Abstract

Phylogeny of Wilms tumor?

Highlights

  • The paper by Cresswell et al (2016) addresses important issues in understanding the heterogeneous pathogenetic pathways in Wilms tumors and practical questions of how sensitive and specific is a tumor biopsy for identifying important genetic changes

  • If therapy is going to be based on the tumor genetics, we need a clear understanding of the pathogenetic pathways and the likelihood of identifying key prognostic/ diagnostic information in a tumor biopsy

  • The question for pediatric tumors, is how do steps occur at such a young age and are there fewer steps? One point to note is that small round blue cell tumors of childhood tend to be rapidly proliferative and time should be measured by cell cycles, rather than months and years

Read more

Summary

Introduction

The paper by Cresswell et al (2016) addresses important issues in understanding the heterogeneous pathogenetic pathways in Wilms tumors and practical questions of how sensitive and specific is a tumor biopsy for identifying important genetic changes. If therapy is going to be based on the tumor genetics, we need a clear understanding of the pathogenetic pathways and the likelihood of identifying key prognostic/ diagnostic information in a tumor biopsy. Wilms tumors though appear genetically heterogeneous, with some tumors showing few changes and others showing more changes as the current paper demonstrates (Cresswell et al, 2016).

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call