Long‐Term Outcomes of Patients With Relapsed/Refractory Neuroblastoma Treated on ANBL1221: A Report From the Children's Oncology Group

Results of COG ANBL1221 changed treatment paradigms for patients with relapsed/refractory neuroblastoma. Chemoimmunotherapy with irinotecan/temozolomide/dinutuximab is now used as both bridge therapy following suboptimal response to induction and as treatment in first relapse. Prospective data regarding long-term outcomes following this therapy have not been reported. Five-year progression-free survival (PFS) and overall survival (OS) for patients treated with chemoimmunotherapy were 22.6% ± 6.6% and 54.7% ± 7.7%, respectively. Patients with early disease progression following treatment on ANBL1221 tended to have been diagnosed with high-risk neuroblastoma at a younger age than those without early disease progression. A subset of chemoimmunotherapy-treated patients survived ≥2 years, but most all received additional therapy.

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Publication Details

Journal
Pediatric Blood & Cancer
Published
2026-07-23
DOI
https://doi.org/10.1002/1545-5017.70504
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Long‐Term Outcomes of Patients With Relapsed/Refractory Neuroblastoma Treated on ANBL1221: A Report From the Children's Oncology Group

Arlene Naranjo, Steven G. DuBois, Elizabeth Sokol, Rajen J. Mody et al.
Pediatric Blood & Cancer
Neuroblastoma Research and Treatments
article

Long‐Term Outcomes of Patients With Relapsed/Refractory Neuroblastoma Treated on ANBL1221: A Report From the Children's Oncology Group

Arlene Naranjo, Steven G. DuBois, Elizabeth Sokol, Rajen J. Mody, L Y Chen, Rochelle Bagatell, Navin Pinto
article en

Abstract

Results of COG ANBL1221 changed treatment paradigms for patients with relapsed/refractory neuroblastoma. Chemoimmunotherapy with irinotecan/temozolomide/dinutuximab is now used as both bridge therapy following suboptimal response to induction and as treatment in first relapse. Prospective data regarding long-term outcomes following this therapy have not been reported. Five-year progression-free survival (PFS) and overall survival (OS) for patients treated with chemoimmunotherapy were 22.6% ± 6.6% and 54.7% ± 7.7%, respectively. Patients with early disease progression following treatment on ANBL1221 tended to have been diagnosed with high-risk neuroblastoma at a younger age than those without early disease progression. A subset of chemoimmunotherapy-treated patients survived ≥2 years, but most all received additional therapy.

Pediatric Blood & Cancer
Children's Hospital of Philadelphia (US), Harvard University (US), University of Florida (US), Children's Hospital Colorado (US), Lurie Children's Hospital (US), Children's Oncology Group (US), C. S. Mott Children's Hospital (US), Dana-Farber/Boston Children's Cancer and Blood Disorders Center (US), Robert H. Lurie Comprehensive Cancer Center of Northwestern University, University of Colorado Denver (US)
United Therapeutics Corporation
Good health and well-being
Openalex Percentile: Top 9%
Neuroblastoma Research and Treatments
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Long‐Term Outcomes of Patients With Relapsed/Refractory Neuroblastoma Treated on ANBL1221: A Report From the Children's Oncology Group — Arlene Naranjo, Steven G. DuBois, et al. · Pediatric Blood & Cancer (2026) | TGRS Research Map | TGRS