Abstract B020: Improved outcome for patients with alternative lengthening of telomeres (ALT) neuroblastoma randomized to tandem myeloablative therapy on COG ANBL0532

Abstract Background: Overall survival (OS) of high-risk neuroblastoma (HRNB) patients with alternative lengthening of telomeres (ALT) tumors (∼23% of patients) is low. Event-free survival (EFS) of HRNB patients in COG ANBL0532 was higher for tandem relative to single ASCT.We sought to determine if ALT HRNB patients on ANBL0532 benefited from tandem ASCT. Methods:We assessed telomere maintenance mechanisms (TMM), defined as per Cancer Res 80:2663, 2020, in 204 primary tumors from ANBL0532 patients as TERT+ (high TERT mRNA), ALT (positive for telomeric DNA C-circle assay) or ultrabright telomere foci (UTF), or no TMM. Due to non-proportional hazards, survival comparisons used the Improved Two-Stage Procedure (J Stat Comput Simul. 2017; 87:1877). Results: TMM status was: ALT n=48 (23.5%), TERT+ n=140 (68.6%), TMM negative n=16 (7.8%). Patients with TERT+ tumors more frequently progressed early, but 8-year OS was superior for TERT+ compared to ALT (58.1±4.6% vs 41.6±8.2%; p=0.0007), while 8-year OS for TMM negative was 67.7±12.2%. The 8-year OS for TERT+ patients randomized to single (n=67) vs tandem (n=59) ASCT was 56.9±6.7% vs 71.8±6.5% (p=0.32) and for ALT patients randomized to single (n=20) vs tandem (n=19) ASCT was 26.9±11.5% vs 61.1±13.5% (p=0.011).For patients on ANBL0532 who received dinutuximab post-consolidation therapy, the 8-year OS for TERT+ patients who underwent single (n=52) vs tandem (n=43) ASCT was 53.5±7.6% vs 75.8±7.8% (p=0.10) while for ALT patients who underwent single (n=13) vs tandem (n=10) ASCT it was 23.1±14.3% vs 77.8±16.4% (p=0.022). Conclusions:As previously reported, patients with ALT HRNB have inferior OS relative to TERT+ HRNB.TMM negative HRNB patients had apparently higher OS than ALT or TERT+ but small numbers preclude formal analyses. OS was significantly improved in ALT HRNB by tandem ASCT.These data support use of tandem myeloablative therapy for patients with ALT neuroblastoma until effective targeted therapies become available. Citation Format: Balakrishna Koneru, Trevor Burrow, Kristyn McCoy, Jonas Nance, Arlene Naranjo, Fan F. Zhang, Meredith S. Irwin, Julie R. Park, C. Patrick Reynolds. Improved outcome for patients with alternative lengthening of telomeres (ALT) neuroblastoma randomized to tandem myeloablative therapy on COG ANBL0532 [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pediatric Cancer Research; 2024 Sep 5-8; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl):Abstract nr B020.

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Journal
Cancer Research
Published
2024-09-05
DOI
https://doi.org/10.1158/1538-7445.pediatric24-b020
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1
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Neuroblastoma Research and Treatments
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article
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article

Abstract B020: Improved outcome for patients with alternative lengthening of telomeres (ALT) neuroblastoma randomized to tandem myeloablative therapy on COG ANBL0532

Arlene Naranjo, Jonas Nance, Julie R. Park, Balakrishna Koneru et al.
1 citations
Cancer Research
Neuroblastoma Research and Treatments
0.37
article

Abstract B020: Improved outcome for patients with alternative lengthening of telomeres (ALT) neuroblastoma randomized to tandem myeloablative therapy on COG ANBL0532

Arlene Naranjo, Jonas Nance, Julie R. Park, Balakrishna Koneru, Trevor A. Burrow, Meredith S. Irwin, Kristyn McCoy, C. Patrick Reynolds, Fan F. Zhang
article en
1 citations

Abstract

Abstract Background: Overall survival (OS) of high-risk neuroblastoma (HRNB) patients with alternative lengthening of telomeres (ALT) tumors (∼23% of patients) is low. Event-free survival (EFS) of HRNB patients in COG ANBL0532 was higher for tandem relative to single ASCT.We sought to determine if ALT HRNB patients on ANBL0532 benefited from tandem ASCT. Methods:We assessed telomere maintenance mechanisms (TMM), defined as per Cancer Res 80:2663, 2020, in 204 primary tumors from ANBL0532 patients as TERT+ (high TERT mRNA), ALT (positive for telomeric DNA C-circle assay) or ultrabright telomere foci (UTF), or no TMM. Due to non-proportional hazards, survival comparisons used the Improved Two-Stage Procedure (J Stat Comput Simul. 2017; 87:1877). Results: TMM status was: ALT n=48 (23.5%), TERT+ n=140 (68.6%), TMM negative n=16 (7.8%). Patients with TERT+ tumors more frequently progressed early, but 8-year OS was superior for TERT+ compared to ALT (58.1±4.6% vs 41.6±8.2%; p=0.0007), while 8-year OS for TMM negative was 67.7±12.2%. The 8-year OS for TERT+ patients randomized to single (n=67) vs tandem (n=59) ASCT was 56.9±6.7% vs 71.8±6.5% (p=0.32) and for ALT patients randomized to single (n=20) vs tandem (n=19) ASCT was 26.9±11.5% vs 61.1±13.5% (p=0.011).For patients on ANBL0532 who received dinutuximab post-consolidation therapy, the 8-year OS for TERT+ patients who underwent single (n=52) vs tandem (n=43) ASCT was 53.5±7.6% vs 75.8±7.8% (p=0.10) while for ALT patients who underwent single (n=13) vs tandem (n=10) ASCT it was 23.1±14.3% vs 77.8±16.4% (p=0.022). Conclusions:As previously reported, patients with ALT HRNB have inferior OS relative to TERT+ HRNB.TMM negative HRNB patients had apparently higher OS than ALT or TERT+ but small numbers preclude formal analyses. OS was significantly improved in ALT HRNB by tandem ASCT.These data support use of tandem myeloablative therapy for patients with ALT neuroblastoma until effective targeted therapies become available. Citation Format: Balakrishna Koneru, Trevor Burrow, Kristyn McCoy, Jonas Nance, Arlene Naranjo, Fan F. Zhang, Meredith S. Irwin, Julie R. Park, C. Patrick Reynolds. Improved outcome for patients with alternative lengthening of telomeres (ALT) neuroblastoma randomized to tandem myeloablative therapy on COG ANBL0532 [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pediatric Cancer Research; 2024 Sep 5-8; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl):Abstract nr B020.

Cancer ResearchVol. 84(17_Supplement)
Texas Tech University (US), St. Jude Children's Research Hospital (US), University of Toronto (CA), University of Florida (US), SickKids Foundation (CA), Texas Tech University Health Sciences Center (US), Florida College (US)
Good health and well-being
Openalex Percentile: Top 36%
Neuroblastoma Research and Treatments
0.37
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