Abstract A043: Genomically-tailored multi-agent precision medicine clinical trial for adults with recurrent glioblastoma

Abstract Background: Existing salvage therapies for recurrent glioblastoma (rGBM) have limited efficacy, with median survival of approximately 9 months. Given the complex molecular heterogeneity of GBM, single-target approaches have consistently failed as a treatment strategy. We conducted a phase 1 clinical trial to assess the feasibility, safety, and efficacy of a genomically-tailored multi-agent regimen in 30 adults with surgically-treated rGBM. Methods: Adults with IDH-wildtype glioblastoma (n=29) or grade 4 IDH-mutant astrocytoma (n=1) were consented and underwent clinically indicated surgery for recurrent disease. Comprehensive genomic profiling was performed on the recurrent tumors, and results for each patient were discussed at an individualized molecular tumor board to determine a personalized treatment regimen combining up to 4 FDA-approved drugs, including one cytotoxic agent as backbone. Results: A total of 12 drugs were used in 18 combinations – the most common regimen was lomustine, afatinib, and abemaciclib (n=8). The most common toxicities included cytopenias, rash, and gastrointestinal symptoms, requiring frequent dose reductions. Measured from surgery at trial enrollment, progression-free survival at 6 months (PFS-6) was 40%, overall survival at 9 months (OS-9) was 73%, and median OS was 12.7 months. After trial therapy, genomic profiling performed on subsequent recurrent tumor specimens identified genetic evolution corresponding to putative treatment resistance mechanisms. Conclusions: Implementation of individualized treatment regimens in a timely fashion was feasible for patients with surgically resectable rGBM. Overall efficacy compared to a contemporary patient cohort not treated with experimental regimens was modest, with full dosing of most combination therapies limited by toxicities. Citation Format: David A. Solomon, Elise Chen, Nancy Ann Oberheim Bush, Jennifer Grabowsky, Cassie Kline, Deanna Kroetz, Jennie Taylor, Javier Villanueva-Meyer, Annette Molinaro, John de Groot, Nicholas Butowski, Meghan Tedesco, Jane Rabbitt, Joanna Phillips, Shawn Hervey-Jumper, Manish Aghi, Mitchel Berger, Edward Chang, Susan Chang, Jennifer Clarke. Genomically-tailored multi-agent precision medicine clinical trial for adults with recurrent glioblastoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Brain Cancer; 2026 Mar 23-25; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(6_Suppl):Abstract nr A043.

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Journal
Cancer Research
Published
2026-03-23
DOI
https://doi.org/10.1158/1538-7445.brain26-a043
Primary Topic
Glioma Diagnosis and Treatment
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article
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article

Abstract A043: Genomically-tailored multi-agent precision medicine clinical trial for adults with recurrent glioblastoma

Jennifer A. Grabowsky, Meghan Tedesco, Jane Rabbitt, Edward S. Chang et al.
Cancer Research
Glioma Diagnosis and Treatment
article

Abstract A043: Genomically-tailored multi-agent precision medicine clinical trial for adults with recurrent glioblastoma

Jennifer A. Grabowsky, Meghan Tedesco, Jane Rabbitt, Edward S. Chang, M. K. Aghi, Joanna J. Phillips, Jennifer Clarke, Cassie Kline, J. S. De Groot, Jennie Taylor, David A. Solomon, Nicholas Butowski, Nancy Ann Oberheim Bush, Shi Chang, Annette Molinaro, Javier Villanueva-Meyer, Deanna Kroetz, Mitchel Berger, Elise Chen, Shawn Hervey-Jumper
article en

Abstract

Abstract Background: Existing salvage therapies for recurrent glioblastoma (rGBM) have limited efficacy, with median survival of approximately 9 months. Given the complex molecular heterogeneity of GBM, single-target approaches have consistently failed as a treatment strategy. We conducted a phase 1 clinical trial to assess the feasibility, safety, and efficacy of a genomically-tailored multi-agent regimen in 30 adults with surgically-treated rGBM. Methods: Adults with IDH-wildtype glioblastoma (n=29) or grade 4 IDH-mutant astrocytoma (n=1) were consented and underwent clinically indicated surgery for recurrent disease. Comprehensive genomic profiling was performed on the recurrent tumors, and results for each patient were discussed at an individualized molecular tumor board to determine a personalized treatment regimen combining up to 4 FDA-approved drugs, including one cytotoxic agent as backbone. Results: A total of 12 drugs were used in 18 combinations – the most common regimen was lomustine, afatinib, and abemaciclib (n=8). The most common toxicities included cytopenias, rash, and gastrointestinal symptoms, requiring frequent dose reductions. Measured from surgery at trial enrollment, progression-free survival at 6 months (PFS-6) was 40%, overall survival at 9 months (OS-9) was 73%, and median OS was 12.7 months. After trial therapy, genomic profiling performed on subsequent recurrent tumor specimens identified genetic evolution corresponding to putative treatment resistance mechanisms. Conclusions: Implementation of individualized treatment regimens in a timely fashion was feasible for patients with surgically resectable rGBM. Overall efficacy compared to a contemporary patient cohort not treated with experimental regimens was modest, with full dosing of most combination therapies limited by toxicities. Citation Format: David A. Solomon, Elise Chen, Nancy Ann Oberheim Bush, Jennifer Grabowsky, Cassie Kline, Deanna Kroetz, Jennie Taylor, Javier Villanueva-Meyer, Annette Molinaro, John de Groot, Nicholas Butowski, Meghan Tedesco, Jane Rabbitt, Joanna Phillips, Shawn Hervey-Jumper, Manish Aghi, Mitchel Berger, Edward Chang, Susan Chang, Jennifer Clarke. Genomically-tailored multi-agent precision medicine clinical trial for adults with recurrent glioblastoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Brain Cancer; 2026 Mar 23-25; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(6_Suppl):Abstract nr A043.

Cancer ResearchVol. 86(6_Supplement)
Children's Hospital of Philadelphia (US), University of California, San Francisco (US), Ohio University (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 13%
Glioma Diagnosis and Treatment
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