AUTHOR=Ozkaynak M. Fevzi , Gilman Andrew L. , London Wendy B. , Naranjo Arlene , Diccianni Mitchell B. , Tenney Sheena C. , Smith Malcolm , Messer Karen S. , Seeger Robert , Reynolds C. Patrick , Smith L. Mary , Shulkin Barry L. , Parisi Marguerite , Maris John M. , Park Julie R. , Sondel Paul M. , Yu Alice L. 

TITLE=A Comprehensive Safety Trial of Chimeric Antibody 14.18 With GM-CSF, IL-2, and Isotretinoin in High-Risk Neuroblastoma Patients Following Myeloablative Therapy: Children’s Oncology Group Study ANBL0931

JOURNAL=Frontiers in Immunology

VOLUME=Volume 9 - 2018

YEAR=2018

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2018.01355

DOI=10.3389/fimmu.2018.01355

ISSN=1664-3224

ABSTRACT=Purpose: A Phase 3 randomized study (COG ANBL0032) demonstrated significantly improved outcome by adding immunotherapy with ch14.18 antibody to isotretinoin as post-consolidation therapy for high-risk neuroblastoma (NB). This study, ANBL0931, was designed to collect FDA-required safety/toxicity data to support FDA registration of ch14.18. 

Experimental Design: Newly diagnosed high-risk NB patients who achieved at least a partial response to induction therapy and received myeloablative consolidation with stem cell rescue  were enrolled to receive 6 courses of isotretinoin with five concomitant cycles of ch14.18 combined with GM-CSF or IL2. Ch14.18 infusion time was 10-20 hours per dose. Blood was collected for cytokine analysis and its association with toxicities and outcome.

Results: Of 105 patients enrolled, five patients developed protocol-defined unacceptable toxicities. The most common Grade ≥3 non-hematologic toxicities of immunotherapy for cycles 1-5, respectively, were neuropathic pain (41%, 28%, 22%, 31%, 24%), hypotension (10%, 17%, 4%, 14%, 8%), allergic reactions (3%, 10%, 5%, 7%, 2%), capillary leak syndrome (1%, 4%, 0%, 2%, 0%), and fever (21%, 59%, 6%, 32%, 5%). The 3-year event-free survival and overall survival were 67.6±4.8% and 79.1±4.2%, respectively. Allergic reaction during course 1 was associated with elevated serum levels of IL-1Ra and IFN, while severe hypotension during this course was associated with low IL5 and nitrate. Higher pretreatment CXCL9 level was associated with poorer EFS.

Conclusions: This study has confirmed the significant, but manageable treatment-related toxicities of this immunotherapy and identified possible cytokine biomarkers associated with select toxicities and outcome.  EFS and OS appear similar to that previously reported on ANBL0032.