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日本威尔姆斯肿瘤研究-2 登记的肾肿瘤的结果:日本儿童癌症研究组(JCCG)的报告。

Outcome of renal tumors registered in Japan Wilms Tumor Study-2 (JWiTS-2): A report from the Japan Children's Cancer Group (JCCG).

机构信息

Department of Pediatric Surgery, Nihon University School of Medicine, Tokyo, Japan.

Division of Registration and Research for Childhood Cancer, National Center for Child Health and Development, Tokyo, Japan.

出版信息

Pediatr Blood Cancer. 2018 Jul;65(7):e27056. doi: 10.1002/pbc.27056. Epub 2018 Apr 6.

Abstract

BACKGROUND

Japan Wilms Tumor Study-2 (JWiTS-2) mandated central pathology review for all case registrations. The study aimed to compare the outcomes of patients with unilateral Wilms tumor enrolled on the JWiTS-1 and JWiTS-2 trials.

PROCEDURE

The JWiTS-2 trial (2006-2014), a prospective, single-arm study, required compulsory submission of histologic slides to central pathology, while in the JWiTS-1 trial, such submission was not compulsory. Relapse-free survival (RFS) and overall survival (OS) versus cases in the JWiTS-1 trial (1996-2005) were statistically evaluated.

RESULTS

Of 277 enrolled patients with primary renal tumors diagnosed by the central pathology review system, 225 patients with unilateral renal tumors were followed up over 9 years. The RFS and OS of Wilms tumor (n = 178) were 90.4% (P = 0.0003) and 96.8% (P = 0.054), respectively, as compared to 74.9% and 89.4% in JWiTS-1. RFS rates of stages I-III Wilms tumor in JWiTS-2 were more than 90%, although the outcome of stage IV Wilms tumor was significantly poorer (RFS: 66.2%) (P = 0.0094). RFS and OS of clear cell sarcoma of the kidney (CCSK; n = 31) were 82.4% (P = 0.30) and 91.3% (P = 0.42), respectively, as compared to 68.8% and 81.3% in JWiTS-1, and those of rhabdoid tumor of the kidney (RTK; n = 16) were 18.8% (P = 0.88) and 25.0% (P = 0.80), respectively, as compared to 23.5% and 23.5% in JWiTS-1.

CONCLUSIONS

RFS and OS for stages I-III Wilms tumor were improved in JWiTS-2 compared to JWiTS-1, whereas outcomes for stage IV Wilms tumor, CCSK, and RTK did not improve.

摘要

背景

日本威尔姆斯肿瘤研究-2 (JWiTS-2)要求对所有病例登记进行中心病理审查。该研究旨在比较单侧威尔姆斯肿瘤患者在 JWiTS-1 和 JWiTS-2 试验中的结果。

过程

JWiTS-2 试验(2006-2014)是一项前瞻性、单臂研究,要求强制性提交组织学切片进行中心病理学检查,而在 JWiTS-1 试验中,这种提交并非强制性的。通过统计学评估,无复发生存率(RFS)和总生存率(OS)与 JWiTS-1 试验(1996-2005)中的病例进行了比较。

结果

在通过中心病理审查系统诊断为原发性肾肿瘤的 277 名入组患者中,225 名单侧肾肿瘤患者接受了 9 年的随访。Wilms 肿瘤(n=178)的 RFS 和 OS 分别为 90.4%(P=0.0003)和 96.8%(P=0.054),而 JWiTS-1 中分别为 74.9%和 89.4%。JWiTS-2 中 I-III 期 Wilms 肿瘤的 RFS 率超过 90%,尽管 IV 期 Wilms 肿瘤的结果明显较差(RFS:66.2%)(P=0.0094)。JWiTS-2 中肾透明细胞肉瘤(CCSK;n=31)的 RFS 和 OS 分别为 82.4%(P=0.30)和 91.3%(P=0.42),而 JWiTS-1 中分别为 68.8%和 81.3%,JWiTS-2 中肾横纹肌肉瘤(RTK;n=16)的 RFS 和 OS 分别为 18.8%(P=0.88)和 25.0%(P=0.80),而 JWiTS-1 中分别为 23.5%和 23.5%。

结论

与 JWiTS-1 相比,JWiTS-2 中 I-III 期 Wilms 肿瘤的 RFS 和 OS 有所改善,而 IV 期 Wilms 肿瘤、CCSK 和 RTK 的结果并未改善。

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