Dinutuximab beta versus naxitamab in the treatment of re-lapsed/refractory neuroblastoma in patients with stable disease, minor response or partial response and disease in bone or bone marrow: systematic review and matching-adjusted indirect comparison
Dinutuximab beta versus naxitamab in the treatment of re-lapsed/refractory neuroblastoma in patients with stable disease, minor response or partial response and disease in bone or bone marrow: systematic review and matching-adjusted indirect comparison
Objective: Dinutuximab beta (DB) and naxitamab (NAXI) with GM-CSF are used for maintenance treatment of relapsed/refractory neuroblastoma. The objective of this study was to systematically assess comparative efficacy of the two therapies within their designated indications in accordance with established clinical guidelines. Methods: Relevant evidence was identified in systematic literature review. Individual patient data (IPD) from prospective clinical trials of DB were assessed and data on patients with disease in bone or bone marrow, as assessed in MRI, CT, mIBG or biopsy, with incomplete response to previous therapy were included. Patients with complete response, progressive disease and/or soft tissue disease were excluded. DB population was adjusted for sex, MYCN amplification, disease type (relapsed, refractory), and disease site (bone marrow and/or bone) to balance aggregated characteristics of NAXI population. More characteristics were included in sensitivity analyses, including DB treatment without interleukin-2, as currently recommended. Overall response rate (ORR) was assessed as best response. Results: Aggregated data for NAXI from Study 201 (n = 52) and Study 230 (n = 38) and IPD from DB studies (APN311-202, APN311-304, c = 77) met the inclusion criteria. Compared to NAXI, DB significantly extended progression-free survival (PFS): hazard ratio, DB vs. NAXI of 0.47 (95% CI: 0.26 to 0.87, p = 0.015). ORR was 60.1% (95% CI: 48.5% to 71.6%) for DB vs. 43.3% (33.1% to 53.6%) for NAXI (ORR odds ratio, DB vs. NAXI was 1.97, 95% CI: 1.02 to 3.80, p = 0.044). Sensitivity analyses and unadjusted comparisons supported the results. Conclusion: In the indirect comparison, dinutuximab beta significantly extended PFS and increased ORR compared to naxitamab.
dinutuximab beta, matching-adjusted indirect comparison, naxitamab, relapsed/refractory neuroblastoma, systematic review
Lode, Holger N.
c6482d76-8235-40b9-adbd-1d3cae4ac2c3
Holko, Przemysław
fc205ead-5907-4945-bfe9-a4de8b578a39
Wieczorek, Aleksandra
5890e74a-d232-458e-889e-3fc4ebae6b04
Gray, Juliet
12d5e17c-97bb-4d6d-8fc4-3914b730ed42
22 August 2025
Lode, Holger N.
c6482d76-8235-40b9-adbd-1d3cae4ac2c3
Holko, Przemysław
fc205ead-5907-4945-bfe9-a4de8b578a39
Wieczorek, Aleksandra
5890e74a-d232-458e-889e-3fc4ebae6b04
Gray, Juliet
12d5e17c-97bb-4d6d-8fc4-3914b730ed42
Lode, Holger N., Holko, Przemysław and Wieczorek, Aleksandra
,
et al.
(2025)
Dinutuximab beta versus naxitamab in the treatment of re-lapsed/refractory neuroblastoma in patients with stable disease, minor response or partial response and disease in bone or bone marrow: systematic review and matching-adjusted indirect comparison.
Cancers, 17 (17), [2723].
(doi:10.3390/cancers17172723).
Abstract
Objective: Dinutuximab beta (DB) and naxitamab (NAXI) with GM-CSF are used for maintenance treatment of relapsed/refractory neuroblastoma. The objective of this study was to systematically assess comparative efficacy of the two therapies within their designated indications in accordance with established clinical guidelines. Methods: Relevant evidence was identified in systematic literature review. Individual patient data (IPD) from prospective clinical trials of DB were assessed and data on patients with disease in bone or bone marrow, as assessed in MRI, CT, mIBG or biopsy, with incomplete response to previous therapy were included. Patients with complete response, progressive disease and/or soft tissue disease were excluded. DB population was adjusted for sex, MYCN amplification, disease type (relapsed, refractory), and disease site (bone marrow and/or bone) to balance aggregated characteristics of NAXI population. More characteristics were included in sensitivity analyses, including DB treatment without interleukin-2, as currently recommended. Overall response rate (ORR) was assessed as best response. Results: Aggregated data for NAXI from Study 201 (n = 52) and Study 230 (n = 38) and IPD from DB studies (APN311-202, APN311-304, c = 77) met the inclusion criteria. Compared to NAXI, DB significantly extended progression-free survival (PFS): hazard ratio, DB vs. NAXI of 0.47 (95% CI: 0.26 to 0.87, p = 0.015). ORR was 60.1% (95% CI: 48.5% to 71.6%) for DB vs. 43.3% (33.1% to 53.6%) for NAXI (ORR odds ratio, DB vs. NAXI was 1.97, 95% CI: 1.02 to 3.80, p = 0.044). Sensitivity analyses and unadjusted comparisons supported the results. Conclusion: In the indirect comparison, dinutuximab beta significantly extended PFS and increased ORR compared to naxitamab.
Text
cancers-3808240
- Accepted Manuscript
Text
cancers-17-02723-v2
- Version of Record
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Accepted/In Press date: 15 August 2025
Published date: 22 August 2025
Keywords:
dinutuximab beta, matching-adjusted indirect comparison, naxitamab, relapsed/refractory neuroblastoma, systematic review
Identifiers
Local EPrints ID: 505283
URI: http://eprints.soton.ac.uk/id/eprint/505283
ISSN: 2072-6694
PURE UUID: 5e16388e-c31c-4a58-922c-a990a6892be2
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Date deposited: 06 Oct 2025 16:41
Last modified: 26 Nov 2025 02:38
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Author:
Holger N. Lode
Author:
Przemysław Holko
Author:
Aleksandra Wieczorek
Corporate Author: et al.
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