Bhuko Jeffer O, Tebuka Erius, Ottoman Oscar, Schroeder Kristin
Pathology Department, School of Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania.
Oncology Department, Bugando Medical Centre, Mwanza, Tanzania.
Ecancermedicalscience. 2024 Dec 5;18:1809. doi: 10.3332/ecancer.2024.1809. eCollection 2024.
In nations with poor and intermediate incomes, cancer is one of the main causes of mortality. Immunohistochemistry (IHC) is crucial for an accurate cancer evaluation, prognosis and treatment decision-making. To use IHC, a significant amount of facilities and capacity growth are needed. Because of this, it is crucial to comprehend the potential effects of IHC and identify the most essential reagents required to distinguish between typical diagnoses in our environment.
Employing IHC, this study aims to assess how well paediatric cancer diagnoses in Tanzania can be made and to identify the most widely used biomarkers for diagnostic distinction.
Pathology samples from kids who were given cancer diagnoses in 2018 at the Bugando Medical Centre in Mwanza, Tanzania, were examined using H&E staining. Basic demographic information from the histology form was gathered in addition to the reported histopathology results from Bugando Medical Centre, including patient age, sex and sample collection. Muhimbili National Hospital received tissue from the histology block for the IHC examination. It was determined which reagents/biomarkers were required for diagnostic confirmation by comparing the histopathology data for diagnostic agreement, variations in diagnosis and other factors.
The examinations included 105 (105) patients with paediatric cancer. 55.2% of the population, who had a median age of 6 years (IQR 3-9), were female. Burkitt and NHL-DLBCL were the paediatric diagnoses with the greatest pathology. The correlation between H&E and IHC histology was 51.0%. 17.6% ( = 18) of diagnoses had enhanced diagnostic specificity (e.g., NHL to diffuse large B cell lymphoma), and 31.4% of diagnoses were altered as a result of IHC.
Considering that the diagnosis of juvenile cancer changes in about 30% of cases, IHC is crucial for accurate diagnosis. IHC retraining is crucial, and developing nations can successfully adopt a modest shared biomarker panel to improve therapy allocation.
在中低收入国家,癌症是主要死因之一。免疫组织化学(IHC)对于准确的癌症评估、预后及治疗决策至关重要。要开展免疫组织化学检测,需要大量设施及能力建设。因此,了解免疫组织化学的潜在影响并确定在我们的环境中区分典型诊断所需的最重要试剂至关重要。
本研究旨在通过免疫组织化学评估坦桑尼亚儿童癌症诊断的准确性,并确定用于诊断区分的最常用生物标志物。
对2018年在坦桑尼亚姆万扎布甘多医疗中心被诊断为癌症的儿童的病理样本进行苏木精-伊红(H&E)染色检查。除了布甘多医疗中心报告的组织病理学结果外,还收集了组织学表格中的基本人口统计学信息,包括患者年龄、性别和样本采集情况。穆希姆比利国家医院从组织学切片块中获取组织进行免疫组织化学检查。通过比较诊断一致性、诊断差异及其他因素的组织病理学数据,确定诊断确认所需的试剂/生物标志物。
检查包括105例儿童癌症患者。其中55.2%为女性,中位年龄为6岁(四分位间距3 - 9岁)。伯基特淋巴瘤和非霍奇金淋巴瘤-弥漫性大B细胞淋巴瘤是病理诊断最多的儿童疾病。H&E与免疫组织化学组织学之间的相关性为51.0%。17.6%(n = 18)的诊断提高了诊断特异性(如非霍奇金淋巴瘤诊断为弥漫性大B细胞淋巴瘤),31.4%的诊断因免疫组织化学而改变。
考虑到约30%的青少年癌症诊断会发生变化,免疫组织化学对于准确诊断至关重要。免疫组织化学再培训至关重要,发展中国家可以成功采用适度共享的生物标志物组合来改善治疗分配。