Table 2.
Guideline recommendations for TP53 and IGHV analysis in clinical practice.
Society | Recommendation | Timing |
---|---|---|
iwCLL | ||
TP53 disruption | Always | Prior to treatment |
IGHV gene mutational status | Always | Prior to treatment |
BCSH | ||
TP53 disruption | Always | Prior to treatment |
IGHV gene mutational status | “Should be considered” | Prior to treatment |
NCCN | ||
TP53 disruption | Always | At diagnosis or prior to treatment 1 |
IGHV gene mutational status | Always | At diagnosis or prior to treatment |
ESMO | ||
TP53 disruption | Always | Prior to treatment |
IGHV gene mutational status | “Desirable” | Prior to treatment |
TP53 disruption includes both del17p by fluorescent in-situ hybridization and TP53 gene mutational analysis by either Sanger or next-generation sequencing. 1 In the case of analysis performed in early-stage disease under a “watch-and-wait” strategy or relapsed/refractory cases undergoing subsequent therapy, TP53 analysis should be repeated prior to treatment to assess effects of clonal evolution. Abbreviations: IGHV, immunoglobulin heavy chain variable gene; iwCLL, international workshop on chronic lymphocytic leukemia; BCSH, British committee for standards in haematology; NCCN, national comprehensive cancer network; ESMO, European society for medical oncology.