Yes, so during this session we discussed established markers like the IGHV gene mutation status, TP53 mutations and deletional 17p which are used today and included in the guidelines recommendation. So it’s important to do these markers and you should do them before the start of first treatment but also at subsequent rounds of treatment. We were also discussing other markers that are discussed like complex karyotype...
Yes, so during this session we discussed established markers like the IGHV gene mutation status, TP53 mutations and deletional 17p which are used today and included in the guidelines recommendation. So it’s important to do these markers and you should do them before the start of first treatment but also at subsequent rounds of treatment. We were also discussing other markers that are discussed like complex karyotype. This is a more complex marker that you can detect with traditional cytogenetics or with array technology so it appears that this marker is we still need to define it further so for the time being it’s recommended to be included in clinical studies but not in routine practice then we had other markers for instance the specific marker IGHV3-21 R110 mutation that seems to identify a proportion of cases with very poor outcome and we I would say that it’s still discussed we can see it’s a poor risk marker and it would be possible to detect it but we are still not ready to include it.
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