1 Roswell Park Cancer Institute, Buffalo, NY.
2 University of Florida, Gainesville, FL.
J Clin Oncol. 2019 Jan 10;37(2):115-124. doi: 10.1200/JCO.18.00419. Epub 2018 Nov 16.
Infants with stage 4S neuroblastoma usually have favorable outcomes with observation or minimal chemotherapy. However, young infants with symptoms secondary to massive hepatomegaly or with unfavorable tumor biology are at high risk of death. Our aim was to improve outcomes for patients with symptomatic and/or unfavorable biology 4S neuroblastoma with a uniform treatment approach using a biology- and response-based algorithm.
The subset of patients with 4S disease with MYCN-not amplified tumors with impaired or impending organ dysfunction, or with unfavorable histology and/or diploid DNA index, were eligible. Patients were assigned to receive two, four, or eight cycles of chemotherapy on the basis of histology, diploid DNA index, chromosome arm 1p or 11q loss of heterozygosity (LOH) status, and symptoms.
Forty-nine eligible patients were enrolled: 41 were symptomatic and 28 had unfavorable biology. Seventeen patients (symptomatic, favorable biology) were assigned two cycles, 21 patients (any unfavorable biologic feature without 1p or 11q LOH) were assigned four cycles, and 11 patients (unfavorable biology including 1p and/or 11q LOH [n = 7] or symptomatic with unknown biology [n = 4]), were assigned eight cycles. The 3-year overall survival was 81.4% ± 5.8%. Eight of nine deaths were in patients younger than 2 months of age at diagnosis (median, 9 days [range, 1 to 68 days]): five acute deaths were a result of hepatomegaly and associated toxicities; two were a result of late relapse in patients with unfavorable biology; and two were a result of treatment complications. No deaths occurred after protocol-mandated pre-emptive treatment of infants younger than 2 months with hepatomegaly, regardless of symptoms. A new scoring algorithm for emergent chemotherapy in patients with 4S disease was developed on the basis of this experience.
The outcome for 4S neuroblastoma can be improved with pre-emptive chemotherapy for evolving hepatomegaly or other baseline comorbidities in infants younger than 2 months of age.
患有 4S 期神经母细胞瘤的婴儿通常通过观察或接受最小剂量的化疗即可获得良好的预后。然而,因巨大肝肿大而出现症状或具有不良肿瘤生物学特征的小婴儿,死亡风险较高。我们的目的是通过使用基于生物学和反应的算法,为具有症状和/或不良生物学特征的 4S 神经母细胞瘤患者提供一种统一的治疗方法,从而改善患者的预后。
符合条件的患者为患有 4S 疾病且 MYCN 未扩增、伴有进行性器官功能障碍或具有不良组织学和/或二倍体 DNA 指数的婴儿。根据组织学、二倍体 DNA 指数、染色体 1p 或 11q 杂合性丢失(LOH)状态和症状,将患者分配接受 2、4 或 8 个周期的化疗。
共纳入 49 例符合条件的患者:41 例有症状,28 例有不良生物学特征。17 例(有症状,生物学特征良好)患者接受 2 个周期治疗,21 例(无 1p 或 11q LOH 的任何不良生物学特征)患者接受 4 个周期治疗,11 例(包括 1p 和/或 11q LOH 的不良生物学特征[7 例]或有症状但生物学特征未知[4 例])患者接受 8 个周期治疗。3 年总生存率为 81.4%±5.8%。9 例死亡病例中,有 8 例患者的诊断年龄小于 2 个月(中位年龄 9 天[范围 1 至 68 天]):5 例急性死亡是由于肝肿大和相关毒性所致;2 例是由于具有不良生物学特征的患者发生晚期复发所致;2 例是由于治疗并发症所致。在 protocol-mandated 方案中,对于小于 2 个月的肝肿大婴儿,无论有无症状,都进行了预防性治疗,此后未发生死亡。根据这一经验,为 4S 疾病制定了一种新的紧急化疗评分算法。
对于小于 2 个月的婴儿,对于进展性肝肿大或其他基线合并症,可以进行预防性化疗,从而改善 4S 神经母细胞瘤的预后。