Chemo-Immunotherapy Rescue for High-Risk Neuroblastoma Patients With Progressive Disease Before High-Dose Chemotherapy: Real-World Data From the SACHA-France Study

IF 2.3 3区 医学 Q2 HEMATOLOGY
Claudia Pasqualini, Stéphanie Proust, Gudrun Schleiermacher, Marion Gambart, Sarah Jannier, Arnaud Petit, Chrystelle Dupraz, Estelle Thebaud, Yves Reguerre, Lee Aymar Ndounga-Diakou, Salim Laghouat, Anne Sophie Defachelles, Pablo Berlanga
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引用次数: 0

Abstract

Background

Patients with high-risk neuroblastoma (HR-NBL) who experience disease progression (PD) during first-line treatment prior to high-dose chemotherapy (HDC) represent a rare and understudied subgroup, for whom treatment strategies are poorly defined and prognosis appears to be extremely poor.

Aims

We report real-world data on the off-label use of chemo-immunotherapy for HR-NBL patients with PD before HDC. The primary endpoint of our analysis is the best response during the chemo-immunotherapy treatment.

Methods

The SACHA-France registry prospectively documents safety and efficacy data on compassionate/off-label treatments for patients of ≤25 years old (NCT04477681).

Results

Between January 2020 and September 2024, 13 patients with HR-NBL received chemo-immunotherapy due to PD before HDC, and were included in SACHA-France. They had a median age of 3.4 years (1.3–8.0). Six patients had NMYC-amplified disease. Five PD occurred during/end-of-induction chemotherapy, and eight during temozolomide-based chemotherapy after initial insufficient metastatic response or toxicity. All but one had metastatic progression. The chemo-immunotherapy consisted of topotecan–cyclophosphamide (n = 9) or temozolomide–irinotecan (n = 4), combined with dinutuximab beta (dB) for a maximum of six cycles. Objective responses (ORs) were seen in five of 13 patients (38%)—four partial responses (PR) and one complete response (CR). Three out of the five patients with PD during/end of induction had PR, including two with NMYC-amplified tumors. Overall, six patients underwent tandem HDC, with two remaining progression-free after 1.7 and 2.1 years, and one remaining disease-free at 3.4 years.

Conclusion

Chemo-immunotherapy can benefit HR-NBL patients with PD before HDC, including those with progression during/at the end of the induction chemotherapy and NMYC amplification. These findings support its early inclusion in HR-NBL trials.

Abstract Image

在大剂量化疗前,化疗-免疫治疗对进展性高风险神经母细胞瘤患者的拯救:来自SACHA-France研究的真实世界数据
背景:高风险神经母细胞瘤(HR-NBL)患者在高剂量化疗(HDC)前的一线治疗期间经历疾病进展(PD)是一个罕见且研究不足的亚组,其治疗策略定义不清,预后似乎非常差。目的:我们报告了在HDC前使用化疗免疫疗法治疗HR-NBL患者PD的实际数据。我们分析的主要终点是化疗免疫治疗期间的最佳反应。方法:SACHA-France登记前瞻性地记录了≤25岁患者同情/标签外治疗的安全性和有效性数据(NCT04477681)。结果:2020年1月至2024年9月,13例HR-NBL患者在HDC前因PD接受了化疗免疫治疗,并纳入SACHA-France。他们的中位年龄为3.4岁(1.3-8.0岁)。6例患者患有nmyc扩增疾病。5例PD发生在/诱导结束化疗期间,8例发生在替莫唑胺基础化疗期间,最初的转移反应不足或毒性。除一人外,其余均有转移进展。化疗免疫治疗包括拓扑替康-环磷酰胺(n = 9)或替莫唑胺-伊立替康(n = 4),联合迪努妥昔单抗(dB),最多6个周期。13例患者中有5例(38%)出现客观缓解(ORs)——4例部分缓解(PR)和1例完全缓解(CR)。5名PD患者中有3名在诱导期间/结束时发生PR,包括2名nmyc扩增肿瘤患者。总体而言,6例患者接受了串联HDC,其中2例在1.7年和2.1年后无进展,1例在3.4年无疾病。结论:化疗免疫治疗可使HDC前的HR-NBL PD患者受益,包括诱导化疗期间/结束时进展和NMYC扩增的患者。这些发现支持将其早期纳入HR-NBL试验。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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