Lerman Benjamin J, Li Yimei, Carlowicz Cecilia, Granger Meaghan, Cash Thomas, Sadanand Arhanti, Somers Katherine, Ranavaya Aeesha, Weiss Brian D, Choe Michelle, Foster Jennifer H, Pinto Navin, Morgenstern Daniel A, Rafael Margarida Simão, Streby Keri A, Zeno Rachel N, Mody Rajen, Yazdani Sahr, Desai Ami V, Macy Margaret E, Shusterman Suzanne, Federico Sara M, Bagatell Rochelle
Division of Oncology, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA.
Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA.
J Clin Oncol. 2023 Jan 20;41(3):508-516. doi: 10.1200/JCO.22.01273. Epub 2022 Oct 7.
Although chemoimmunotherapy is widely used for treatment of children with relapsed high-risk neuroblastoma (HRNB), little is known about timing, duration, and evolution of response after irinotecan/temozolomide/dinutuximab/granulocyte-macrophage colony-stimulating factor (I/T/DIN/GM-CSF) therapy.
Patients eligible for this retrospective study were age < 30 years at diagnosis of HRNB and received ≥ 1 cycle of I/T/DIN/GM-CSF for relapsed or progressive disease. Patients with primary refractory disease who progressed through induction were excluded. Responses were evaluated using the International Neuroblastoma Response Criteria.
One hundred forty-six patients were included. Tumors were -amplified in 50 of 134 (37%). Seventy-one patients (49%) had an objective response to I/T/DIN/GM-CSF (objective response; 29% complete response, 14% partial response [PR], 5% minor response [MR], 21% stable disease [SD], and 30% progressive disease). Of patients with SD or better at first post-I/T/DIN/GM-CSF disease evaluation, 22% had an improved response per International Neuroblastoma Response Criteria on subsequent evaluation (13% of patients with initial SD, 33% with MR, and 41% with PR). Patients received a median of 4.5 (range, 1-31) cycles. The median progression-free survival (PFS) was 13.1 months, and the 1-year PFS and 2-year PFS were 50% and 28%, respectively. The median duration of response was 15.9 months; the median PFS off all anticancer therapy was 10.4 months after discontinuation of I/T/DIN/GM-CSF.
Approximately half of patients receiving I/T/DIN/GM-CSF for relapsed HRNB had objective responses. Patients with initial SD were unlikely to have an objective response, but > 1 of 3 patients with MR/PR on first evaluation ultimately had complete response. I/T/DIN/GM-CSF was associated with extended PFS in responders both during and after discontinuation of treatment. This study establishes a new comparator for response and survival in patients with relapsed HRNB.
尽管化疗免疫疗法广泛用于复发性高危神经母细胞瘤(HRNB)患儿的治疗,但关于伊立替康/替莫唑胺/地努图希单抗/粒细胞巨噬细胞集落刺激因子(I/T/DIN/GM-CSF)治疗后的反应时机、持续时间及演变情况,人们了解甚少。
符合这项回顾性研究的患者为诊断HRNB时年龄<30岁,且因复发或疾病进展接受≥1周期I/T/DIN/GM-CSF治疗的患者。排除诱导治疗期间病情进展的原发性难治性疾病患者。使用国际神经母细胞瘤反应标准评估反应情况。
共纳入146例患者。134例患者中有50例(37%)肿瘤发生MYCN扩增。71例患者(49%)对I/T/DIN/GM-CSF有客观反应(客观反应;29%完全缓解,14%部分缓解[PR],5%轻微反应[MR],21%疾病稳定[SD],30%疾病进展)。在I/T/DIN/GM-CSF治疗后首次疾病评估时疾病稳定或更好的患者中,22%在后续评估中根据国际神经母细胞瘤反应标准反应有所改善(初始疾病稳定的患者中13%,轻微反应患者中33%,部分缓解患者中41%)。患者接受的周期数中位数为4.5(范围1 - 31)个周期。无进展生存期(PFS)中位数为13.1个月,1年PFS率和2年PFS率分别为50%和28%。反应持续时间中位数为15.9个月;停止I/T/DIN/GM-CSF治疗后,所有抗癌治疗停止后的PFS中位数为10.4个月。
接受I/T/DIN/GM-CSF治疗复发性HRNB的患者中约一半有客观反应。初始疾病稳定的患者不太可能有客观反应,但首次评估时轻微反应/部分缓解的患者中超过三分之一最终完全缓解。I/T/DIN/GM-CSF与治疗期间及停药后反应者的PFS延长相关。本研究为复发性HRNB患者的反应和生存建立了一个新的对照标准。