Results from a US modified Delphi consensus to define disease progression and disease modification in polycythemia Vera

Within 15 years of diagnosis, around 15% of polycythemia vera (PV) cases progress to post-PV myelofibrosis, and around 3% transform to acute myeloid leukemia within 10 years. Risk factors for disease progression include advanced age and the presence of certain acquired myeloid-relevant mutations. A better understanding of what defines disease progression in PV is essential when evaluating treatment options that enable disease modification and improved patient outcomes. A modified-Delphi method was used to convene a virtual steering group (SG) of seven US-based clinical physicians specializing in the management and treatment of PV. The group generated 41 consensus statements across six main domains. A survey was developed from these statements and shared with a broader panel of specialists, using a four-point Likert scale. The results were analyzed to determine the level of agreement for each statement. The consensus threshold was set at 75% agreement. A total of 61 responses were received from hematologist-oncologists (n = 56), oncologists (n = 3), and hematologists (n = 2). On analysis, 39/41 (95%) statements achieved consensus agreement, and 2/41 (5%) failed to achieve consensus. Consensus statements related to response assessment adjudication, treatment selection, and disease progression scored the highest, with 92% consensus among the wider panel. Based on the consensus, the SG agreed on a set of recommendations for defining disease progression and disease modification in PV. These recommendations aim to improve understanding of the disease course to support the development of more effective therapeutic strategies.

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Publication Details

Journal
Annals of Hematology
Published
2025-10-15
DOI
https://doi.org/10.1007/s00277-025-06641-2
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
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article

Results from a US modified Delphi consensus to define disease progression and disease modification in polycythemia Vera

Prithviraj Bose, Emily Nagler, Tsewang Tashi, Swapna Thota et al.
Annals of Hematology
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

Results from a US modified Delphi consensus to define disease progression and disease modification in polycythemia Vera

Prithviraj Bose, Emily Nagler, Tsewang Tashi, Swapna Thota, John O Mascarenhas, Raajit K. Rampal, Muhammad Sarfraz Nawaz
article en

Abstract

Within 15 years of diagnosis, around 15% of polycythemia vera (PV) cases progress to post-PV myelofibrosis, and around 3% transform to acute myeloid leukemia within 10 years. Risk factors for disease progression include advanced age and the presence of certain acquired myeloid-relevant mutations. A better understanding of what defines disease progression in PV is essential when evaluating treatment options that enable disease modification and improved patient outcomes. A modified-Delphi method was used to convene a virtual steering group (SG) of seven US-based clinical physicians specializing in the management and treatment of PV. The group generated 41 consensus statements across six main domains. A survey was developed from these statements and shared with a broader panel of specialists, using a four-point Likert scale. The results were analyzed to determine the level of agreement for each statement. The consensus threshold was set at 75% agreement. A total of 61 responses were received from hematologist-oncologists (n = 56), oncologists (n = 3), and hematologists (n = 2). On analysis, 39/41 (95%) statements achieved consensus agreement, and 2/41 (5%) failed to achieve consensus. Consensus statements related to response assessment adjudication, treatment selection, and disease progression scored the highest, with 92% consensus among the wider panel. Based on the consensus, the SG agreed on a set of recommendations for defining disease progression and disease modification in PV. These recommendations aim to improve understanding of the disease course to support the development of more effective therapeutic strategies.

Annals of HematologyVol. 104(10)
Memorial Sloan Kettering Cancer Center (US), The University of Texas MD Anderson Cancer Center (US), University of Tennessee Health Science Center (US), University of Utah (US), Scripps MD Anderson Cancer Center (US), University of Tennessee at Knoxville (US), Marian University - Indiana (US), Icahn School of Medicine at Mount Sinai (US)
Openalex Percentile: Top 60%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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