Personalized targeted glioblastoma therapies by <i>ex vivo</i> drug screening: Advanced brain tumor therapy clinical trial (ATTRACT).

TPS2097 Background: Targeted therapies used in a personalized treatment concept have revolutionized the management of several solid cancers. So far, various clinical trials aiming to introduce the concept of personalized targeted therapies in glioblastoma have failed, as no clinically meaningful responses were observed. Importantly, most clinical trials investigating molecular targeted therapies included all-comers and concentrated on genetic biomarkers to predict treatment response. Given the biological complexity of glioblastoma, genetic biomarkers might give only an insufficient insight into the response of a given patient, and more personalized approaches are warranted. As novel approaches to guide personalized treatment in glioblastoma are urgently needed, we designed a prospective clinical trial to investigate the novel approach of cultivated patient-derived tumor cells (PDCs) for ex vivo drug screening. Methods: In this randomized phase 2 study, we are testing the ability of PDC-based ex vivo drug screening to formulate a personalized recommendation for maintenance treatment in patients with newly diagnosed glioblastoma with unmethylated MGMT promoter after neurosurgical resection followed by combined radio-chemotherapy. Based on overall survival as the primary endpoint, we plan to include 240 patients (120 per group) to show with a power of 80% that we can increase the median survival from 12 to 17 months (hazard ratio 0.7). Patients are randomized 1:1 to either the standard group (no drug screening) or the intervention group (drug screening and personalized recommendation for maintenance treatment). In the intervention group, automated drug screening is performed on PDCs with 28 drugs used for treatment of solid tumors and hematological malignancies. Based on the cytotoxic/cytostatic activity of these drugs, as quantified by relative viability based on adenosine triphosphate levels, a molecular tumor board recommends a personalized treatment regimen. The first patient was enrolled in July 2024. Interim analysis of the ATTRACT study (NCT06512311) is expected in late 2027, and final results in 2030. Moreover, the clinical trial is accompanied by a comprehensive translational research program to gain insights into the biological underpinnings of treatment response in glioblastoma. Clinical trial information: NCT06512311 .

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Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.tps2097
Citations
2
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
3.25

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article

Personalized targeted glioblastoma therapies by ex vivo drug screening: Advanced brain tumor therapy clinical trial (ATTRACT).

Stefan Oberndorfer, Adelheid Wöehrer, Martha Nowosielski, Thomas Rudolf Pieber et al.
2 citations
Journal of Clinical Oncology
Glioma Diagnosis and Treatment
3.25
article

Personalized targeted glioblastoma therapies by ex vivo drug screening: Advanced brain tumor therapy clinical trial (ATTRACT).

Stefan Oberndorfer, Adelheid Wöehrer, Martha Nowosielski, Thomas Rudolf Pieber, Anna Sophie Berghoff, Julia Furtner, Franziska Eckert, Tadeja Urbanic Purkart, Annette Leibetseder, Franz König, Josef Pichler, Matthias Preusser, Sabine Spiegl‐Kreinecker, Georg Widhalm, Barbara Prietl, Amin El‐Heliebi, Maximilian J. Mair, Zoltán Spiró, Calvin Abdel Malak
article en
2 citations

Abstract

TPS2097 Background: Targeted therapies used in a personalized treatment concept have revolutionized the management of several solid cancers. So far, various clinical trials aiming to introduce the concept of personalized targeted therapies in glioblastoma have failed, as no clinically meaningful responses were observed. Importantly, most clinical trials investigating molecular targeted therapies included all-comers and concentrated on genetic biomarkers to predict treatment response. Given the biological complexity of glioblastoma, genetic biomarkers might give only an insufficient insight into the response of a given patient, and more personalized approaches are warranted. As novel approaches to guide personalized treatment in glioblastoma are urgently needed, we designed a prospective clinical trial to investigate the novel approach of cultivated patient-derived tumor cells (PDCs) for ex vivo drug screening. Methods: In this randomized phase 2 study, we are testing the ability of PDC-based ex vivo drug screening to formulate a personalized recommendation for maintenance treatment in patients with newly diagnosed glioblastoma with unmethylated MGMT promoter after neurosurgical resection followed by combined radio-chemotherapy. Based on overall survival as the primary endpoint, we plan to include 240 patients (120 per group) to show with a power of 80% that we can increase the median survival from 12 to 17 months (hazard ratio 0.7). Patients are randomized 1:1 to either the standard group (no drug screening) or the intervention group (drug screening and personalized recommendation for maintenance treatment). In the intervention group, automated drug screening is performed on PDCs with 28 drugs used for treatment of solid tumors and hematological malignancies. Based on the cytotoxic/cytostatic activity of these drugs, as quantified by relative viability based on adenosine triphosphate levels, a molecular tumor board recommends a personalized treatment regimen. The first patient was enrolled in July 2024. Interim analysis of the ATTRACT study (NCT06512311) is expected in late 2027, and final results in 2030. Moreover, the clinical trial is accompanied by a comprehensive translational research program to gain insights into the biological underpinnings of treatment response in glioblastoma. Clinical trial information: NCT06512311 .

Journal of Clinical OncologyVol. 43(16_suppl)
Danube Private University (AT), Innsbruck Medical University (AT), Universität Innsbruck (AT), Medical University of Graz (AT), Kepler Universitätsklinikum (AT), Center For Biomarker Research In Medicine (AT), Karl Landsteiner University of Health Sciences (AT), Medical University of Vienna (AT)
Ludwig Boltzmann Gesellschaft
Openalex Percentile: Top 9%
Glioma Diagnosis and Treatment
3.25
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