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RESEARCH PAPER ANALYSIS

Adolescent and Young Adult versus Older Adult Philadelphia-Negative Myeloproliferative Neoplasms: A Single-Center Experience from the MENA Region.

This single-center retrospective MENA-region study of 220 patients reports that adolescents and young adults with Philadelphia-negative myeloproliferative neoplasms differed from older adults in risk classification, molecular profiles, and thrombotic phenotype, but not overall survival.

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PMID42602648
JournalJournal of blood medicine
Publication Date2026-08-10
Ingested2026-08-17 09:15 AM
EXECUTIVE SUMMARY

What the AI sees

This single-center retrospective MENA-region study of 220 patients reports that adolescents and young adults with Philadelphia-negative myeloproliferative neoplasms differed from older adults in risk classification, molecular profiles, and thrombotic phenotype, but not overall survival.

WHY IT MATTERS

Research significance

The study provides observational evidence of age-associated clinical and molecular differences; it supports the hypothesis, but does not demonstrate, that AYA-specific risk assessment or treatment-selection strategies could improve management of Philadelphia-negative MPNs.

ABSTRACT

Source abstract

BACKGROUND: Philadelphia-negative myeloproliferative neoplasms (MPNs), including essential thrombocythaemia (ET), polycythaemia vera (PV), and myelofibrosis (MF), usually affect older adults, but a subset occurs in adolescents and young adults (AYA). Regional age-stratified data remain limited. METHODS: We retrospectively studied Philadelphia-negative MPN patients managed at the National Center for Cancer Care and Research from 2014 to 2024. Patients were classified as AYA (15-39 years) or older adults (≥40 years). Clinical, laboratory, molecular, thrombotic, bleeding, transformation, and survival outcomes were analyzed by subtype. Risk categories followed institutional disease-specific practice; analyses were descriptive and unadjusted. RESULTS: The cohort included 220 patients: 79 ET, 47 MF, and 94 PV; 76 (34.5%) were AYA. Low-risk disease predominated in AYA ET (p<0.001) and PV (72.4% vs 35.4%; p=0.002), partly reflecting age-based risk definitions. In ET (molecular n=30 vs 49), CALR was 16/30 (53.3%) versus 19/49 (38.8%) and JAK2 was 6/30 (20.0%) versus 21/49 (42.9%); MPL, triple-negative, and unavailable categories were 2, 4, and 2 versus 2, 6, and 1, respectively. In MF (n=11 vs 36), JAK2 was 4 (36.4%) versus 18 (50.0%), CALR 4 (36.4%) versus 10 (27.8%), MPL 0 versus 2 (5.6%), triple-negative 1 (9.1%) versus 3 (8.3%), and unavailable data 2 (18.2%) versus 3 (8.3%). In PV (n=29 vs 65), JAK2 V617F was 28 (96.6%) versus 63 (96.9%) and JAK2 exon 12 was 1 (3.4%) versus 2 (3.1%). Overall survival did not differ by age. CONCLUSION: AYA patients with Philadelphia-negative MPNs demonstrated age-related differences in risk classification, molecular profile, and thrombotic phenotype, while overall survival was comparable to older adults. Larger prospective multicenter studies are warranted.

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PATIENT-FRIENDLY SUMMARY

Adolescent and Young Adult versus Older Adult Philadelphia-Negative Myeloproliferative Neoplasms: A Single-Center Experience from the MENA Region.

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