Table 1.
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.