Suppr超能文献

伊朗肾母细胞瘤治疗的现状与未来展望

Current status and future perspectives of wilms tumor treatment in Iran.

作者信息

Zahir Mazyar, Alidousti Arash, Kajbafzadeh Abdol-Mohammad, Arshadi Hamid, Kompani Farzad, Hajivalizadeh Sepideh, Zolbin Masoumeh Majidi, Ghohestani Seyed Mohammad, Amirzargar Hossein, Hekmati Pooya

机构信息

Urology and Nephrology Research Center, Shahid Beheshti University of Medical Sciences.

Department of Pediatric Urology, Pediatric Urology and Regenerative Medicine Research Center.

出版信息

Ann Med Surg (Lond). 2023 Apr 18;85(5):1425-1429. doi: 10.1097/MS9.0000000000000671. eCollection 2023 May.

Abstract

UNLABELLED

Wilms tumor (WT) is among the most common pediatric malignancies. In this study, the authors tried to evaluate the adherence to internationally-approved WT treatment protocols in our tertiary medical center in Iran.

METHODS

In this retrospective study, the medical records of 72 pathologically confirmed WT patients who underwent treatment from April 2014 to February 2020 were evaluated. Demographic characteristics, histologic features of the tumors and metastases, utilized treatments, and survival rates were subsequently investigated.

RESULTS

From the total of 72 patients, 31 (43.1%) and 41 (56.9%) were males and females, respectively. The median age at the time of diagnosis was 44.0 (interquartile range: 18.5, 72.0) months. Among the patients, favorable histology was observed in 68 (94.6%) patients, while 4 (5.4%) patients had unfavorable histology. Regarding chemotherapy, 34/56 (60.7%), 4/56 (7.1%), and 18/56 (32.2%) received adjuvant, neoadjuvant, and combined chemotherapy, respectively. The mean numbers of neoadjuvant and adjuvant chemotherapy sessions were 9.4±5.6 and 14.5±11.1, respectively. 32/72 (44.4%) of the patients received adjuvant radiotherapy with a mean number of 7.3±3.6 sessions. Overall survival rates were 86% at 1-year, 74% at 3-year, and 62% at 5-year.

CONCLUSION

Our results suggested that while the demographic characteristics of WT patients in Iran resemble those in other countries, abidance to internationally recommended protocols is relatively low. Moreover, survival rates were rather dismal in our study compared to those from other developing countries, further signifying the need for the development of a nation-specific treatment protocol for WT.

摘要

未标注

肾母细胞瘤(WT)是最常见的儿科恶性肿瘤之一。在本研究中,作者试图评估伊朗一家三级医疗中心对国际认可的WT治疗方案的依从性。

方法

在这项回顾性研究中,对2014年4月至2020年2月期间接受治疗的72例经病理确诊的WT患者的病历进行了评估。随后调查了人口统计学特征、肿瘤和转移灶的组织学特征、采用的治疗方法以及生存率。

结果

在总共72例患者中,男性31例(43.1%),女性41例(56.9%)。诊断时的中位年龄为44.0(四分位间距:18.5,72.0)个月。在患者中,68例(94.6%)观察到良好的组织学,而4例(5.4%)患者组织学不良。关于化疗,56例中有34例(60.7%)、4例(7.1%)和18例(32.2%)分别接受了辅助化疗、新辅助化疗和联合化疗。新辅助化疗和辅助化疗的平均疗程数分别为9.4±5.6和14.5±11.1。72例患者中有32例(44.4%)接受了辅助放疗,平均疗程数为7.3±3.6次。1年总生存率为86%,3年为74%,5年为62%。

结论

我们的结果表明,虽然伊朗WT患者的人口统计学特征与其他国家相似,但对国际推荐方案的依从性相对较低。此外,与其他发展中国家相比,我们研究中的生存率相当低,这进一步表明需要制定针对WT的国家特定治疗方案。

相似文献

1
Current status and future perspectives of wilms tumor treatment in Iran.
Ann Med Surg (Lond). 2023 Apr 18;85(5):1425-1429. doi: 10.1097/MS9.0000000000000671. eCollection 2023 May.
3
Clinical outcomes of children with Wilms tumor treated on a SIOP WT 2001 protocol in a tertiary care hospital in south India.
J Pediatr Urol. 2018 Dec;14(6):547.e1-547.e7. doi: 10.1016/j.jpurol.2018.05.020. Epub 2018 Jun 28.
4
Bilateral Wilms tumors: Treatment results from a single center.
Turk J Pediatr. 2019;61(1):44-51. doi: 10.24953/turkjped.2019.01.008.
5
Wilms' tumor: a 10 year retrospective study.
Arch Iran Med. 2007 Jan;10(1):65-9.
6
Management and outcome of pediatric metastatic Wilms' tumor at the National Cancer Institute, Egypt.
J Egypt Natl Canc Inst. 2020 Apr 15;32(1):19. doi: 10.1186/s43046-020-00031-7.
9
[A long-term follow-up report of pediatric relapsed Wilms tumor after retreatment].
Zhonghua Er Ke Za Zhi. 2017 Oct 2;55(10):743-747. doi: 10.3760/cma.j.issn.0578-1310.2017.10.006.

引用本文的文献

1
Hope and challenges in the diagnosis and treatment of Wilms tumor: a single-center retrospective study in China.
Front Pediatr. 2025 Apr 14;13:1527039. doi: 10.3389/fped.2025.1527039. eCollection 2025.
2
The outcomes of children with primary malignant renal tumors: a 14-year single-center experience.
BMC Cancer. 2024 Nov 12;24(1):1388. doi: 10.1186/s12885-024-13150-4.

本文引用的文献

3
Outcome of Children with Wilms' Tumor in Developing Countries.
J Med Life. 2020 Oct-Dec;13(4):484-489. doi: 10.25122/jml-2019-0084.
4
Incidence of childhood renal tumours: An international population-based study.
Int J Cancer. 2020 Dec 15;147(12):3313-3327. doi: 10.1002/ijc.33147. Epub 2020 Jul 22.
5
Management and outcome of pediatric metastatic Wilms' tumor at the National Cancer Institute, Egypt.
J Egypt Natl Canc Inst. 2020 Apr 15;32(1):19. doi: 10.1186/s43046-020-00031-7.
6
The PROCESS 2018 statement: Updating Consensus Preferred Reporting Of CasE Series in Surgery (PROCESS) guidelines.
Int J Surg. 2018 Dec;60:279-282. doi: 10.1016/j.ijsu.2018.10.031. Epub 2018 Oct 22.
8
Wilms Tumor Treatment Outcomes: Perspectives From a Low-Income Setting.
J Glob Oncol. 2016 Dec 21;3(5):555-562. doi: 10.1200/JGO.2016.005389. eCollection 2017 Oct.
9
Position paper: Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol.
Nat Rev Urol. 2017 Dec;14(12):743-752. doi: 10.1038/nrurol.2017.163. Epub 2017 Oct 31.
10
Bilateral Wilms tumour: a review of clinical and molecular features.
Expert Rev Mol Med. 2017 Jul 18;19:e8. doi: 10.1017/erm.2017.8.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验