Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Division of Biostatistics, University of Southern California and Children's Oncology Group, Monrovia, California, USA.
Cancer. 2024 Mar 1;130(5):792-802. doi: 10.1002/cncr.35084. Epub 2023 Oct 30.
The prognostic impact of positive lymph nodes (LN+) and/or singular loss of heterozygosity (LOH) of 1p or 16q were assessed in children with stage III favorable histology Wilms tumor (FHWT) enrolled on AREN0532 or AREN03B2 alone.
A total of 635 stage III FHWT vincristine/dactinomycin/doxorubicin (DD4A)-treated patients met inclusion criteria. Event-free survival (EFS) and overall survival are reported overall and by LN sampling, LN status, LOH 1p, LOH 16q, and a combination of LN status and singular LOH. Patients with unknown or positive combined LOH of 1p and 16q status and AREN03B2-only patients with unknown outcomes or treatment other than DD4A were excluded.
EFS did not differ by study, supporting pooling. Lack of LN sampling (hazard ratio [HR], 2.12; p = .0037), LN positivity (HR, 2.78; p = .0002), LOH 1p (HR, 2.18; p = .0067), and LOH 16q (HR, 1.72; p = .042) were associated with worse EFS. Compared with patients with both LN- and LOH-, those with negative nodes but positive LOH 1p or 16q and those with LN+ but LOH- for 1p or 16q had significantly worse EFS (HR, 3.05 and 3.57, respectively). Patients positive for both LN and LOH had the worst EFS (HR, 6.33; overall group factor, p < .0001).
Findings confirm LN+ status as an adverse prognostic factor amplified by presence of singular LOH 1p or 16q, supporting study of intensified therapy for patients with LN+ in combination with singular LOH in a prospective clinical trial.
本研究评估了单独接受 AREN0532 或 AREN03B2 方案治疗的 III 期低危组织学 Wilms 瘤(FHWT)患儿中,阳性淋巴结(LN+)和/或 1p 或 16q 杂合性缺失(LOH)的预后影响。
共有 635 例接受长春新碱/放线菌素 D/多柔比星(DD4A)治疗的 III 期 FHWT 患者符合纳入标准。本研究报告了总人群和根据 LN 取样、LN 状态、1p LOH、16q LOH 以及 LN 状态和单个 LOH 组合的无事件生存(EFS)和总生存。排除了无法评估或 AREN03B2 方案中 LN 状态和 1p 和 16q 同时 LOH 状态为阳性、或无法评估结局或除 DD4A 以外的其他治疗方案的患者。
本研究间 EFS 无差异,支持合并分析。缺乏 LN 取样(风险比 [HR],2.12;p=0.0037)、LN 阳性(HR,2.78;p=0.0002)、1p LOH(HR,2.18;p=0.0067)和 16q LOH(HR,1.72;p=0.042)与较差的 EFS 相关。与 LN-和 LOH-患者相比,LN 阴性但 1p 或 16q LOH 阳性的患者以及 LN+但 1p 或 16q LOH 阴性的患者 EFS 显著较差(HR 分别为 3.05 和 3.57)。同时 LN 和 LOH 阳性的患者 EFS 最差(HR,6.33;总体组因素,p<0.0001)。
研究结果证实 LN+状态是一个不良预后因素,与 1p 或 16q 单个 LOH 共同存在时更为显著,支持对 LN+患者进行前瞻性临床试验,研究强化治疗方案。