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. 2020 Jul 7;11(8):2279–2290. doi: 10.1111/1759-7714.13542

Figure 4.

Figure 4

Heat map of drug response in Pptient‐derived organoids (PDOs). (a) The sensitivity to EGFR‐TKIs was analyzed in P1, P6, and P11, which harbored EGFR mutations (Inline graphic) EGFR L858R, and (Inline graphic) EGFR EX20ins. (b) The chemotherapeutic sensitivity was analyzed in P1, P6, and P11 (Inline graphic) EGFR L858R, and (Inline graphic) EGFR EX20ins. (c) Drug sensitivity screening was performed in P9, which harbored a KRAS mutation, using EGFR‐TKIs (Inline graphic) Afatinib, (Inline graphic) Erlotinib, (Inline graphic) Gefitinib, (Inline graphic) Icotinib, (Inline graphic) Neratinib, and (Inline graphic) Osimertinib and chemotherapy drugs (Inline graphic) Methotrexate, (Inline graphic) Cytarabine, (Inline graphic) Cisplatin, (Inline graphic) Carboplatin, (Inline graphic) Docetaxel, (Inline graphic) Etoposide, (Inline graphic) Gemcitabine, (Inline graphic) Irinotecan, (Inline graphic) Paclitaxel, (Inline graphic) Pemetrexed, (Inline graphic) Topotecan, (Inline graphic) Vincristine, (Inline graphic) Vinorelbine, and (Inline graphic) Cephalomannine. EGFR‐TKI, epidermal growth factor receptor tyrosine kinase inhibitor; PDO, patient‐derived organoid.