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. 2019 May 13;12(7):951–958. doi: 10.1016/j.tranon.2019.04.001

Table 2.

Viability of melanoma lymph node metastases and PDXs analyzed ex vivo after treatment with Vemurafenib (2 μM)

Patient No. Mutation Relative viability (% of control)1
Lymph node PDX passage2,3
Lowest Highest
Melmet-334 BRAF n.a.* 52 (4) - (n.a.)**
Melmet-347 BRAF 31 64 (1) 13 (3)
Melmet-350 BRAF 59 - (0) - (1)
Melmet-351 BRAF n.a. 57 (2) 56 (6)
Melmet-356 BRAF 102 - (0) - (4)
Melmet-363 BRAF 52 43 (7) 28 (8)
Melmet-376 BRAF 52 33 (2) 43 (6)
Melmet-380 BRAF 16 26 (0) 42 (3)
Melmet-381 BRAF 30 87 (4) 11 (7)
Melmet-382 BRAF 35 17 (2) 18 (5)
Melmet-389 BRAF n.a. 61 (0) 12 (6)
Melmet-393 BRAF n.a. 30 (3) 20 (6)
Melmet-358 NRAS 132 86 (0) 107 (5)
Melmet-365 NRAS 201 122 (1) 116 (5)
Melmet-367 NRAS 91 118 (7) n.a. (n.a.)
Melmet-369 NRAS 74 169 (0) 271 (3)
Melmet-388 NRAS 89 67 (0) 125 (7)
Melmet-256 Wt/Wt 83 86 (0) 80 (7)
Melmet-370 Wt/Wt 70 98 (1) 103 (10)
Melmet-374 Wt/Wt n.a. 79 (3) 103 (5)
Melmet-404 Wt/Wt 116 77 (0) 103 (1)

1 Percentage survival.

2 Number of passages in parentheses.

3 PDX for Melmet-350, -356 not analyzed due to control sample not growing.

* n.a. = Not analyzed due to limited tumor material available.

** Only one PDX passage analyzed.