Abstract 2515: Preserving predictive power with minimal PDOs: Accelerated drug testing for personalized therapy in metastatic CRC

Abstract Patients with relapsed or metastatic colorectal cancer (CRC) face limited treatment options, significant side effects, and prolonged delays in identifying effective therapies. Patient-derived organoids (PDOs; HUB Organoids®) provide a clinically relevant platform that faithfully mirrors individual tumour biology, enabling personalised drug testing. However, conventional drug screening formats typically require several hundred organoids per well, limiting the feasibility of using PDOs to guide real-time treatment decisions at diagnosis or relapse. Translational speed is critical: in metastatic CRC, there is a narrow window to select effective therapy before disease progression or treatment-related toxicity occurs. Traditional preclinical models often take weeks to months, which is too slow to inform immediate patient care. To address this limitation, we developed an automated organoid-handling workflow using the Yamaha CELL HANDLER™ system, enabling precise transfer and image-based quantification while requiring far fewer organoids per well. Miniaturisation reduced input material by 96% (from 250 to 10 PDOs per well) compared to conventional screening. Drug sensitivity of PDOs measured using the miniaturised assay closely mirrored that of conventional screening (R=0.67-0.85, p<0.03). PDO responses in the miniaturised assay also correlated with patient outcomes, including progression-free survival (R = -0.85, p < 0.01). By combining automation, miniaturisation, and quantitative readouts, this platform preserves the predictive power of PDOs, drastically reduces the need for organoids, and shortens turnaround time. Citation Format: Yasmine Abouleila, Roel Verkerk, Mayke Doorn, Timo Voskuilen, Gakuro Harada, Masahiko Watanabe, Lidwien Smabers, Hideaki Kyan, Takahiko Kumagai, Yuichi Hikichi, Rene Overmeer, Jeanine Roodhart, Kiyotaka Matsuno, Carla S. Verissimo, Robert G. Vries, Sylvia F. Boj. Preserving predictive power with minimal PDOs: Accelerated drug testing for personalized therapy in metastatic CRC [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2515.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2515
Primary Topic
Cancer Cells and Metastasis
Type
article
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article

Abstract 2515: Preserving predictive power with minimal PDOs: Accelerated drug testing for personalized therapy in metastatic CRC

Yasmine Abouleila, Timo Voskuilen, Yuichi Hikichi, Takahiko Kumagai et al.
Cancer Research
Cancer Cells and Metastasis
article

Abstract 2515: Preserving predictive power with minimal PDOs: Accelerated drug testing for personalized therapy in metastatic CRC

Yasmine Abouleila, Timo Voskuilen, Yuichi Hikichi, Takahiko Kumagai, Hideaki Kyan, René Overmeer, Kiyotaka Matsuno, J. Roodhart, Sylvia F. Boj, Carla S. Verissimo, Mayke Doorn, Roel Verkerk, Masahiko Watanabe, Lidwien Smabers, Gakuro Harada, Robert G. Vries
article en

Abstract

Abstract Patients with relapsed or metastatic colorectal cancer (CRC) face limited treatment options, significant side effects, and prolonged delays in identifying effective therapies. Patient-derived organoids (PDOs; HUB Organoids®) provide a clinically relevant platform that faithfully mirrors individual tumour biology, enabling personalised drug testing. However, conventional drug screening formats typically require several hundred organoids per well, limiting the feasibility of using PDOs to guide real-time treatment decisions at diagnosis or relapse. Translational speed is critical: in metastatic CRC, there is a narrow window to select effective therapy before disease progression or treatment-related toxicity occurs. Traditional preclinical models often take weeks to months, which is too slow to inform immediate patient care. To address this limitation, we developed an automated organoid-handling workflow using the Yamaha CELL HANDLER™ system, enabling precise transfer and image-based quantification while requiring far fewer organoids per well. Miniaturisation reduced input material by 96% (from 250 to 10 PDOs per well) compared to conventional screening. Drug sensitivity of PDOs measured using the miniaturised assay closely mirrored that of conventional screening (R=0.67-0.85, p<0.03). PDO responses in the miniaturised assay also correlated with patient outcomes, including progression-free survival (R = -0.85, p < 0.01). By combining automation, miniaturisation, and quantitative readouts, this platform preserves the predictive power of PDOs, drastically reduces the need for organoids, and shortens turnaround time. Citation Format: Yasmine Abouleila, Roel Verkerk, Mayke Doorn, Timo Voskuilen, Gakuro Harada, Masahiko Watanabe, Lidwien Smabers, Hideaki Kyan, Takahiko Kumagai, Yuichi Hikichi, Rene Overmeer, Jeanine Roodhart, Kiyotaka Matsuno, Carla S. Verissimo, Robert G. Vries, Sylvia F. Boj. Preserving predictive power with minimal PDOs: Accelerated drug testing for personalized therapy in metastatic CRC [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2515.

Cancer ResearchVol. 86(7_Supplement)
Yamaha (Japan) (JP), University Medical Center Utrecht (NL)
Good health and well-being
Openalex Percentile: Top 28%
Cancer Cells and Metastasis
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