CTP-03. A Phase 2 study of alisertib in combination therapy for newly diagnosed Atypical Teratoid/Rhabdoid Tumor (AT/RT)- Results from SJATRT strata B and C

Abstract BACKGROUND Atypical teratoid/rhabdoid (AT/RT) is an aggressive pediatric brain tumor, prevalent in children < 3 years(Y) of age. Though treatment with surgery, radiation and chemotherapy has improved clinical outcome, the cure rate remains suboptimal. Molecularly, AT/RT demonstrates alterations in SMARCB1 and SMARCA4 and methylation profiles sub-classify AT/RTs into AT/RT-MYC(MYC), AT/RT-SHH(SHH) and AT/RT-TYR(TYR). METHODS We conducted a phase 2 study of Aurora Kinase A inhibitor, alisertib, in combination with chemotherapy and radiotherapy (RT) in newly diagnosed AT/RT (Stratum B [B1-M0 & B2-M+]: < 36 months; Stratum C [C1-M0 & C2-M+] - ≥ 36 months). Stratum B1 patients received focal RT at ≥12 months of age and patients on stratum C1 (23.4 Gy) and C2 (36 Gy) received post-operative CSI. RESULTS 71 evaluable patients were enrolled on strata B1 (n=30), B2 (n=17), C1(n=13) and C2 (n=11). For, B1 (SHH:18, TYR:7, MYC:3, NC:2) the 3Y PFS and OS were 30.0% and 56.7%. B2 (SHH:8, TYR:7, MYC:2) had a 3Y PFS and OS of 0 and 17.6% and was closed early at PI discretion due to lack of efficacy. Stratum C1 (SHH:4, TYR:2 & MYC:6, NA:1, NC:1) the 3Y PFS and OS were 84.6% & 100.0% and for C2 (SHH:6 and MYC:3, NC:2), 63.6% was the 3Y PFS and OS. SHH patients had better PFS (p=0.036) in C2 in comparison to MYC. Strata C1 and C2 did not reach target accrual. There were no unexpected toxicities, most common grade 3 toxicities were related to myelosuppression. CONCLUSION Combination of alisertib with chemotherapy and RT was well tolerated, however, it didn’t improve survival in newly diagnosed AT/RT. The study confirms, albeit in small numbers, prior results of a higher survival for M0 patients with post-operative CSI in ≥ 36-month-old (C1). The PFS in M+ ≥ 36-month-old patients (C2) was higher with CSI than previously reported. Molecular subclass was not associated with outcome except in SHH in C2.

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Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.0575
Primary Topic
Chromatin Remodeling and Cancer
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article
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article

CTP-03. A Phase 2 study of alisertib in combination therapy for newly diagnosed Atypical Teratoid/Rhabdoid Tumor (AT/RT)- Results from SJATRT strata B and C

Anne Bendel, Eroica Soans, Thomas E. Merchant, Quynh T. Tran et al.
Neuro-Oncology
Chromatin Remodeling and Cancer
article

CTP-03. A Phase 2 study of alisertib in combination therapy for newly diagnosed Atypical Teratoid/Rhabdoid Tumor (AT/RT)- Results from SJATRT strata B and C

Anne Bendel, Eroica Soans, Thomas E. Merchant, Quynh T. Tran, Alex Breuer, Arzu Onar Thomas, Brent A. Orr, Emily Hanzlik, Michelle N. Richardson, Amar Gajjar, John R. Crawford, Lindsay Kilburn, Catherine A. Billups, Congyu Lu, Giles W Robinson, Sonia Partap, Sandeep Kumar Dhanda, Anjali Singh, Wenjie Qi, Santhosh A. Upadhyaya, Xin Zhou, Patricia Baxter, Aditi Bagchi, Paul Klimo, Dolly Aguillera
article en

Abstract

Abstract BACKGROUND Atypical teratoid/rhabdoid (AT/RT) is an aggressive pediatric brain tumor, prevalent in children < 3 years(Y) of age. Though treatment with surgery, radiation and chemotherapy has improved clinical outcome, the cure rate remains suboptimal. Molecularly, AT/RT demonstrates alterations in SMARCB1 and SMARCA4 and methylation profiles sub-classify AT/RTs into AT/RT-MYC(MYC), AT/RT-SHH(SHH) and AT/RT-TYR(TYR). METHODS We conducted a phase 2 study of Aurora Kinase A inhibitor, alisertib, in combination with chemotherapy and radiotherapy (RT) in newly diagnosed AT/RT (Stratum B [B1-M0 & B2-M+]: < 36 months; Stratum C [C1-M0 & C2-M+] - ≥ 36 months). Stratum B1 patients received focal RT at ≥12 months of age and patients on stratum C1 (23.4 Gy) and C2 (36 Gy) received post-operative CSI. RESULTS 71 evaluable patients were enrolled on strata B1 (n=30), B2 (n=17), C1(n=13) and C2 (n=11). For, B1 (SHH:18, TYR:7, MYC:3, NC:2) the 3Y PFS and OS were 30.0% and 56.7%. B2 (SHH:8, TYR:7, MYC:2) had a 3Y PFS and OS of 0 and 17.6% and was closed early at PI discretion due to lack of efficacy. Stratum C1 (SHH:4, TYR:2 & MYC:6, NA:1, NC:1) the 3Y PFS and OS were 84.6% & 100.0% and for C2 (SHH:6 and MYC:3, NC:2), 63.6% was the 3Y PFS and OS. SHH patients had better PFS (p=0.036) in C2 in comparison to MYC. Strata C1 and C2 did not reach target accrual. There were no unexpected toxicities, most common grade 3 toxicities were related to myelosuppression. CONCLUSION Combination of alisertib with chemotherapy and RT was well tolerated, however, it didn’t improve survival in newly diagnosed AT/RT. The study confirms, albeit in small numbers, prior results of a higher survival for M0 patients with post-operative CSI in ≥ 36-month-old (C1). The PFS in M+ ≥ 36-month-old patients (C2) was higher with CSI than previously reported. Molecular subclass was not associated with outcome except in SHH in C2.

Neuro-OncologyVol. 27(Supplement_5)
Children's Hospital of Orange County (US), St. Jude Children's Research Hospital (US), Children's National (US), Baylor College of Medicine (US), Children's Minnesota (US), Children's Healthcare of Atlanta (US), Texas Children's Hospital (US), Children's Cancer Center (US), C. S. Mott Children's Hospital (US), Le Bonheur Children's Hospital (US), Stanford University (US)
Openalex Percentile: Top 70%
Chromatin Remodeling and Cancer
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