Patient Registry Provides Unique Insight Into Myeloproliferative Neoplasms

The myMPN Patient Registry—the first patient-focused registry in the field of MPNs—has collected data from 744 patients since its creation by the MPN Research Foundation in September 2017. An analysis of this data, presented at the recent American Association for Cancer Research 2019 Annual Meeting, sheds light on the disease-related events, bone marrow biopsies, symptom reporting, and other patient data collected thus far and how it will impact future MPN research.