Long-Term Survey of Japanese Children with Recurrent Nephroblastoma: A Report from Japan Children's Cancer Group.

IF 1.2 4区 医学 Q4 HEMATOLOGY Pediatric Hematology and Oncology Pub Date : 2024-11-05 DOI:10.1080/08880018.2024.2423207
Hiroshi Yagasaki, Yoshiki Katsumi, Miwako Nozaki, Satoshi Hamanoue, Hiroaki Fukuzawa, Koji Fukumoto, Shinji Mochizuki, Shuichiro Uehara, Takaharu Oue, Tsugumichi Koshinaga
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Abstract

In prospective Japanese studies of pediatric renal tumors, 5-year event-free survival and overall survival (OS) for patients with nephroblastoma ranges from 75-90% and 89-97%, respectively. However, treatments strategies for recurrent nephroblastoma in Japanese patients remain unclear. This retrospective study aimed to inform the development of treatment strategies by analyzing the long-term results and side effects of salvage therapies for recurrent nephroblastoma in Japan. A questionnaire survey involving 41 institutions (74 patients) collected clinical data on recurrent cases reported to the Renal Tumor Committee of the Japan Children's Cancer Group. Survey forms from 54 cases were evaluated. Median time to recurrence was 9.5 months among 51 patients without underlying disorders. Recurrence occurred at lung-only in 18 patients and at other sites in 33. The 5-year OS for all 51 patients was 70.6%, with recurrent disease causing death in 15 patients and one patient dying from treatment-related complications. Patients with lung-only recurrence had higher 5-year OS rates than those with other-site recurrence. Initial chemotherapy intensity also affected prognosis, with lower intensity associated with higher 5-year OS. In 17 survivors with lung-only recurrence, the most frequent treatment approach combined chemotherapy, surgery and radiotherapy. Conventional chemotherapy included platinum-containing regimens and/or Regimen I-based treatment containing cyclophosphamide and etoposide. Salvage therapies showed remarkable effectiveness for patients with lung-only recurrence or low intensity of the initial chemotherapy, highlighting the need to standardize prospective studies for post-recurrence treatment and identify risks of late complications for long-term survivors.

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日本复发性肾母细胞瘤患儿的长期调查:日本儿童癌症小组的报告。
在日本对小儿肾脏肿瘤的前瞻性研究中,肾母细胞瘤患者的5年无事件生存率和总生存率(OS)分别为75%-90%和89%-97%。然而,日本患者复发性肾母细胞瘤的治疗策略仍不明确。这项回顾性研究旨在通过分析日本复发性肾母细胞瘤挽救疗法的长期效果和副作用,为治疗策略的制定提供参考。41家医疗机构(74名患者)参与的问卷调查收集了向日本儿童癌症小组肾肿瘤委员会报告的复发病例的临床数据。对54例病例的调查表进行了评估。在51名无基础疾病的患者中,复发的中位时间为9.5个月。复发发生在肺部的患者有18人,发生在其他部位的有33人。所有51名患者的5年生存率为70.6%,其中15名患者因复发而死亡,1名患者死于治疗相关并发症。肺部复发患者的5年生存率高于其他部位复发患者。初始化疗强度也会影响预后,化疗强度越低,5年生存率越高。在17名肺复发的幸存者中,最常见的治疗方法是化疗、手术和放疗相结合。常规化疗包括含铂方案和/或基于方案I的环磷酰胺和依托泊苷治疗。对于仅肺部复发或初始化疗强度较低的患者,挽救疗法显示出显著疗效,这凸显了对复发后治疗进行标准化前瞻性研究的必要性,并确定了长期幸存者出现晚期并发症的风险。
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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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