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. 2023 Mar 3;11(3):773. doi: 10.3390/biomedicines11030773

Table 1.

The use of organoids for chemotherapy sensitivity testing in TNBC.

Therapeutic Agents Dose Ranges/IC50 Values Main Results References
Circular RNA 1.17–8.24 μM Doxorubicin sensitivity increase [35]
Decitabine 100 nM DNMT protein level correlates
with decitabine efficacy
[36]
Docetaxel,
Epirubicin
Docetaxel dose: 1 nM
Epirubicin logIC50 values =  0.3728 μM, 26.7300 μM
Decreased TNBC
organoids’ viability
Consistency of clinical response
and response of tissue-derived organoids
[29,31]
Multiple Agents 20 μM–27.4 nM High patient-derived organoid pharmaco-phenotyping association with clinical outcomes and previous treatment responses
Patient-specific sensitivity predication for personalized therapy by patient-derived organoid pharmaco-phenotyping
[30]
MuV-U-Japan Multiplicity of infection = 0–10 Potent killing effect in chemotherapy-resistant TNBC patient-derived xenograft organoids [37]
Paclitaxel,
Romidepsin,
Trametinib
IC50 values = 10,500, 18,000 +/− 12.6,
6.5–24.9 μM
Organoid growth inhibition
High IC50 paclitaxel value in
TNBC patient-derived xenograft organoids
CD44 and E-cadherin downregulation
Enhanced apoptosis induction
after SYTL4 knockdown
[32,33,34]