有癌症病史的 IEI 患者。常见可变免疫缺陷(CVID)报告的病例数最多(1284 例),主要是由于主要抗体缺陷(PAD)患者的相对比例较高,以及这些患者的预期寿命延长,导致癌症的检测和报告增加。最常见的恶性肿瘤是血液/血液癌症(3026 例,主要是弥漫性大 B 细胞淋巴瘤)。共有 1173 例(55.6%)死于癌症,其中骨髓衰竭(64.9%)的比例最高。在与 IEI 相关基因单基因缺陷的患者中,大多数是 ATM 缺陷(926 例),但癌症发病率最高的是 NBS1 缺陷(50.5%)。在 4607 例符合条件的病例中,有 1928 例有详细数据可进行进一步的统计分析,结果表明 BRCA2 缺陷的癌症发病最早(~38 个月),治愈率最低,死亡率最高(85%),而 ATM 缺陷的治愈率最低,死亡率最高(72%),不包括范可尼贫血。
本研究纳入的病例(包括和不包括范可尼贫血)的总体癌症发病率分别为 11.1%(95%置信区间:9.8-12.5%)和 12.0%(95%置信区间:10.6-13.5%)。我们的研究表明,癌症的发生与 IEI 患者的分子和途径缺陷显著相关,个体化的早期筛查和适当治疗可能改善这些患者的预后。