The Classic Myeloproliferative Neoplasms
Optimizing Laboratory Testing for Hematologic Disorders Series
MPL Exon 10 Sequencing Studies: Background
October 2011
The final topic today regards MPL exon 10 sequencing studies. As background, MPL exon 10 mutations are relatively infrequent and have been identified in approximately 10% of primary myelofibrosis and about 5% of ET patients, while rarely being identified in PV and never in CML. MPL mutations are only rarely present with JAK2 mutations and, in general, MPL mutations are not associated with significant clinical findings or outcomes that would affect the clinical management of those patients.
Exon 10 Sequencing Studies: Background |
Jump to section:
- Introduction
- Optimizing Laboratory Testing for Hematologic Disorders Series
- Goals for Today's Presentation
- Example of a Recent MPN Referral
- Why Do We Have Test Utilization Issues?
- Why Do We Have Test Utilization Issues?
- So What Should We Do?
- WHO Classification
- Important Laboratory Assays in the MPNs
- JAK2 V617F Background
- JAK2 V617F Background
- Question #1 — JAK2 V617F
- JAK2 V617F
- JAK2 V617F at Mayo Clinic
- Conclusion #1 — JAK2 V617F
- JAK2 Exon 12 Sequencing Background
- Question #2 — JAK2 Exon 12 Sequencing
- JAK2 Exon 12 Sequencing: When Not to Use
- JAK2 Exon 12 Sequencing
- Conclusion #2 — JAK2 Exon 12 Sequencing
- MPL Exon 10 Sequencing Studies: Background
- Question #3 — MPL Exon 10 Sequencing
- MPL Exon 10 Sequencing: When to Use
- MPL Exon 10 Sequencing: When Not to Use
- MPL Exon 10 Sequencing
- Conclusion #3 — MPL Exon 10 Sequencing
- Roles of Other Assays in Classic MPN
- Summary
- Myeloproliferative Neoplasm: A Diagnostic Approach to Peripheral Blood Evaluation
- Myeloproliferative Neoplasm: A Diagnostic Approach to Bone Marrow Evaluation
- Implementing a Utilization Approach
- Questions


