Patient-derived tumor organoids for new drug development: promises and challenges.
The development of antitumor drugs is affected by various unfavorable factors, including long cycles of research and development, large differences in drug efficacy in vivo, and efficacy differences i
APA
He M, Wu Y, et al. (2026). Patient-derived tumor organoids for new drug development: promises and challenges.. Investigational new drugs, 44(1), 90-102. https://doi.org/10.1007/s10637-026-01605-3
MLA
He M, et al.. "Patient-derived tumor organoids for new drug development: promises and challenges.." Investigational new drugs, vol. 44, no. 1, 2026, pp. 90-102.
PMID
41689692
Abstract
The development of antitumor drugs is affected by various unfavorable factors, including long cycles of research and development, large differences in drug efficacy in vivo, and efficacy differences in individuals. Patient-derived tumor organoids (PDTOs), a novel preclinical model in cancer research, are three-dimensional microstructures differentiated from stem cells, with the capability of self-organizing into micro-organs that resemble the original tumor tissues. They have been demonstrated to faithfully recapitulate the biological and molecular features of the original tumor while preserving the tumor heterogeneity. Recently, PDTOs show great potential in drug screening and new drug development. In this review, we overviewed the types of organoids, application of PDTOs in developing new drugs, as well as their challenges and opportunities to provide powerful insights into drug development.
MeSH Terms
Humans; Organoids; Drug Development; Neoplasms; Antineoplastic Agents; Animals; Drug Screening Assays, Antitumor
같은 제1저자의 인용 많은 논문 (5)
- Beyond Rationality: Information Overload and Biased Perceptions of Lung Cancer Screening Among Middle-Aged Adults.
- Quantification of Antibody-Drug Conjugate Targets in Head and Neck Squamous Cell Carcinoma.
- In situ reprogramming of tumor associated macrophages with versatile nano-epigenetic inhibitor for lung cancer therapy.
- Evaluating the impact of reader experience on PI-RADS 3 of version 2.1 scoring concordance in multiparametric prostate MRI: a single-center analysis.
- A two-step scoring model incorporating visceral-to-subcutaneous fat ratio and systemic immunoinflammatory index for predicting cytokine release syndrome severity in patients with gastric cancer receiving Claudin18.2-targeted CAR-T cell therapy.