TY - JOUR
T1 - Personalized targeted glioblastoma therapies by ex vivo drug screening
T2 - Study protocol of the Advanced brain Tumor TheRApy Clinical Trial (ATTRACT)
AU - ATTRACT study group
AU - Berghoff, Anna Sophie
AU - Mair, Maximilian J
AU - Spiró, Zoltán
AU - Abdel Malak, Calvin
AU - El-Heliebi, Amin
AU - Eckert, Franziska
AU - Furtner, Julia
AU - König, Franz
AU - Leibetseder, Annette
AU - Nowosielski, Martha
AU - Oberndorfer, Stefan
AU - Prietl, Barbara
AU - Pichler, Josef
AU - Pieber, Thomas R
AU - Spiegl-Kreinecker, Sabine
AU - Urbanic Purkart, Tadeja
AU - Wöhrer, Adelheid
AU - Widhalm, Georg
AU - Preusser, Matthias
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.
PY - 2025
Y1 - 2025
N2 - BACKGROUND: Novel approaches to guide personalized treatment in glioblastoma are urgently needed. Given the poor predictive value of genetic biomarkers in glioblastoma, we are conducting 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 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 will be 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 will be performed on PDCs with 28 drugs used for the treatment of solid tumors and hematological malignancies. Based on the cytotoxic activity of these drugs, as quantified by relative viability based on adenosine triphosphate levels, a molecular tumor board will recommend a personalized treatment regimen.RESULTS: 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.TRIAL REGISTRATION: The ATTRACT trial is registered under the ID NCT06512311 (https://clinicaltrials.gov/study/NCT06512311).
AB - BACKGROUND: Novel approaches to guide personalized treatment in glioblastoma are urgently needed. Given the poor predictive value of genetic biomarkers in glioblastoma, we are conducting 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 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 will be 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 will be performed on PDCs with 28 drugs used for the treatment of solid tumors and hematological malignancies. Based on the cytotoxic activity of these drugs, as quantified by relative viability based on adenosine triphosphate levels, a molecular tumor board will recommend a personalized treatment regimen.RESULTS: 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.TRIAL REGISTRATION: The ATTRACT trial is registered under the ID NCT06512311 (https://clinicaltrials.gov/study/NCT06512311).
UR - http://www.scopus.com/inward/record.url?scp=105004823826&partnerID=8YFLogxK
U2 - 10.1093/noajnl/vdaf056
DO - 10.1093/noajnl/vdaf056
M3 - Journal article
C2 - 40351832
SN - 2632-2498
VL - 7
SP - vdaf056
JO - Neuro-Oncology Advances
JF - Neuro-Oncology Advances
IS - 1
M1 - vdaf056
ER -