A clinical observational study of dinutuximab beta as first-line maintenance treatment for patients with high-risk neuroblastoma in China

被引:0
作者
Yu, Xuedi [1 ]
Kang, Suyi [1 ]
Ge, Junjie [1 ]
Wang, Jingfu [1 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Shandong Canc Hosp & Inst, Dept Pediat Oncol, Jinan 250000, Peoples R China
关键词
High-risk neuroblastoma; Dinutuximab beta; GD2-antibody immunotherapy; GM-CSF; First-line maintenance; Chemotherapy; ANTI-GD2; ANTIBODY; GANGLIOSIDE GD2; INTERLEUKIN-2; EXPRESSION;
D O I
10.1186/s12887-025-05568-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundHigh-risk neuroblastoma (HR-NB) is associated with high metastatic and relapse rates that require intensive multimodal treatment. We evaluated the efficacy and safety of dinutuximab beta as first-line maintenance immunotherapy in pediatric patients with HR-NB in real-world clinical settings in China.MethodsWe retrospectively reviewed the clinical records of pediatric patients with newly diagnosed HR-NB in the hospital from October 2021 to November 2023. Patients treated with dinutuximab beta in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF) and isotretinoin as the first-line maintenance therapy were included in this study. Among patients with residual disease after completing induction and consolidation treatment, those with partial response (PR) or very good partial response (VGPR) except for bone marrow (BM) residue were also administrated vincristine/irinotecan/temozolomide (VIT) chemotherapy.ResultsFifty-one patients with newly diagnosed HR-NB who achieved at least PR before immunotherapy were evaluated. At the end of immunotherapy, the objective response rate (ORR) in 33 patients with evidence of disease was 60.6% (95% confidence interval (CI), 42.1-77.1%) and the complete response rate (CRR; n = 18) was 54.5% (95% CI, 36.4-71.9%). The 2-year event-free survival (EFS) rate and overall survival (OS) rate were 80.1% (95% CI, 66.2-88.8%) and 97.6% (95% CI, 84.3-99.7%), respectively. The 2-year EFS rate was higher in patients with CR (94.4%; 95% CI, 66.6-99.2%) than in non-CR patients (72.6%; 95% CI, 53.9-84.7%). Dinutuximab beta was well tolerated in patients and had fewer side effects, which decreased over time. Co-treatment of dinutuximab beta with VIT chemotherapy did not require discontinuation in patients undergoing immunochemotherapy.ConclusionThe study showed promising efficacy and safety of dinutuximab beta as the first-line maintenance immunotherapy for pediatric patients with HR-NB. Notably, the combination of dinutuximab beta with GM-CSF and VIT chemotherapy could be used for treating patients who did not achieve CR after previous multimodal therapy.
引用
收藏
页数:11
相关论文
共 40 条
[1]  
[Anonymous], Qarziba (previously Dinutuximab beta EUSA and Dinutuximab beta Apeiron)
[2]  
[Anonymous], On. August 16, 2021, the information on the pending collection of drug approval documents was released
[3]  
BARKER E, 1991, CANCER RES, V51, P144
[4]   REVISIONS OF THE INTERNATIONAL CRITERIA FOR NEUROBLASTOMA DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT [J].
BRODEUR, GM ;
PRITCHARD, J ;
BERTHOLD, F ;
CARLSEN, NLT ;
CASTEL, V ;
CASTLEBERRY, RP ;
DEBERNARDI, B ;
EVANS, AE ;
FAVROT, M ;
HEDBORG, F ;
KANEKO, M ;
KEMSHEAD, J ;
LAMPERT, F ;
LEE, REJ ;
LOOK, AT ;
PEARSON, ADJ ;
PHILIP, T ;
ROALD, B ;
SAWADA, T ;
SEEGER, RC ;
TSUCHIDA, Y ;
VOUTE, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (08) :1466-1477
[5]  
Cancer Statistics SEER, Review. 1975-2009-Previous Version-SEER Cancer Statistics Review
[6]   GANGLIOSIDE GD2 SPECIFIC MONOCLONAL ANTIBODY-3F8 - A PHASE-I STUDY IN PATIENTS WITH NEUROBLASTOMA AND MALIGNANT-MELANOMA [J].
CHEUNG, NKV ;
LAZARUS, H ;
MIRALDI, FD ;
ABRAMOWSKY, CR ;
KALLICK, S ;
SAARINEN, UM ;
SPITZER, T ;
STRANDJORD, SE ;
COCCIA, PF ;
BERGER, NA .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (09) :1430-1440
[7]  
Collaborative Group on GD2 Monoclonal Antibody in the Treatment of Neuroblastoma, 2022, J Clin Pediatr, V40, P14
[8]   Childhood cancer survival in Europe 1999-2007: results of EUROCARE-5-a population-based study [J].
Gatta, Gemma ;
Botta, Laura ;
Rossi, Silvia ;
Aareleid, Tiiu ;
Bielska-Lasota, Magdalena ;
Clavel, Jacqueline ;
Dimitrova, Nadya ;
Jakab, Zsuzsanna ;
Kaatsch, Peter ;
Lacour, Brigitte ;
Mallone, Sandra ;
Marcos-Gragera, Rafael ;
Minicozzi, Pamela ;
Sanchez-Perez, Maria-Jose ;
Sant, Milena ;
Santaquilani, Mariano ;
Stiller, Charles ;
Tavilla, Andrea ;
Trama, Annalisa ;
Visser, Otto ;
Peris-Bonet, Rafael .
LANCET ONCOLOGY, 2014, 15 (01) :35-47
[9]   HIGH-LEVEL EXPRESSION OF CHIMERIC ANTIBODIES USING ADAPTED CDNA VARIABLE REGION CASSETTES [J].
GILLIES, SD ;
LO, KM ;
WESOLOWSKI, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 125 (1-2) :191-202
[10]  
Gray J, 2022, J CLIN ONCOL, V40