Profile and Clinical Outcome of Children with Wilms' Tumor treated at a Tertiary Care Centre, India.

IF 0.6 Q4 ONCOLOGY South Asian Journal of Cancer Pub Date : 2022-07-01 DOI:10.1055/s-0042-1743414
Pritanjali Singh, Dharmendra Singh, Bindey Kumar, Prem Kumar, Punam Prasad Bhadani
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Abstract

Pritanjali SinghBackground  Wilms' tumor (WT) is the most common kidney tumor of the pediatric age group. The outcome of WT has improved due to the evolution of the treatment approach. A prospective observational study was conducted at All India Institute of Medical Sciences (AIIMS), Patna, to analyze the clinical profile along with the response and outcome to neoadjuvant chemotherapy according to the International Society of Pediatric Oncology (SIOP) protocol. Materials and Methods  In total, 28 patients of WT visited the radiotherapy department from January 2015 to December 2019. Results  Gender distribution showed male preponderance with a median age at diagnosis was 31 months. The abdominal lump was the dominant clinical presentation. The median volume of tumor at diagnosis was 359.48 mL (52.67-1805.76). Radiological staging workup shows that stage I, II, III, IV, and V were 7.1%, 39.3%, 39.3%, 10.7%, and 3.6% respectively. Neoadjuvant chemotherapy (NACT) was received by all patients. Also, 71.4% of patients showed > 50% of tumor volume reduction, while 28.6% of patients showed < 50% of tumor mass reduction. There was a statistically significant decrease in the tumor volume reduction following neoadjuvant chemotherapy ( p  < 0.001). There was a statistically significant stage down ( p  = 0.018) of the disease. Bivariate correlation studies showed recurrence was correlating statistically significantly with age < 24 months ( p  = 0.049), locoregional lymph nodes ( p  = 0.008), histopathological subtypes ( p  < 0.001), stage of the disease ( p  = 0.003), and risk groups ( p  < 0.001). In addition, 25% of patients developed recurrence during the median follow-up of 25 months. The median disease-free survival (DFS) and overall survival (OS) were not reached. The mean DFS and OS were 48 and 59.13 months, respectively. One- and 3-year DFS were 100% and 64.1%, respectively. One- and 3-year OS were 100% and 75% respectively. Conclusion  Our study suggests that most of the patients presented at an advanced stage, thus rendering most of the cases difficult to undergo surgery at presentation. Neoadjuvant chemotherapy followed by surgery may be considered a well-balanced approach with a comparable response and survival outcomes.

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在印度三级保健中心治疗的儿童Wilms肿瘤的概况和临床结果。
肾母细胞瘤(Wilms' tumor, WT)是儿童年龄段最常见的肾脏肿瘤。由于治疗方法的发展,WT的结果得到了改善。在巴特那全印度医学科学研究所(AIIMS)进行了一项前瞻性观察研究,根据国际儿科肿瘤学会(SIOP)协议,分析临床概况以及对新辅助化疗的反应和结果。材料与方法2015年1月至2019年12月放疗科共收治WT患者28例。结果性别分布以男性为主,诊断时中位年龄为31个月。腹部肿块是主要的临床表现。诊断时肿瘤中位体积为359.48 mL(52.67 ~ 1805.76)。放射分期检查显示,I期、II期、III期、IV期和V期分别为7.1%、39.3%、39.3%、10.7%和3.6%。所有患者均接受新辅助化疗(NACT)。71.4%的患者肿瘤体积缩小> 50%,28.6%的患者肿瘤体积缩小(p = 0.018)。双变量相关研究显示,复发与年龄(p = 0.049)、局部区域淋巴结(p = 0.008)、组织病理学亚型(p = 0.003)和危险组(p)有统计学意义上的相关。结论我们的研究表明,大多数患者出现在晚期,因此大多数病例难以在就诊时进行手术。手术后的新辅助化疗可能被认为是一种平衡的方法,具有相当的反应和生存结果。
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CiteScore
1.00
自引率
0.00%
发文量
80
审稿时长
35 weeks
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