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. 2023 May 11:1–15. Online ahead of print. doi: 10.1038/s44222-023-00063-3

Table 1.

Clinical trials with patient-derived cancer organoids guiding treatment decisions

Organ system Cancer Identifiers Phase Country Drugs Implementation
Respiratory system Lung cancer, solid tumours NCT03778814 I China Biologics: TCR T cells Identification and engineering of tumour-responsive T cells using patient-specific tumour organoids followed by re-injection of TCR T cells into the patients
Gastrointestinal system Pancreatic cancer NCT04931394 III China Gemcitabine, 5-fluorouracil, paclitaxel, oxaliplatin, irinotecan PDOs of pancreatic cancer are tested for their sensitivity to first-line pancreatic cancer drugs; patients receive the chemotherapy regimen based on the test results
Advanced pancreatic cancer NCT04931381 III China Gemcitabine, 5-fluorouracil, paclitaxel, oxaliplatin, irinotecan PDOs of advanced pancreatic cancer are tested for their sensitivity to first-line pancreatic cancer drugs; patients receive the chemotherapy regimen based on the test results
Advanced rectal cancer NCT05352165 NA China Neoadjuvant therapy Clinical efficacy of personalized neoadjuvant therapy based on PDO chemosensitivity combined with standard long-term radiotherapy is compared with efficacy of standard whole-course neoadjuvant therapy
Abdominal tumours NCT05378048 II Hong Kong PDO-guided treatment using standard-of-care treatments A multidisciplinary tumour board reviews the drug screen results from PDOs and genome-guided drug screening and chooses the treatment regimen accordingly
Mammary glands Breast cancer NCT04450706 NA USA Docetaxel, cyclophosphamide, adriamycin, methotrexate, 5-fluorouracil, paclitaxel Treatment decisions are based on results from PDOs grown from breast cancer biopsies plus genome sequencing
Breast cancer NCT05177432 I Singapore 10–12 anticancer drugs (alpelisib, trastuzumab-emtansine and others not specified) PDOs are exposed to 10–12 anticancer drugs and a table for treatment sensitivity is obtained; results will be reviewed by an expert panel to decide on the most suitable anticancer drug treatment
Urinary system Bladder cancer NCT05024734 II Switzerland Epirubicin, mitomycin, gemcitabine, docetaxel Generation of PDOs and in vitro drug sensitivity testing to guide clinical decision-making
Others Head and neck squamous cell carcinoma NCT04279509 NA Singapore 5-Fluorouracil, carboplatin, cyclophosphamide, docetaxel, doxorubicin, gemcitabine, irinotecan, oxaliplatin, paclitaxel and vinorelbine, etoposide, ifosfamide, methotrexate, pemetrexed and topotecan Generation of PDOs followed by a 10-drug panel screening and selection of chemotherapy based on a standard rating scale; if more than one drug appears effective in PDOs, the most suitable drug based on patient comorbidities is selected
Solid tumours such as gastrointestinal and breast cancer NCT05381038 I and II Singapore Azacitidine plus docetaxel, azacitidine plus paclitaxel, azacitidine plus irinotecan Generation of PDOs followed by drug screening and selection, and artificial intelligence-guided dosing modulation

Clinical trials are as listed on ClinicalTrials.gov. NA, not applicable; PDO, patient-derived organoid; TCR, T cell receptor.