Sacred Heart Children's Hospital, Spokane, WA.
Nemours Children's Specialty Care and Wolfson Children's Hospital, Jacksonville, FL.
J Clin Oncol. 2022 Feb 10;40(5):459-467. doi: 10.1200/JCO.21.00803. Epub 2021 Dec 7.
Small cell undifferentiated (SCU) histology in hepatoblastoma (HB) tumors has historically been associated with a poor prognosis. Tumors from patients enrolled on Children's Oncology Group (COG) study AHEP0731 underwent institutional and central pathologic review for identification of SCU histology.
Patients with SCU histology identified at the local treating institution who had otherwise low-risk tumors were upstaged to the intermediate-risk treatment stratum, whereas those only identified by retrospective central review were treated per the local institution as low-risk. Patients with otherwise intermediate- or high-risk tumors remained in that treatment stratum, respectively. Central review was to be performed for all tissue samples obtained at any time point. Treatment was per local review, whereas analysis of outcome was based on central review.
Thirty-five patients had some elements (1%-25%) of SCU identified on central review of diagnostic specimens. All but two patient tissue sample retained nuclear INI1 expression. The presence of SCU histology did not correlate with age, alpha-fetoprotein level at diagnosis, or sex. The presence of SCU did not affect event-free survival (EFS). EFS at 5 years for patients with low-risk, intermediate-risk, and high-risk with SCU HB was 86% (95% CI, 33 to 98), 81% (95% CI, 57 to 92), and 29% (95% CI, 4 to 61), respectively, compared with EFS at 5 years for patients without SCU enrolled with low-risk, intermediate-risk, and high-risk of 87% (95% CI, 72 to 95), 88% (95% CI, 79 to 94), and 55% (95% CI, 32 to 74; = .17), respectively.
The presence of SCU histology in HB does not appear to adversely affect outcome. Future studies should be able to treat patients with SCU HB according to risk stratification without regard to the presence of SCU histology.
小细胞未分化(SCU)组织学在肝母细胞瘤(HB)肿瘤中历来与预后不良相关。在儿童肿瘤学组(COG)研究 AHEP0731 中,患者的肿瘤接受了机构和中心病理复查,以确定 SCU 组织学。
在当地治疗机构发现具有 SCU 组织学的患者,如果其他方面为低危肿瘤,则被升级为中危治疗分层,而仅通过回顾性中心复查发现的患者则按照当地机构的低危进行治疗。其他为中危或高危的患者分别留在该治疗分层。所有时间点获得的组织样本均应进行中心复查。治疗按照当地复查进行,而结果分析则基于中心复查。
35 名患者的诊断标本经中心复查有 1%-25%的 SCU 成分。除了两名患者外,所有患者的组织样本均保留核 INI1 表达。SCU 组织学的存在与年龄、诊断时甲胎蛋白水平或性别无关。SCU 的存在不影响无事件生存率(EFS)。具有 SCU 的低危、中危和高危 HB 患者的 5 年 EFS 分别为 86%(95%CI,33 至 98)、81%(95%CI,57 至 92)和 29%(95%CI,4 至 61),而无 SCU 的低危、中危和高危患者的 5 年 EFS 分别为 87%(95%CI,72 至 95)、88%(95%CI,79 至 94)和 55%(95%CI,32 至 74; =.17)。
HB 中 SCU 组织学的存在似乎不会对预后产生不利影响。未来的研究应该能够根据风险分层治疗 SCU HB 患者,而无需考虑 SCU 组织学的存在。