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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: Cancer Discov. 2021 Feb 9;11(6):1424–1439. doi: 10.1158/2159-8290.CD-20-0564

Table 2.

Actionable Alteration and Inhibitor Recommendations

Total N (%) Cohort 1: Relapsed/Refractory N (%) Cohort 2: Newly Diagnosed N (%)
N 153 101 52
Actionable Alteration Identified [90% CI]* 116 (76) [69-81] 77 (77) [69-84] 39 (74) [62-83]
Alteration Tier
 1 16 (14) 9 (11) 7 (18)
 2 6 (4) 6 (8) 0 (0)
 3 72 (62) 46 (56) 26 (68)
 4 7 (6) 5 (6) 2 (5)
 5 16 (14) 13 (16) 3 (8)
Additional Recommendation 3 (2) 3 (3) 0 (0)
Recommended Inhibitor Target [90% CI]** 114 (75) [68-80] 77 (76) [68-83] 37 (71) [59-81]
 MEK 62 (41) 39 (39) 23 (44)
 DOT1L/Menin 23 (15) 11 (11) 12 (23)
 FLT3 14 (9) 9 (12) 5 (9)
 MTOR 13 (8) 9 (9) 4 (8)
 JAK1/2 14 (9) 10 (10) 4 (8)
 JAK3 1 (1) 1 (1) 0 (0)
 WEE1 6 (4) 5 (5) 1 (2)
 HDAC 5 (3) 4 (4) 1 (2)
 ABL 5 (3) 5 (5) 0 (0)
 Gamma Secretase 4 (3) 2 (2) 2 (4)
 IDH1 4 (3) 2 (2) 2 (4)
 CDK4/6 3 (2) 2 (2) 1 (2)
 KIT 3 (2) 0 (0) 3 (6)
 PI3K 3 (2) 3 (3) 0 (0)
 TP53 2 (1) 1 (1) 1 (2)
 AKT 2 (1) 2 (2) 0 (0)
 BCL2 2 (1) 2 (2) 0 (0)
 BRAF 2 (1) 0 (0) 2 (4)
 CRM1 2 (1) 1 (1) 1 (2)
 SRC 2 (1) 2 (2) 0 (0)
 PDGFRB 1 (1) 1 (1) 0 (0)
 CXCR4 1 (1) 1 (1) 0 (0)
*

One patient had an actionable mutation found, but the patient died prior to having a treatment recommendation sent (case 100) and one patient had a BCR-ABL1 fusion identified but was already being treated with dasatinib so no additional recommendation was provided (case 90).

**

Patients may have had multiple recommended inhibitors.

Additional features of interest added retrospectively based on targetability during the course of the clinical trial (ex. TP53, CDKN2A)