对 84 名摩洛哥患者的 Wilms 肿瘤流行病学、临床病理特征和治疗结果进行分析。

IF 1.5 Q4 ONCOLOGY
Cancer reports Pub Date : 2024-11-01 DOI:10.1002/cnr2.2158
Sara Benlhachemi, Mohammed Khattab, Kenza Hattoufi, Redouane Abouqal, Saber Boutayeb, Elmostafa El Fahime
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引用次数: 0

摘要

背景介绍Wilms瘤(WT)是摩洛哥报告的第二大儿童癌症,是一种影响15岁以下儿童的恶性肾肿瘤。随着多模式治疗的采用,预后有所改善。目的:本研究旨在全面描述和分析摩洛哥 WT 患者的流行病学、临床病理特征和治疗效果,包括治疗反应和复发率:2014年1月至2018年2月期间,84名15岁以下的WT患儿在拉巴特儿童医院儿科血液学和肿瘤学中心接受了SIOP方案治疗和随访。参与者的中位年龄为 36 个月,男女性别比为 0.79。55例(66%)患者的主要病症为腹部肿块。5例患者(6%)为双侧WT。21例(25%)发生转移性WT。33例(43%)患者以III期为主。20例(26%)为高危WT,12例(14%)观察到IVC瘤栓。WT 组织类型与性别和肿瘤定位有明显相关性(P 值分别为 0.040 和 0.013)。年龄与 WT 扩展、总体分期和 SIOP 组织学风险分级有明显相关性(p 值分别为 0.003、0.003 和 0.045)。总体分期与 IVC 肿瘤血栓的发生有统计学关系(p = 0.002)。在肾切除术后的5年时间里,63名患者(75%)的病情得到完全缓解,1名患者(1%)的病情得到部分缓解,19名患者(23%)死亡,1名患者(1%)复发:对于一个发展中国家来说,这些研究结果令人鼓舞。然而,该系列研究中 III 期和 IVC 血栓的发病率仍然很高,这主要归因于诊断和治疗的延误,以及研究时儿科血液学和肿瘤学单位的数量有限。尽管如此,仍有必要进一步开展多中心研究,以丰富摩洛哥的数据,并建立全国 WT 病例登记册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of Wilms Tumour Epidemiology, Clinicopathological Features and Treatment Outcomes in 84 Moroccan Patients.

Background: Wilms tumour (WT), the second most reported childhood cancer in Morocco, is a malignant kidney tumour that affects children under 15 years old. Prognosis has improved with the adoption of multimodal treatment. However, data on WT in Morocco remain limited.

Aims: This study aims to comprehensively describe and analyse the epidemiological, clinicopathological features and treatment outcomes of WT in Moroccan patients, including treatment response and recurrence rates.

Methods and results: A retrospective study involved 84 children under 15 years with WT, treated according to the SIOP protocol and followed at the Paediatric Haematology and Oncology Centre at Children's hospital of Rabat, between January 2014 and February 2018. The median age of participants was 36 months, with a male/female sex ratio of 0.79. Abdominal mass was the primary concern in 55 cases (66%). Five patients (6%) had bilateral WT. Metastatic WT occurred in 21 cases (25%). Stage III was predominant in 33 cases (43%). Twenty cases (26%) had high-risk WT, and IVC tumour thrombus was observed in 12 cases (14%). WT histotype correlated significantly with both sex and tumour localisation (p values of 0.040 and 0.013, respectively). Age correlated significantly with WT extension, overall stage and SIOP histology risk grades (p values of 0.003, 0.003 and 0.045, respectively). Overall stage was statistically related to the occurrence of IVC tumour thrombus (p = 0.002). Over a 5-year span post-nephrectomy, complete remission was achieved in 63 patients (75%), partial remission in one patient (1%), while 19 patients (23%) died and one patient (1%) relapsed.

Conclusion: These findings are encouraging for a developing country. However, the elevated rates of Stages III and IVC thrombus in this series are still high, primarily attributed to delays in diagnosis and treatment and the limited number of paediatric haematology and oncology units at the time of the study. Nevertheless, further multicentric research is warranted to enrich Moroccan data and establish a national register for WT cases.

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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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