Skip to main content
. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Clin Cancer Res. 2018 Sep 26;25(1):346–357. doi: 10.1158/1078-0432.CCR-18-1129

Figure 1. DISARM design and validation.

Figure 1.

(A) Adapted IC50 data (15) for NSCLC cell lines treated with the EGFR inhibitors erlotinib and osimertinib, the latter of which is effective in instances of EGFR T790M erlotinib resistance mutations. (C) DISARM-generated 2×2 plot for erlotinib (reference) and osimertinib (candidate) pair, in which DISARM accurately selects osimertinib as an effective agent in erlotinib-resistant NSCLC. Each black dot in 2×2 plot indicates a specific cell line. (D) Similarly, adapted IC50 data for CML cell lines (16) treated with the BCR-ABL inhibitors dasatinib (reference) and ponatinib (candidate), the latter of which is an effective therapy in instances of BCR-ABL T315I resistance mutations. (E) DISARM correctly selects ponatinib as an effective therapy for dasatinib-resistant CML. (B-E) IC50 and log10(IC50) values are expressed in nanomolar (nM) concentration.