Figure 1.
Gene mutations in pretreatment and relapse MM samples detected by WES. (A) Number of mutations at diagnosis (gray) and acquired mutations in serial relapse time points (red, relapse 1; yellow, relapse 2; green, relapse 3). Each bar shows the total number of mutations at the respective time point (D, diagnosis; R, relapse) in individual patients. Treatments with dexamethasone, immunomodulatory drugs (IMiD), bortezomib and melphalan before the acquisition of the sample are indicated below. (B) Distribution of mutations (number (%)) detected at diagnosis and in relapse samples. Mutations present only at diagnosis are color-coded in blue, mutations present at both time points in gray, and mutations present only at relapse in red. Dashed lines indicate the proportion of mutations with a VAF increase >10% at relapse. (C) Recurrent gene mutations at diagnosis and relapse. Each column represents 1 patient. For each gene, the presence of a mutation (color-coded in red; dark gray indicates no mutations was detected) at different time points is indicated in subsequent rows. On the right-hand side, the frequency of mutated patients at diagnosis and at relapse is given. UPN, unique patient number.

Gene mutations in pretreatment and relapse MM samples detected by WES. (A) Number of mutations at diagnosis (gray) and acquired mutations in serial relapse time points (red, relapse 1; yellow, relapse 2; green, relapse 3). Each bar shows the total number of mutations at the respective time point (D, diagnosis; R, relapse) in individual patients. Treatments with dexamethasone, immunomodulatory drugs (IMiD), bortezomib and melphalan before the acquisition of the sample are indicated below. (B) Distribution of mutations (number (%)) detected at diagnosis and in relapse samples. Mutations present only at diagnosis are color-coded in blue, mutations present at both time points in gray, and mutations present only at relapse in red. Dashed lines indicate the proportion of mutations with a VAF increase >10% at relapse. (C) Recurrent gene mutations at diagnosis and relapse. Each column represents 1 patient. For each gene, the presence of a mutation (color-coded in red; dark gray indicates no mutations was detected) at different time points is indicated in subsequent rows. On the right-hand side, the frequency of mutated patients at diagnosis and at relapse is given. UPN, unique patient number.

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