Table 4.
Topic of Study | Drug/Targets | Outcome | Reference |
---|---|---|---|
Establishment of PDO biobank from 10 NSCLC patients for drug screening | Natural compounds (chelerythrine chloride, cantharidin, harmine, berberine, betaine) |
Identified anticancer activity of natural compounds (chelerythine chloride, cantharidin, harmin) on both PDOs and cell lines. | [127] |
Validation of NSCLC PDOs for predicting treatment response | 26 anti-cancer drugs | PDOs retained the histological and genetic characteristics of the primary tumors. The in vitro response to drug screening with PDOs highly correlated with the mutation profiles in the primary tumor. |
[141] |
Evaluation of anticancer agents using PDOs with squamous and adenosquamous lung cancers | 78 anticancer agents including molecular target drugs, immune-checkpoint inhibitors | In vitro assay systems using PDOs were suitable for evaluating molecular targeted drugs. | [142] |
Establishment of biobank of 80 LCOs for drug screening | Targeted therapies including erlotinib, crizotinib, olaparib | Drug responses in LCOs correlated with genomic alterations | [19] |
Establishment of 12 PDOs from lung adenocarcinoma | 24 anti-cancer drugs | The drugs with the same targets displayed reproducible sensitivity patterns among organoid lines | [143] |