Evidence map›Paper›PMID 40646417›Full record

ReviewCurrent hematologic malignancy reports2025

Highlights from MPN Asia 2025: Advances in Molecular Pathogenesis and Therapeutic Strategies in Myeloproliferative Neoplasms.

Prithviraj Bose, Zhijian Xiao, Hans C Hasselbalch, Josef T Prchal, Minghui Duan, Abdulraheem Yacoub, Raajit Rampal, Jean-Jacques Kiladjian, Gabriela S Hobbs, Tsewang Tashi and 11 more

Abstract readReview
In one paragraph

Review in Current hematologic malignancy reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Prithviraj BoseDepartment of Leukemia, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. PBose@mdanderson.org.
Zhijian XiaoInstitute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Hans C HasselbalchDepartment of Hematology, Zealand University Hospital, Vestermarksvej 7-9, Roskilde, Denmark.
Josef T PrchalUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Minghui DuanDepartment of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Abdulraheem YacoubHematologic Malignancies and Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, USA.
Raajit RampalCenter for Hematologic Malignancies, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Jean-Jacques KiladjianINSERM U1131, Hopital Saint-Louis, Paris, France.
Gabriela S HobbsDepartment of Medical Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Tsewang TashiUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Kazuya ShimodaDivision of Hematology, Diabetes and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki-city, Miyazaki, Japan.
Keita KiritoDepartment of Hematology and Oncology, University of Yamanashi, Yamanashi, Japan.
Harinder GillDepartment of Medicine, School of Clinical Medicine, LKS Faculty of Medicine, the University of Hong Kong, Hong Kong, China.
Hsin-An HouDivision of Hematology, Department of Internal Medicine, Division of General Medicine, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Sung-Eun LeeDepartment of Hematology, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, Republic of Korea.
Jian HuangThe first Affiliation Hospital, Zhejiang University Medical School, Hangzhou, Zhejiang, China.
Bing LiUniversity of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Albert QinPharmaEssentia Corporation, Taipei, Taiwan.
Lennex Hsueh-Lin YuPharmaEssentia Corporation, Taipei, Taiwan.
John O MascarenhasTisch Cancer Institute, Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ruben A MesaLevine Cancer Institute, Cancer Programs, Atrium Health, Wake Forest University School of Medicine, Charlotte, NC, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purpose of reviewThis report summarizes key insights from the 8th Annual International Symposium on Myeloproliferative Neoplasms (MPN Asia 2025). The symposium brought together global experts to discuss advancements in MPN biology, diagnostics, and therapeutics, with a focus on emerging molecular understanding, novel treatment strategies and real-world data. RECENT

findingsMolecular profiling has become essential in MPN risk stratification and therapeutic decision-making. High-risk mutations (e.g., ASXL1, TP53) and inflammatory pathways (e.g., IL-17, NF-κB) were shown to correlate with disease progression and transformation. Interferon-based therapy is increasingly used in younger, low-risk, or treatment-naïve patients, and is also being investigated in myelofibrosis and essential thrombocythemia. Ropeginterferon alfa-2b, a novel interferon-based therapy, demonstrated durable clinical efficacy in polycythemia vera. Its high initial-dose and accelerated titration (HIDAT) regimen led to fast achievement of complete hematologic response, rapid reductions in JAK2V617F allele burden, and high complete molecular response rate. Combination regimens involving ruxolitinib and agents such as pelabresib, selinexor, and interferon showed potential for enhanced efficacy. Population-based studies from Asia contributed regional epidemiological and treatment data, reinforcing the role of real-world evidence. Modern prognostic models such as MIPSS70+ v2.0 and GIPSS were discussed for more precise risk prediction. Preliminary findings also suggest ropeginterferon alfa-2b may be a safe option during pregnancy. MPN Asia 2025 highlighted the growing role of molecular diagnostics and targeted therapeutics in the management of MPNs. Ropeginterferon alfa-2b has emerged as a therapeutic potential across the MPN spectrum. Its early use and personalized strategies are increasingly recognized. Real-world data and regional insights are shaping a more nuanced, globally informed approach to MPN care.

Indexed as

Myeloproliferative DisordersAsiaDisease ManagementHumansInterferon-alphaMutationInterferon-alpha

Identifiers

PMID40646417
PMCPMC12254180

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.